View ValuationCorMedix 향후 성장Future 기준 점검 2/6CorMedix은 연간 수입과 매출이 각각 8.4%와 12.4% 증가할 것으로 예상되고 EPS는 연간 2.6%만큼 감소할 것으로 예상됩니다.핵심 정보8.4%이익 성장률-2.61%EPS 성장률Pharmaceuticals 이익 성장14.4%매출 성장률12.4%향후 자기자본이익률n/a애널리스트 커버리지Good마지막 업데이트07 May 2026최근 향후 성장 업데이트공지 • Mar 05CorMedix Inc. Reiterates Earnings Guidance for the Year 2026CorMedix reiterated earnings guidance for the year 2026. For the year, company reiterated previously established guidance for 2026, including net revenue of between $300 and $320 million .공지 • Nov 12+ 1 more updateCorMedix Inc. Raises Earnings Guidance for the Year Ending December 31, 2025CorMedix Inc. raised earnings guidance for the year ending December 31, 2025. For the year, the company raises its full-year 2025 pro forma net revenue guidance to a range of $390 to $410 million.공지 • Aug 07CorMedix Inc. Provides Earnings Guidance for the Full Year 2025CorMedix Inc. provided earnings guidance for the full year 2025. For the year, the company expects Pro Forma 2025 Revenue: $305 million – $335 million.공지 • Jun 24CorMedix Inc. Increases Net Sales Guidance of Second Quarter 2025CorMedix Inc. announced that as a result of this new customer implementation and other positive business developments, CorMedix is increasing its second quarter 2025 net sales guidance from the previously communicated $31 million to a range of $35 million to $40 million.공지 • May 06CorMedix Inc. Revises Sales Guidance for the First Half of 2025CorMedix Inc. revised sales guidance for the first half of 2025. The company expected to be at the high-end of the previously announced first half net sales guidance of $62 million to $70 million, based on latest order trends and inventory tracking with current purchasing customers.공지 • Apr 08CorMedix Inc. Raises Financial Guidance for First Half of 2025CorMedix Inc. raised financial guidance for first half of 2025. Since providing initial guidance, the Company received larger than expected orders during the final week of March, and has also obtained additional visibility into inventory levels on hand at some of its current purchasing customers. Based on this new information, CorMedix is increasing its first half 2025 guidance for Net Sales to existing purchasing customers to a revised range of $62 million to $70 million.모든 업데이트 보기Recent updates내러티브 업데이트 • May 11CRMD: Mixed Research And Phase III Success Will Support Undervalued SharesCorMedix's analyst price target has changed to $15.00 from $14.57 as analysts update their models for revenue growth, profit margins, discount rate and future P/E assumptions following mixed recent Street research. Analyst Commentary Recent research on CorMedix reflects a mix of optimism and caution as analysts adjust their valuation frameworks and expectations for execution.공지 • May 05CorMedix Inc. to Report Q1, 2026 Results on May 14, 2026CorMedix Inc. announced that they will report Q1, 2026 results Pre-Market on May 14, 2026내러티브 업데이트 • Apr 30CRMD is trading at 5.9x trough-year EBITDA with the market ascribing near-zero value to two near-term pipeline eventsWith ReSPECT Phase III positive this week, CRMD has resolved its single largest binary risk and now trades at a 63% discount to base case intrinsic value with a bear case floor only 8% below current price, as the REZZAYO prophylaxis sNDA path, DefenCath TPN pipeline, and post-TDAPA revenue recovery converge toward a 2027 inflection that the $7 stock price is not remotely reflecting.공지 • Apr 29Cormedix Therapeutics Announces Positive Topline Results from Phase III Respect Trial Assessing Rezzayo for the Prophylaxis of Invasive Fungal Diseases in Allogeneic Hematopoietic Stem Cell Transplantation PatientsCorMedix Therapeutics announced positive Phase III topline results from the global ReSPECT clinical trial evaluating REZZAYO (rezafungin for injection) for prophylaxis of invasive fungal diseases (IFDs) in adult patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT). The ReSPECT Phase III study, one of the largest anti-fungal multicenter, randomized, double-blind studies evaluated the efficacy and safety of once weekly rezafungin (rezafungin acetate) compared with a standard antimicrobial regimen (SAR) for the prophylaxis of invasive fungal diseases, including infections caused by Candida, Aspergillus, and Pneumocystis, in adults undergoing allogeneic HSCT. Patients undergoing allogeneic blood and marrow transplantation face prolonged periods of immunosuppression and routinely require extended antifungal prophylaxis, representing a setting where differentiated dosing, improved side effect profile, and reduced DDI is beneficial, and comparable efficacy is expected. The ReSPECT study met its primary endpoint for FDA and EMA for fungal-free survival at Day 90 showing non-inferiority vs. SAR, with 60.7% fungal-free survival at Day 90 for rezafungin compared to 59.0% for standard antimicrobial regimen. This demonstrates that rezafungin’s differentiated pharmacokinetics/pharmacodynamics (PK/PD) profile was comparable to the standard antimicrobial regimen (SAR) in reducing the incidence of invasive fungal infections in a high-risk patient population. Rezafungin was well tolerated, with a safety profile showing a favorable benefit/risk profile for immunocompromised patients. The Phase III study topline results demonstrated comparable efficacy against invasive infections from candida, aspergillus and pneumocystis in both therapeutic arms, as well as comparable mortality. In addition, results showed a favorable profile in multiple secondary endpoints, most notably treatment emergent adverse events leading to dose reduction, interruption or withdrawal of study drug, and treatment emergent adverse events leading to study discontinuation. This clinical trial has been sponsored by Mundipharma. Mundipharma has commercial rights to rezafungin outside the U.S. Mundipharma has partnered with Melinta Therapeutics, LLC, a wholly owned subsidiary of CorMedix for US distribution of rezafungin. The companies anticipate a pre-NDA submission meeting with FDA in the coming months, followed by a target submission of a supplemental New Drug Application (sNDA) to the FDA in Second Half 2026 based on the ReSPECT results. Rezafungin is a next generation echinocandin approved for the treatment of candidemia and invasive candidiasis in adults. Invasive candidiasis continues to be an area of significant unmet need, especially for critically ill patients in hospitals and patients with compromised immune systems. Despite a number of available treatments, the mortality rate for patients with invasive candidiasis is as high as 40%. Rezafungin has been studied for the prophylaxis of invasive fungal diseases in adults undergoing allogeneic HSCT. CorMedix estimates that the potential US market opportunity for REZZAYO in prophylaxis exceeds $2 billion, based on internal analyses and assumptions. These estimates are forward-looking statements and are subject to regulatory approvals, clinical practice considerations, and market adoption. Rezafungin has orphan drug exclusivity through 2035 and patent coverage through 2038 in the U.S. REZZAYO is a Registered Trademark of Mundipharma, used under license by Melinta Therapeutics LLC, a wholly owned subsidiary of CorMedix in the US.내러티브 업데이트 • Apr 23CRMD: Reaffirmed 2026 Outlook And Buyback Plan Will Support Undervalued SharesAnalysts have trimmed their 12 month price target on CorMedix to $13 from $15, reflecting updated views on revenue growth, profitability, and appropriate future P/E levels for the stock. Analyst Commentary Recent price target revisions to US$13 from US$15 sit alongside continued positive ratings, which gives a mixed message for investors.공지 • Apr 21CorMedix Inc., Annual General Meeting, Jun 23, 2026CorMedix Inc., Annual General Meeting, Jun 23, 2026.내러티브 업데이트 • Apr 06CRMD: Investor Day Will Reframe Lower Guidance And Support Undervalued OutlookNarrative Update on CorMedix Analysts have reduced their blended price targets on CorMedix by several dollars to a range of roughly $13 to $16, citing updated company revenue guidance that is materially below prior Street expectations, especially for DefenCath in 2026 and 2027. Analyst Commentary Street research on CorMedix has shifted toward lower valuation targets after the company issued revenue guidance for 2026 and 2027 that sits well below prior expectations, particularly for DefenCath.Seeking Alpha • Apr 02CorMedix: Waiting On Phase III ReSPECT For A Further Re-Rating (Upgrade)Summary CorMedix Inc. is upgraded to Hold, with near-term upside tied to the pivotal Phase III ReSPECT trial for Rezzayo in Q2 '26. CRMD's FY25 saw strong profitability: $163.1M net income, $401.3M pro forma revenue, and $77.2M adjusted EBITDA, aided by the Melinta acquisition. CRMD stock trades at discounted multiples (8.43x P/E, 4.38x EV/EBITDA), reflecting execution risk and conservative growth assumptions despite robust cash flow. The ReSPECT trial could unlock a $2B prophylaxis market and drive a CRMD stock valuation re-rating if results are positive. Read the full article on Seeking Alpha새 내러티브 • Apr 02CRMD is trading at 5.9x trough-year EBITDA with the market ascribing near-zero value to two near-term pipeline eventsInvestment Thesis DefenCath's regulatory moat (only FDA-approved antimicrobial CLS in the U.S., NCE+GAIN exclusivity through 2033, composition patent to 2042) is intact and the 72% real-world CRBSI reduction is standard-of-care quality data; the TDAPA pricing step-down is a commercial mechanics event, not a competitive displacement event The stock at $7.02 prices in approximately the bear case ($6.54), meaning investors are effectively receiving the REZZAYO prophylaxis Phase III binary and the DefenCath TPN pipeline for free — an unusual asymmetry for a cash-flow-positive commercial pharma company Operating cash flow of $175M in FY2025 and $148.5M in cash provides full self-funding of pipeline without dilution risk, and the $75M buyback at current prices represents management's explicit capital allocation conviction about intrinsic value The Melinta acquisition was well-priced ($30M goodwill on $391M identified intangibles) and adds an annualizing $130M+ revenue stream with shared call points that provide SG&A leverage as the combined platform scales Post-TDAPA recovery in 2027 (3x–5x higher add-on payment vs. H2 2026 per management, plus Medicare Advantage contracting upside not in guidance) provides a clearly identified catalyst path back to re-rating independent of pipeline success Risk Considerations ReSPECT Phase III failure (data Q2 2026) would eliminate ~$221M of base case rNPV, trigger impairment of the $143M IPR&D intangible, and likely reset the stock to the $5.60 52-week low or below — this is the primary binary risk and is near-term Customer concentration at 79% revenue from three accounts is structurally dangerous; any publicly announced reduction in DefenCath orders from a major dialysis organization would be a material negative event with little warning The Q4 GAAP EPS miss ($0.16 vs.내러티브 업데이트 • Mar 22CRMD: Investor Day Will Clarify Lower Guidance And Highlight Perceived UpsideAnalysts have trimmed CorMedix price targets by $2 to $9, with recent cuts such as $20 to $16 and $15 to $13, reflecting updated views on DefenCath revenue guidance and the company outlook shared in recent research notes. Analyst Commentary Recent research reflects a reset in expectations for CorMedix as analysts align their models with the latest DefenCath revenue guidance and management commentary.내러티브 업데이트 • Mar 08CRMD: Investor Day Reset On Lower Guidance Will Highlight Undervalued UpsideNarrative Update on CorMedix The analyst price target for CorMedix has been trimmed from about $14.86 to roughly $14.57. Analysts are recalibrating their models in light of lower revenue growth and margin expectations, along with a more conservative view on long term DefenCath contribution, as reflected in recent target cuts from $20 to $16, $15 to $13, and other reductions across the Street.공지 • Mar 05CorMedix Inc. Reiterates Earnings Guidance for the Year 2026CorMedix reiterated earnings guidance for the year 2026. For the year, company reiterated previously established guidance for 2026, including net revenue of between $300 and $320 million .공지 • Mar 02CorMedix Inc. to Report Q4, 2025 Results on Mar 05, 2026CorMedix Inc. announced that they will report Q4, 2025 results Pre-Market on Mar 05, 2026내러티브 업데이트 • Feb 21CRMD: Investor Day Will Reframe Lower Guidance And Support Undervalued ThesisAnalysts have trimmed their average price targets on CorMedix by a mid single digit dollar amount, citing the company's new FY26 and 2027 DefenCath revenue guidance, which sits well below prior Street expectations, as a key driver of their revised views. Analyst Commentary Bullish Takeaways Bullish analysts still see room for upside even with price targets trimmed, suggesting they view the lower guidance as already influencing valuation assumptions.내러티브 업데이트 • Feb 07CRMD: Investor Day And New Revenue Guidance Will Shape Bullish CaseAnalysts have trimmed their price targets on CorMedix, with our fair value estimate moving from US$16.86 to US$14.86 as they factor in lower revenue growth and profit margin assumptions, despite a higher future P/E multiple. Analyst Commentary Bullish Takeaways Bullish analysts still see upside potential in CorMedix shares, pointing to the higher future P/E multiple being used in their models as a sign that they are willing to ascribe a premium to the company despite reduced revenue assumptions.분석 기사 • Feb 06CorMedix Inc. (NASDAQ:CRMD) Not Doing Enough For Some Investors As Its Shares Slump 35%The CorMedix Inc. ( NASDAQ:CRMD ) share price has fared very poorly over the last month, falling by a substantial 35...공지 • Feb 03CorMedix Inc. (NasdaqGM:CRMD) announces an Equity Buyback for $75 million worth of its shares.CorMedix Inc. (NasdaqGM:CRMD) announces a share repurchase program. Under the program, the company will repurchase up to $75 million worth of its outstanding common stock. The repurchase program is authorized through December 31, 2027.내러티브 업데이트 • Jan 22CRMD: Updated Revenue Guidance And Investor Day Will Shape Upside PotentialNarrative Update Analysts have trimmed their average price target for CorMedix from about US$19 to roughly US$16.86. This reflects updated expectations for slower revenue growth and lower profit margins, partially offset by a higher assumed future P/E multiple following the company's reduced long term guidance and recent research updates.공지 • Jan 08+ 1 more updateCorMedix Inc. Announces Board and Executive ChangesCorMedix Therapeutics announced that Joseph Todisco in addition to his role as CEO, Mr. Todisco will also assume the role of Chairman of the Board of Directors, succeeding Myron Kaplan. Mr. Kaplan will transition into a newly created board position of Lead Independent Director. CorMedix announced the appointment of Mr. Mike Seckler to the role of EVP & Chief Commercial Officer. Mr. Seckler joins CorMedix with a wealth of experience across multiple therapeutic areas including hematology and oncology, and most recently served as CEO of Evome Medical Technologies Inc. Mr. Seckler’s previous experience includes roles as COO of FerGene Inc., a Blackstone Life Sciences and Ferring Pharmaceuticals joint partnership gene therapy company, as well as head of Global Marketing and Corporate Communications for Ferring International.내러티브 업데이트 • Jan 07CRMD: Robust Q3 Sales And Synergy Progress Will Support Further UpsideNarrative Update: CorMedix Analysts have maintained their fair value estimate for CorMedix at $19.00. Recent Street research highlights a $14.00 price target supported by what they describe as "robust" preliminary Q3 sales, better visibility into near term operating synergies, and the recent stock pullback.분석 기사 • Dec 23CorMedix Inc.'s (NASDAQ:CRMD) 28% Jump Shows Its Popularity With InvestorsCorMedix Inc. ( NASDAQ:CRMD ) shares have had a really impressive month, gaining 28% after a shaky period beforehand...공지 • Dec 18Cormedix Therapeutics Announces Positive Data from Ongoing Real World Evidence Study of DefencathCorMedix Therapeutics announced interim results for the Company's ongoing real-world evidence study being conducted in conjunction with U.S. Renal Care's (USRC) use of DefenCath in adult hemodialysis patients with central venous catheters. CorMedix and USRC commenced the real-world evidence study upon outpatient commercial launch in July 2024. The study is designed to demonstrate the impact of the broad use of DefenCath in a real-world setting and prospectively assess rates of catheter-related bloodstream infections (CRBSI), as well as hospitalizations secondary to these infections. The study is designed to evaluate these data points for two years. Currently, more than 3,000 patients per month are receiving DefenCath on a routine basis at USRC facilities. The company believe this data also strongly reinforces the ongoing collaborations among healthcare providers, patient advocates and elected leaders committed to transforming status quo dialysis care by addressing the long-standing and unmet need for infection prevention measures that lower hospitalizations, reduce healthcare utilization and limit costs to taxpayers. Secondary data points of missed treatment sessions, antibiotic utilization, and tPA utilization are also being assessed and may be announced with additional real-world evidence data in the future. CorMedix believes these data from this large, prospective, ongoing real-world study further underscore the LOCK-IT 100 clinical study results on which the FDA approval of DefenCath for ESRD hemodialysis patients was based. The Company expects to continue to discuss with customers and payors, such as Medicare Advantage plans, to emphasize the economic value of long-term infection prevention in these patients.내러티브 업데이트 • Dec 14CRMD: Robust Q3 Sales Will Support Stronger Upside Momentum AheadAnalysts have modestly raised their price target on CorMedix to $19.00 from $14.00, citing robust preliminary Q3 sales, clearer visibility into near term operating synergies, and the recent stock pullback as key drivers of their more constructive outlook. Analyst Commentary Bullish Takeaways Bullish analysts highlight that robust preliminary Q3 sales provide early validation of CorMedix's commercial strategy and support the raised price target.내러티브 업데이트 • Nov 28CRMD: Q3 Sales Strength And New Buy Rating Will Drive Momentum ForwardAnalysts have raised their price target for CorMedix to $14 from the previous level, citing stronger than expected Q3 sales and improved visibility into operational performance as key drivers of the updated outlook. Analyst Commentary Following the recent preliminary Q3 results, analysts have provided updated insights into CorMedix’s outlook, highlighting both encouraging signs and ongoing areas of caution for the company’s future performance.내러티브 업데이트 • Nov 14CRMD: Strong Q3 Sales Will Drive Renewed Uptrend MomentumAnalysts have lowered their price target for CorMedix from $20.40 to $19.00, citing a more moderate revenue growth outlook and adjusted profit expectations. This comes despite optimism about robust Q3 sales and operational improvements.공지 • Nov 12+ 1 more updateCorMedix Inc. Raises Earnings Guidance for the Year Ending December 31, 2025CorMedix Inc. raised earnings guidance for the year ending December 31, 2025. For the year, the company raises its full-year 2025 pro forma net revenue guidance to a range of $390 to $410 million.공지 • Oct 31CorMedix Inc. to Report Q3, 2025 Results on Nov 12, 2025CorMedix Inc. announced that they will report Q3, 2025 results Pre-Market on Nov 12, 2025공지 • Sep 30CorMedix Announces Completion of Enrollment in Phase III ReSPECT Clinical Trial for REZZAYOCorMedix Inc. announced completion of enrollment for the ongoing, global Phase III ReSPECT trial evaluating the efficacy of REZZAYO®? (rezafungin), a single-agent echinocandin in the prevention of Candida, Aspergillus, and Pneumocystis infection in patients undergoing allogeneic blood and marrow transplantation (BMT). This clinical trial has been sponsored by Mundipharma, located in the United Kingdom. The US distribution rights for REZZAYO were licensed under a strategic collaboration agreement with Melinta Therapeutics, LLC, a wholly owned subsidiary of CorMedix. The ReSPECT clinical trial is a Phase III, multicenter, randomized, double-blind study evaluating the efficacy and safety of once-weekly rezafungin (REZZAYO) versus a standard antimicrobial regimen (SAR) for the prevention of invasive fungal diseases (IFDs) in adults undergoing allogeneic BMT. Participants in the experimental arm receive a 400 mg loading dose of rezafungin in week one, followed by 200 mg weekly for 13 weeks, along with oral placebo matching the SAR components. The primary endpoint is fungal-free survival at day 90, with secondary objectives including incidence of IFD, discontinuation due to toxicity, and mortality adjusted for comorbidities. There are an estimated 50,000 cases of candidemia and invasive candidiasis each year in the U.S.REZZAYO is currently being studied for the prevention of invasive fun Gal diseases in adults undergoing allogeneicBMT. CorMedix estimates that there are an approximately 130,000 patients that could constitute the addressable market for antifungal prophylaxis in the U.S. and estimates an implied total addressable market ("TAM") of over $2B in this market segment. REZZAYO has orphan drug exclusivity through 2035 and patent coverage through 2038 in the U.S.내러티브 업데이트 • Sep 04Acquisition And Pipeline Expansion Will Unlock Healthcare PotentialCorMedix’s consensus price target has edged up to $20.40, as analysts see greater revenue potential from DefenCath’s accelerating launch, expanded patient uptake, and supportive reimbursement dynamics, offsetting equity-related dilution concerns. Analyst Commentary The recent $85M equity offering extends CorMedix's cash runway but introduces dilution, prompting a reduced price target from previous levels based on valuation concerns.공지 • Sep 03+ 2 more updatesCorMedix Inc. Announces Executive Changes, Effective August 29, 2025CorMedix Inc. announced that it has successfully completed its previously announced acquisition of Melinta Therapeutics LLC. The following executives will form the core of the senior leadership team of the newly merged company serving in roles that are the same or essentially similar to the one each executive currently holds, unless otherwise stated: Susan Blum, CFO of Melinta Therapeutics LLC, will assume the role of EVP & Chief Financial Officer; Dr. Matt David, EVP & CFO of CorMedix Inc., will assume the newly created role of EVP & Chief Business Officer; Liz Hurlburt, EVP & Chief Clinical Strategy and Operations Officer of CorMedix Inc., will assume the newly created role of EVP & Chief Operating Officer, and will serve as Chief Integration Officer; Beth Steinbrenner, SVP and Chief Human Resource Officer of CorMedix Inc., will continue in her role for the newly merged company; and Beth Zelnick Kaufman, EVP & Chief Legal and Compliance Officer and Corporate Secretary of CorMedix Inc., will continue in her role for the newly merged company.분석 기사 • Aug 14Statutory Earnings May Not Be The Best Way To Understand CorMedix's (NASDAQ:CRMD) True PositionThe latest earnings release from CorMedix Inc. ( NASDAQ:CRMD ) disappointed investors. Our analysis found several...분석 기사 • Aug 09It's A Story Of Risk Vs Reward With CorMedix Inc. (NASDAQ:CRMD)NasdaqGM:CRMD 1 Year Share Price vs Fair Value Explore CorMedix's Fair Values from the Community and select yours With...공지 • Aug 08CorMedix Inc. (NasdaqGM:CRMD) agreed to acquire an unknown majority stake in Melinta Therapeutics, LLC from Deerfield Management Company, L.P. for approximately $330 million.CorMedix Inc. (NasdaqGM:CRMD) agreed to acquire an unknown majority stake in Melinta Therapeutics, LLC from Deerfield Management Company, L.P. for approximately $330 million on August 7, 2025. A cash consideration of $260 million will be paid by CorMedix Inc. As part of consideration, $325 million is paid towards common equity of Melinta Therapeutics, LLC. The transaction is subject to approval by regulatory board. The transaction is subject to the expiration or termination of the waiting period under the Hart-Scott-Rodino Antitrust Improvements Act of 1976 (the ‘HSR Act’). The Company expects the transaction to close as early as September 1, 2025. The cash consideration will be funded by a combination of the Company’s existing cash on hand and a $150 million Convertible Notes Offering Evercore Inc. acted as financial advisor for Melinta Therapeutics, LLC. Fenwick & West LLP acted as legal advisor for Melinta Therapeutics, LLC. Katten Muchin Rosenman LLP acted as legal advisor for Deerfield Management Company, L.P. Jared Fertman and Andrew Marmer of Willkie Farr & Gallagher LLP acted as legal advisor to CorMedix Inc.공지 • Aug 07CorMedix Inc. Provides Earnings Guidance for the Full Year 2025CorMedix Inc. provided earnings guidance for the full year 2025. For the year, the company expects Pro Forma 2025 Revenue: $305 million – $335 million.공지 • Jun 30+ 5 more updatesCorMedix Inc.(NasdaqGM:CRMD) dropped from Russell Small Cap Comp Value IndexCorMedix Inc.(NasdaqGM:CRMD) dropped from Russell Small Cap Comp Value Index공지 • Jun 27CorMedix Inc. has completed a Follow-on Equity Offering in the amount of $85 million.CorMedix Inc. has completed a Follow-on Equity Offering in the amount of $85 million. Security Name: Common Stock Security Type: Common Stock Securities Offered: 6,604,507 Price\Range: $12.869999분석 기사 • Jun 27Bullish: Analysts Just Made A Meaningful Upgrade To Their CorMedix Inc. (NASDAQ:CRMD) ForecastsCelebrations may be in order for CorMedix Inc. ( NASDAQ:CRMD ) shareholders, with the analysts delivering a significant...공지 • Jun 27CorMedix Inc. has filed a Follow-on Equity Offering in the amount of $85 million.CorMedix Inc. has filed a Follow-on Equity Offering in the amount of $85 million. Security Name: Common Stock Security Type: Common Stock공지 • Jun 24CorMedix Inc. Increases Net Sales Guidance of Second Quarter 2025CorMedix Inc. announced that as a result of this new customer implementation and other positive business developments, CorMedix is increasing its second quarter 2025 net sales guidance from the previously communicated $31 million to a range of $35 million to $40 million.공지 • May 06CorMedix Inc. Revises Sales Guidance for the First Half of 2025CorMedix Inc. revised sales guidance for the first half of 2025. The company expected to be at the high-end of the previously announced first half net sales guidance of $62 million to $70 million, based on latest order trends and inventory tracking with current purchasing customers.새 내러티브 • Apr 30DefenCath Launch Will Boost Inpatient And Dialysis Opportunities Strong revenue growth prospects from DefenCath's successful launch and expansion into new segments like inpatient facilities and partnerships. 공지 • Apr 29CorMedix Inc., Annual General Meeting, Jun 24, 2025CorMedix Inc., Annual General Meeting, Jun 24, 2025.공지 • Apr 08CorMedix Inc. Raises Financial Guidance for First Half of 2025CorMedix Inc. raised financial guidance for first half of 2025. Since providing initial guidance, the Company received larger than expected orders during the final week of March, and has also obtained additional visibility into inventory levels on hand at some of its current purchasing customers. Based on this new information, CorMedix is increasing its first half 2025 guidance for Net Sales to existing purchasing customers to a revised range of $62 million to $70 million.Seeking Alpha • Mar 26The Hidden Risks Behind CorMedix's First Profitable QuarterSummary CorMedix Inc.'s DefenCath reduces catheter infections by 71%, but the limited market potential challenges long-term adoption. Early strong revenues likely reflect inventory building rather than sustained utilization patterns. Special reimbursements boosting current profits will expire, threatening future margins and pricing power. Half-year guidance signals limited visibility, with management warning of inventory adjustments and price erosion. Monte Carlo simulations suggest CRMD faces more downside risk (25%) than upside potential (8.8%). Read the full article on Seeking Alpha공지 • Mar 25CorMedix Inc. Provides Preliminary Earnings Guidance for the First Half of 2025CorMedix Inc. provides preliminary earnings guidance for the first half of 2025. For the year, the company expects net revenue guidance for first half of 2025 of $50– $60 million, based on the run rate of current purchasing customers, with more than $33 million expected in first quarter.공지 • Mar 18CorMedix Inc. to Report Q4, 2024 Results on Mar 25, 2025CorMedix Inc. announced that they will report Q4, 2024 results Pre-Market on Mar 25, 2025분석 기사 • Jan 17Here's Why We're Not Too Worried About CorMedix's (NASDAQ:CRMD) Cash Burn SituationJust because a business does not make any money, does not mean that the stock will go down. Indeed, CorMedix...Seeking Alpha • Jan 07CorMedix: Finally In Commercialization ModeSummary CorMedix Inc.'s DefenCath, an antimicrobial catheter lock solution, shows considerable promise in reducing catheter-related bloodstream infections. The product was approved earlier this year and has seen solid initial sales traction. Analyst firms are optimistic about the company's prospects, even as the stock is down just over a third from recent highs. An analysis of CorMedix follows in the paragraphs below. Read the full article on Seeking Alpha분석 기사 • Dec 13CorMedix Inc.'s (NASDAQ:CRMD) P/S Is On The MarkWhen you see that almost half of the companies in the Pharmaceuticals industry in the United States have price-to-sales...분석 기사 • Nov 14Here's Why CorMedix Inc.'s (NASDAQ:CRMD) CEO Compensation Is The Least Of Shareholders' ConcernsKey Insights CorMedix to hold its Annual General Meeting on 21st of November CEO Joe Todisco's total compensation...분석 기사 • Nov 04Analysts Just Made A Massive Upgrade To Their CorMedix Inc. (NASDAQ:CRMD) ForecastsCelebrations may be in order for CorMedix Inc. ( NASDAQ:CRMD ) shareholders, with the analysts delivering a significant...Seeking Alpha • Oct 28CorMedix 2.0: New Leadership, New Approval, New FocusSummary CorMedix is a biopharmaceutical company that has undergone a re-birth as it enters a new phase with FDA approval of its anti-infective catheter solution, DefenCath. The company has faced challenges in the past, including management issues and regulatory delays, but now warrants a fresh look and valuation as the company executes on commercialization. DefenCath offers a unique solution for preventing catheter-related bloodstream infections, with the potential to reduce costs and save lives. Read the full article on Seeking Alpha공지 • Oct 23CorMedix Inc. to Report Q3, 2024 Results on Oct 30, 2024CorMedix Inc. announced that they will report Q3, 2024 results on Oct 30, 2024Seeking Alpha • Oct 19CorMedix: Delayed Approval, Low Cash, Good ProspectsSummary CorMedix's DefenCath, an FDA-approved antimicrobial catheter lock solution, significantly reduces catheter-related bloodstream infections, addressing a critical need in hemodialysis patients. DefenCath's market exclusivity and reimbursement strategies position it well in the growing $2.6bn CRBSI market, with significant potential for revenue. Despite past challenges, CorMedix's financial outlook is improving, but additional funds are needed for future trials in new indications. Investors should await Q3 earnings data for a clearer picture, as current stock spikes are driven by DefenCath's recent launch. Read the full article on Seeking Alpha공지 • Oct 09CorMedix Inc., Annual General Meeting, Nov 21, 2024CorMedix Inc., Annual General Meeting, Nov 21, 2024.분석 기사 • Sep 30We're Hopeful That CorMedix (NASDAQ:CRMD) Will Use Its Cash WiselyJust because a business does not make any money, does not mean that the stock will go down. For example, CorMedix...공지 • Aug 07CorMedix Inc. to Report Q2, 2024 Results on Aug 14, 2024CorMedix Inc. announced that they will report Q2, 2024 results Pre-Market on Aug 14, 2024공지 • May 11CorMedix Inc. has filed a Follow-on Equity Offering in the amount of $50 million.CorMedix Inc. has filed a Follow-on Equity Offering in the amount of $50 million. Security Name: Common Stock Security Type: Common Stock Transaction Features: At the Market Offering공지 • May 08CorMedix Inc. to Report Q1, 2024 Results on May 09, 2024CorMedix Inc. announced that they will report Q1, 2024 results Pre-Market on May 09, 2024공지 • Apr 15CorMedix Inc. Announces U.S. Inpatient Commercial Availability of DefenCath®? (Taurolidine and Heparin)CorMedix Inc. announced DefenCath®? (taurolidine and heparin) catheter lock solution (CLS) is now commercially available for U.S. inpatient use. DefenCath (taurolidine and Heparin) is approved by the U.S. Food and Drug Administration (FDA) to reduce the incidence of catheter-related bloodstream infections (CRBSIs) in adult patients with kidney failure receiving chronic hemodialysis through a central venous catheter (HD-CVC). The commencement of U.S. outpatient commercialization of DefenCath is planned for July 1, 2024. Outpatient commercial availability is contingent upon the Center for Medicare & Medicaid Services (CMS) approval and implementation of the DefenCath Transitional Drug Add-On Payment Adjustment (TDAPA) application in accordance with the agency's publicly stated objective that CMS aims for an effective date for applying the TDAPA for a particular product that is one quarter after the effective date of the HCPCS code for the product. The CMS Final HCPCS coding decision for DefenCath was published by CMS on April 2nd, establishing a new HCPCS Level II code for DefenCath, and CorMedix continues to work closely with CMS on the TDAPA implementation process.New Risk • Apr 11New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of American stocks, typically moving 10% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Major Risk Revenue is less than US$1m. Minor Risks Share price has been volatile over the past 3 months (10% average weekly change). Shareholders have been diluted in the past year (24% increase in shares outstanding).분석 기사 • Apr 06We Think CorMedix (NASDAQ:CRMD) Can Afford To Drive Business GrowthEven when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...Recent Insider Transactions • Mar 15CEO & Director recently bought US$51k worth of stockOn the 13th of March, Joseph Todisco bought around 14k shares on-market at roughly US$3.74 per share. This transaction amounted to 10% of their direct individual holding at the time of the trade. This was the largest purchase by an insider in the last 3 months. Joseph has been a buyer over the last 12 months, purchasing a net total of US$111k worth in shares.Breakeven Date Change • Mar 13Forecast breakeven date moved forward to 2025The 4 analysts covering CorMedix previously expected the company to break even in 2026. New consensus forecast suggests losses will reduce by 2.8% to 2024. The company is expected to make a profit of US$6.71m in 2025. Average annual earnings growth of 60% is required to achieve expected profit on schedule.공지 • Mar 07CorMedix Inc. to Report Q4, 2023 Results on Mar 12, 2024CorMedix Inc. announced that they will report Q4, 2023 results Pre-Market on Mar 12, 2024Price Target Changed • Feb 01Price target decreased by 7.0% to US$13.25Down from US$14.25, the current price target is an average from 4 analysts. New target price is 349% above last closing price of US$2.95. Stock is down 34% over the past year. The company is forecast to post a net loss per share of US$0.85 next year compared to a net loss per share of US$0.74 last year.공지 • Jan 31CorMedix Inc. Updates Related to Its Business and Anticipated Launch of DefenCathCorMedix Inc. announced updates related to its business and anticipated launch of DefenCath. On January 25, 2024 the Center for Medicare & Medicaid Services (CMS) notified CorMedix that the agency has determined DefenCath will be eligible for reimbursement in accordance with the ESRD PPS. As such, CorMedix is entitled to submit an application for a Transitional Drug Add-On Payment (TDAPA) which currently allows for five years of additional payment reimbursement to outpatient providers. CorMedix submitted its TDAPA application on January 26 after receiving the CMS notification, and CMS has subsequently confirmed receipt. As a result of CMS' determination that DefenCath is within the scope of the ESRD PPS and eligible for TDAPA, CorMedix has established its list price (WAC) of $249.99 per 3ml vial, to account for the market dynamics and functionality of the TDAPA framework. Should CMS make a future determination that DefenCath is eligible for Medicare Part B reimbursement, CorMedix has committed to CMS to reduce the list price accordingly. CorMedix previously applied for and received a New Technology Add-On Payment (NTAP) from CMS for inpatient reimbursement of DefenCath. Now that the company has established a WAC price for commercialization, CorMedix will notify CMS accordingly to make any necessary adjustment to the NTAP reimbursement payment to inpatient facilities.공지 • Jan 08Cormedix Inc. Announces Commercial and Operational UpdatesCorMedix Inc. announced several commercial and operational updates related to its business and anticipated launch of DefenCath®. Recent Updates: CorMedix formally submitted an HCPCS application for a J-Code to the Center for Medicare and Medicaid Services (CMS) on December 8, 2023 for DefenCath, and CMS has confirmed the application is under review. The Company continues to engage in discussions with CMS related to the appropriate outpatient reimbursement structure for DefenCath and remains committed to its pursuit of separate payment under Medicare Part B as the appropriate reimbursement mechanism for the product. In such an instance, the Company expects to establish a list price based on the market dynamics for both inpatient contracting as well as a Transitional Drug Add-On Payment (TDAPA) framework for outpatient reimbursement. CorMedix would then subsequently revise the list price downward should CMS make a determination in favor of separate payment under Medicare PartB. CorMedix expects to provide further detail on the DefenCath market opportunity as the company receive clarity from CMS regarding outpatient reimbursement. The Company believes it has sufficient cash, cash equivalents and available resources to fund the commercial launch.Breakeven Date Change • Dec 31Forecast to breakeven in 2026The 4 analysts covering CorMedix expect the company to break even for the first time. New consensus forecast suggests the company will make a profit of US$16.6m in 2026. Average annual earnings growth of 59% is required to achieve expected profit on schedule.공지 • Dec 16CorMedix Inc. Approves the Separation of Employment of Phoebe MountsOn December 12, 2023, upon mutual agreement between CorMedix Inc. (the “Company”) and Phoebe Mounts, Ph.D., Esq., the Company’s Executive Vice President, General Counsel and Corporate Secretary, the Board of Directors of the Company (the “Board”) approved the separation of employment of Dr. Mounts, effective December 31, 2023 (the “Termination Date”). Dr. Mounts will cease to hold the title of General Counsel and Corporate Secretary effective December 12, 2023. Until the Termination Date, Dr. Mounts will continue to serve as Executive Vice President and devote her time and attention to facilitating the transition of her duties and responsibilities.공지 • Dec 15CorMedix Inc. Announces the Appointment of Beth Zelnick Kaufman, Esq. as Executive Vice President, Chief Legal Officer, and Corporate Secretary, Effective December 12, 2023CorMedix Inc. announced the appointment of Beth Zelnick Kaufman, Esq. as EVP, Chief Legal Officer, and Corporate Secretary, effective December 12, 2023. The Company also announced that, upon mutual agreement with the Company, Dr. Phoebe Mounts will no longer serve as the Company’s General Counsel, effective December 12, 2023, and will be separating from CorMedix effective December 31, 2023, to pursue other opportunities. Ms. Zelnick Kaufman has more than two decades of legal, compliance and operations experience in the life sciences industry. Prior to joining CorMedix, she most recently served as Chief Legal and Administrative Officer and Corporate Secretary of Akorn Pharmaceuticals, a specialty and generic pharmaceuticals company. Ms. Zelnick Kaufman also served in several roles at Amneal Pharmaceuticals, a publicly traded global generics, biosimilars and branded pharmaceuticals company, including roles as Assistant General Counsel, Vice President, Legal Affairs, and Head of Government Affairs. During her tenure at these and other pharmaceutical companies, Ms. Zelnick Kaufman gained deep experience in the pharmaceutical industry across legal, regulatory, government affairs, and other operational areas. Earlier in her career, Ms. Zelnick Kaufman held roles at Actavis, Alpharma and Topcon America and spent time as an Associate in the law firm Brown, Rudnick. Ms. Zelnick Kaufman holds a Juris Doctor degree from New York University Law School and a Bachelor of Arts degree from Amherst College.공지 • Nov 17CorMedix Inc. Announces FDA Approval of DefenCath(R) to Reduce the Incidence of Catheter Related Bloodstream Infections in Adult Hemodialysis PatientsCorMedix Inc. announced that the U.S. Food and Drug Administration (FDA) has approved DefenCath(R) (taurolidine and heparin) catheter lock solution (CLS) to reduce the incidence of catheter-related bloodstream infections (CRBSIs) for the limited population of adult patients with kidney failure receiving chronic hemodialysis through a central venous catheter (CVC). DefenCath is the first and only FDA-approved antimicrobial CLS in the U.S. and was shown to reduce the risk of CRBSIs by up to 71% in a Phase 3 clinical study. The FDA approval of DefenCath was supported by results from the randomized, double-blind, active control, multicenter pivotal Phase 3 LOCK-IT-100 clinical trial designed to assess the efficacy and safety of DefenCath for reducing the incidence of CRBSIs in patients with kidney failure receiving chronic Hemodialysis through a central Venous catheter. The FDA approval of DefENCath was supported by results from The randomized, double-blind, Active control, multicenter pivotal Phase3 LOCK-IT-100clinical trial designed to assess the efficacy, safety of DefenCath for reduce the incidence of CRBSIs In the study, a total of 806 subjects were randomized to receive either DefenCath or heparin as a CLS. Until now, patients who need hemodialysis via a central venous catheter have had little choice other than to accept high infection risks associated with the existing standard of care. The FDA's approval of DefenCath is a meaningful moment for patients and their healthcare providers because they now have a new alternative to reduce the risks of CRBSIs. DefenCath is an antimicrobial catheter lock solution (CL S) approved by the FDA to reduce the incidence of cat catheter-related bloodstream infections ("CRBSIs") for the limited population of adult patient with kidney failure receiving chronic he modialysis through a central venal catheter (CVC). In addition, FDA designated DefenCath as a Qualified Infectious Disease Product (QIDP) established by the Generating Antibiotic Incentives Now (GAIN) Act that supports development of antibacterial and antifungal products that treat serious or life-threatening infections. DefenCath has been designated by FDA as Fast-up, and FDA as Fast-up, a novel, non-antibiotic antimicrobial antimicrobial solution designed to prevent costly and life-threatening bloodstream infections associated with the use of central venous catheters in patients undergoing chronic hemodialysis. DefenCath has been identified by FDA as Fast-up and FDA as Fast-up and a Phase 3 clinical study.Reported Earnings • Nov 16Third quarter 2023 earnings released: US$0.17 loss per share (vs US$0.17 loss in 3Q 2022)Third quarter 2023 results: US$0.17 loss per share (further deteriorated from US$0.17 loss in 3Q 2022). Net loss: US$9.74m (loss widened 42% from 3Q 2022). Revenue is forecast to grow 58% p.a. on average during the next 3 years, compared to a 8.4% growth forecast for the Pharmaceuticals industry in the US. Over the last 3 years on average, earnings per share has fallen by 3% per year but the company’s share price has fallen by 20% per year, which means it is performing significantly worse than earnings.공지 • Nov 03CorMedix Inc. to Report Q3, 2023 Results on Nov 14, 2023CorMedix Inc. announced that they will report Q3, 2023 results After-Market on Nov 14, 2023분석 기사 • Nov 02We're Hopeful That CorMedix (NASDAQ:CRMD) Will Use Its Cash WiselyEven when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...공지 • Sep 14CorMedix Inc., Annual General Meeting, Oct 26, 2023CorMedix Inc., Annual General Meeting, Oct 26, 2023, at 09:00 US Eastern Standard Time. Agenda: To elect seven directors to serve until the 2024 Annual Meeting of Stockholders and until their successors are duly elected and qualified; to approve on a non-binding advisory basis the compensation of company's named executive officers for 2022; to ratify the appointment of Marcum LLP as company's independent registered public accounting firm for the fiscal year ending December 31, 2023; and to act upon such other matters as may properly come before the meeting or any adjournment, postponement or continuation thereof.공지 • Aug 18Cormedix Inc. Announces Resignation of Paulo F. Costa as Member of the Board of Directors, Effective as of October 15, 2023CorMedix Inc. announced that Paulo F. Costa, a member of the Board of Directors notified the Board that he will be retiring from the Board, effective as of October 15, 2023. The Company does not intend to fill Mr. Costa’s seat on the Board at this time and therefore the size of the Board will be reduced to seven directors effective as of October 15, 2023. The Company expressed gratitude to Mr. Costa for his contributions to the Board and the Company. Mr. Costa’s departure is not as a result of any dispute or disagreement with the Company, its management, the Board, or any matter relating to the Company’s operations, policies or practices. The Board is evaluating how it intends to fill Mr. Costa’s committee assignment.Price Target Changed • Aug 11Price target decreased by 18% to US$13.75Down from US$16.67, the current price target is an average from 4 analysts. New target price is 212% above last closing price of US$4.40. Stock is up 6.0% over the past year. The company is forecast to post a net loss per share of US$1.02 next year compared to a net loss per share of US$0.74 last year.Reported Earnings • Aug 08First half 2023 earnings released: US$0.49 loss per share (vs US$0.38 loss in 1H 2022)First half 2023 results: US$0.49 loss per share (further deteriorated from US$0.38 loss in 1H 2022). Net loss: US$21.8m (loss widened 49% from 1H 2022). Revenue is forecast to grow 61% p.a. on average during the next 3 years, compared to a 7.1% growth forecast for the Pharmaceuticals industry in the US. Over the last 3 years on average, earnings per share has increased by 15% per year but the company’s share price has only increased by 3% per year, which means it is significantly lagging earnings growth.분석 기사 • Jul 31Here's Why We're Not Too Worried About CorMedix's (NASDAQ:CRMD) Cash Burn SituationEven when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...공지 • Jul 28CorMedix Inc. to Report Q2, 2023 Results on Aug 08, 2023CorMedix Inc. announced that they will report Q2, 2023 results Pre-Market on Aug 08, 2023공지 • Jun 22CorMedix Inc. Announces FDA Acceptance of Resubmission of New Drug Application for DefenCathCorMedix Inc. announced that the resubmission of the New Drug Application (NDA) for DefenCath has been accepted for filing by the U.S. Food and Drug Administration (FDA). The Agency considers the resubmission as a complete, Class 2 response with a six-month review, and has assigned a Prescription Drug User Fee Act (PDUFA) target action date of November 15, 2023. DefenCath is being developed as a catheter lock solution with an initial indication of use for the reduction of catheter-related bloodstream infections (CRBSIs) in patients with kidney failure who are receiving chronic hemodialysis via a central venous catheter.공지 • May 17Cormedix Inc. Announces Resubmission of New Drug Application for DefencathCorMedix Inc. announced that the New Drug Application for DefenCath was resubmitted to the U.S. Food and Drug Administration, and the submission has been acknowledged as received for processing.Reported Earnings • May 17First quarter 2023 earnings released: US$0.24 loss per share (vs US$0.18 loss in 1Q 2022)First quarter 2023 results: US$0.24 loss per share (further deteriorated from US$0.18 loss in 1Q 2022). Net loss: US$10.6m (loss widened 50% from 1Q 2022). Revenue is forecast to grow 199% p.a. on average during the next 2 years, compared to a 7.1% growth forecast for the Pharmaceuticals industry in the US. Over the last 3 years on average, earnings per share has increased by 27% per year but the company’s share price has only increased by 3% per year, which means it is significantly lagging earnings growth.공지 • May 09CorMedix Inc. to Report Q1, 2023 Results on May 15, 2023CorMedix Inc. announced that they will report Q1, 2023 results at 4:00 PM, US Eastern Standard Time on May 15, 2023Reported Earnings • Mar 31Full year 2022 earnings: Revenues exceed analysts expectations while EPS lags behindFull year 2022 results: US$0.74 loss per share. Net loss: US$29.7m (loss widened 5.3% from FY 2021). Revenue exceeded analyst estimates. Earnings per share (EPS) missed analyst estimates by 1.4%. Revenue is forecast to grow 56% p.a. on average during the next 3 years, compared to a 5.1% growth forecast for the Pharmaceuticals industry in the US.분석 기사 • Feb 25CorMedix (NASDAQ:CRMD) Is In A Good Position To Deliver On Growth PlansJust because a business does not make any money, does not mean that the stock will go down. For example, although...공지 • Jan 18Cormedix Inc. Announces Promotions in Commercial and Tech OpsCorMedix Inc. announced the following promotions within the organization: Erin Miststry, SVP Commercial, has been promoted to EVP and Chief Commercial Officer. Ms. Mistry will have oversight and responsibility for all commercial launch strategy for DefenCath and the build out of launch infrastructure, including but not limited to market access, commercial operations and field-based sales personnel. Ms. Mistry joined CorMedix 2020 and has been an integral architect of the company's go to market and reimbursement strategy. Dr. Tushar Mukherjee, VP of Technical Operations has been promoted to SVP, Head of Technical Operations. Dr. Mukherjee joined CorMedix in early 2022 and has been a valuable leader and contributor for the technical team. In his new role, Dr. Mukherjee will report directly to the CEO and will assume responsibility for the final validation of all manufacturing, packaging and analytical testing of DefenCath, as well as all technical reviews of new product opportunities. Dr. Phoebe Mounts who had previously assumed interim oversight of technical operations will remain with the organization in her critical role as General Counsel and Head of Regulatory Affairs.Recent Insider Transactions • Nov 18CEO & Director recently bought US$76k worth of stockOn the 15th of November, Joseph Todisco bought around 20k shares on-market at roughly US$3.82 per share. This transaction increased Joseph's direct individual holding by 1x at the time of the trade. This was the largest purchase by an insider in the last 3 months. Joseph has been a buyer over the last 12 months, purchasing a net total of US$129k worth in shares.Price Target Changed • Nov 16Price target increased to US$15.00Up from US$14.00, the current price target is an average from 3 analysts. New target price is 307% above last closing price of US$3.69. Stock is down 29% over the past year. The company is forecast to post a net loss per share of US$0.73 next year compared to a net loss per share of US$0.75 last year.Reported Earnings • Nov 16Third quarter 2022 earnings released: US$0.17 loss per share (vs US$0.23 loss in 3Q 2021)Third quarter 2022 results: US$0.17 loss per share (improved from US$0.23 loss in 3Q 2021). Net loss: US$6.85m (loss narrowed 20% from 3Q 2021). Revenue is forecast to grow 79% p.a. on average during the next 3 years, compared to a 3.8% growth forecast for the Pharmaceuticals industry in the US. Over the last 3 years on average, earnings per share has increased by 36% per year but the company’s share price has fallen by 18% per year, which means it is significantly lagging earnings.이익 및 매출 성장 예측NasdaqGM:CRMD - 애널리스트 향후 추정치 및 과거 재무 데이터 (USD Millions)날짜매출이익자유현금흐름영업현금흐름평균 애널리스트 수12/31/2028353688681512/31/2027282307883712/31/202630852101106712/31/2025312162173175N/A9/30/20252141627475N/A6/30/2025121513030N/A3/31/20258317-14-14N/A12/31/202443-18-51-51N/A9/30/202412-46-56-56N/A6/30/20241-53-51-51N/A3/31/2024N/A-50-46-45N/A12/31/2023N/A-46-39-38N/A9/30/20230-40-34-34N/A6/30/20230-37-31-31N/A3/31/20230-33-28-28N/A12/31/20220-30-25-24N/A9/30/20220-29-25-24N/A6/30/20220-31-25-24N/A3/31/20220-28-23-21N/A12/31/20210-28-23-21N/A9/30/20210-27-22-21N/A6/30/20210-25-23-23N/A3/31/20210-24-21-21N/A12/31/20200-22-22-22N/A9/30/20200-21-20-20N/A6/30/20200-47-17-17N/A3/31/20200-44-16-16N/A12/31/20190-44-15-15N/A9/30/20190-36N/A-18N/A6/30/20191-14N/A-20N/A3/31/20191-22N/A-24N/A12/31/20180-27N/A-24N/A9/30/20180-39N/A-24N/A6/30/20180-39N/A-25N/A3/31/20180-36N/A-29N/A12/31/20170-33N/A-29N/A9/30/20170-29N/A-28N/A6/30/20170-28N/A-28N/A3/31/20170-28N/A-24N/A12/31/20160-25N/A-22N/A9/30/20160-22N/A-19N/A6/30/20160-18N/A-16N/A3/31/20160-17N/A-16N/A12/31/20150-18N/A-13N/A9/30/20150-17N/A-10N/A6/30/20150-17N/A-9N/A더 보기애널리스트 향후 성장 전망수입 대 저축률: CRMD 의 연간 예상 수익 증가율(8.4%)이 saving rate(3.5%)보다 높습니다.수익 vs 시장: CRMD 의 연간 수익(8.4%)이 US 시장(16.7%)보다 느리게 성장할 것으로 예상됩니다.고성장 수익: CRMD 의 수입은 증가할 것으로 예상되지만 상당히 증가하지는 않을 것입니다.수익 대 시장: CRMD 의 수익(연간 12.4%)이 US 시장(연간 11.6%)보다 빠르게 성장할 것으로 예상됩니다.고성장 매출: CRMD 의 수익(연간 12.4%)은 연간 20%보다 느리게 증가할 것으로 예상됩니다.주당순이익 성장 예측향후 자기자본이익률미래 ROE: CRMD의 자본 수익률이 3년 후 높을 것으로 예상되는지 판단하기에 데이터가 부족합니다.성장 기업 찾아보기7D1Y7D1Y7D1YPharmaceuticals-biotech 산업의 고성장 기업.View Past Performance기업 분석 및 재무 데이터 상태데이터최종 업데이트 (UTC 시간)기업 분석2026/05/11 07:45종가2026/05/11 00:00수익2025/12/31연간 수익2025/12/31데이터 소스당사의 기업 분석에 사용되는 데이터는 S&P Global Market Intelligence LLC에서 제공됩니다. 아래 데이터는 이 보고서를 생성하기 위해 분석 모델에서 사용됩니다. 데이터는 정규화되므로 소스가 제공된 후 지연이 발생할 수 있습니다.패키지데이터기간미국 소스 예시 *기업 재무제표10년손익계산서현금흐름표대차대조표SEC 양식 10-KSEC 양식 10-Q분석가 컨센서스 추정치+3년재무 예측분석가 목표주가분석가 리서치 보고서Blue Matrix시장 가격30년주가배당, 분할 및 기타 조치ICE 시장 데이터SEC 양식 S-1지분 구조10년주요 주주내부자 거래SEC 양식 4SEC 양식 13D경영진10년리더십 팀이사회SEC 양식 10-KSEC 양식 DEF 14A주요 개발10년회사 공시SEC 양식 8-K* 미국 증권에 대한 예시이며, 비(非)미국 증권에는 해당 국가의 규제 서식 및 자료원을 사용합니다.별도로 명시되지 않는 한 모든 재무 데이터는 연간 기간을 기준으로 하지만 분기별로 업데이트됩니다. 이를 TTM(최근 12개월) 또는 LTM(지난 12개월) 데이터라고 합니다. 자세히 알아보기.분석 모델 및 스노우플레이크이 보고서를 생성하는 데 사용된 분석 모델에 대한 자세한 내용은 당사의 Github 페이지에서 확인하실 수 있습니다. 또한 보고서 활용 방법에 대한 가이드와 YouTube 튜토리얼도 제공합니다.Simply Wall St 분석 모델을 설계하고 구축한 세계적 수준의 팀에 대해 알아보세요.산업 및 섹터 지표산업 및 섹터 지표는 Simply Wall St가 6시간마다 계산하며, 프로세스에 대한 자세한 내용은 Github에서 확인할 수 있습니다.분석가 소스CorMedix Inc.는 18명의 분석가가 다루고 있습니다. 이 중 7명의 분석가가 우리 보고서에 입력 데이터로 사용되는 매출 또는 수익 추정치를 제출했습니다. 분석가의 제출 자료는 하루 종일 업데이트됩니다.분석가기관Andrew D'SilvaB. Riley Securities, Inc.Jason ButlerCitizens JMP Securities, LLCJason KolbertD. Boral Capital LLC.15명의 분석가 더 보기
공지 • Mar 05CorMedix Inc. Reiterates Earnings Guidance for the Year 2026CorMedix reiterated earnings guidance for the year 2026. For the year, company reiterated previously established guidance for 2026, including net revenue of between $300 and $320 million .
공지 • Nov 12+ 1 more updateCorMedix Inc. Raises Earnings Guidance for the Year Ending December 31, 2025CorMedix Inc. raised earnings guidance for the year ending December 31, 2025. For the year, the company raises its full-year 2025 pro forma net revenue guidance to a range of $390 to $410 million.
공지 • Aug 07CorMedix Inc. Provides Earnings Guidance for the Full Year 2025CorMedix Inc. provided earnings guidance for the full year 2025. For the year, the company expects Pro Forma 2025 Revenue: $305 million – $335 million.
공지 • Jun 24CorMedix Inc. Increases Net Sales Guidance of Second Quarter 2025CorMedix Inc. announced that as a result of this new customer implementation and other positive business developments, CorMedix is increasing its second quarter 2025 net sales guidance from the previously communicated $31 million to a range of $35 million to $40 million.
공지 • May 06CorMedix Inc. Revises Sales Guidance for the First Half of 2025CorMedix Inc. revised sales guidance for the first half of 2025. The company expected to be at the high-end of the previously announced first half net sales guidance of $62 million to $70 million, based on latest order trends and inventory tracking with current purchasing customers.
공지 • Apr 08CorMedix Inc. Raises Financial Guidance for First Half of 2025CorMedix Inc. raised financial guidance for first half of 2025. Since providing initial guidance, the Company received larger than expected orders during the final week of March, and has also obtained additional visibility into inventory levels on hand at some of its current purchasing customers. Based on this new information, CorMedix is increasing its first half 2025 guidance for Net Sales to existing purchasing customers to a revised range of $62 million to $70 million.
내러티브 업데이트 • May 11CRMD: Mixed Research And Phase III Success Will Support Undervalued SharesCorMedix's analyst price target has changed to $15.00 from $14.57 as analysts update their models for revenue growth, profit margins, discount rate and future P/E assumptions following mixed recent Street research. Analyst Commentary Recent research on CorMedix reflects a mix of optimism and caution as analysts adjust their valuation frameworks and expectations for execution.
공지 • May 05CorMedix Inc. to Report Q1, 2026 Results on May 14, 2026CorMedix Inc. announced that they will report Q1, 2026 results Pre-Market on May 14, 2026
내러티브 업데이트 • Apr 30CRMD is trading at 5.9x trough-year EBITDA with the market ascribing near-zero value to two near-term pipeline eventsWith ReSPECT Phase III positive this week, CRMD has resolved its single largest binary risk and now trades at a 63% discount to base case intrinsic value with a bear case floor only 8% below current price, as the REZZAYO prophylaxis sNDA path, DefenCath TPN pipeline, and post-TDAPA revenue recovery converge toward a 2027 inflection that the $7 stock price is not remotely reflecting.
공지 • Apr 29Cormedix Therapeutics Announces Positive Topline Results from Phase III Respect Trial Assessing Rezzayo for the Prophylaxis of Invasive Fungal Diseases in Allogeneic Hematopoietic Stem Cell Transplantation PatientsCorMedix Therapeutics announced positive Phase III topline results from the global ReSPECT clinical trial evaluating REZZAYO (rezafungin for injection) for prophylaxis of invasive fungal diseases (IFDs) in adult patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT). The ReSPECT Phase III study, one of the largest anti-fungal multicenter, randomized, double-blind studies evaluated the efficacy and safety of once weekly rezafungin (rezafungin acetate) compared with a standard antimicrobial regimen (SAR) for the prophylaxis of invasive fungal diseases, including infections caused by Candida, Aspergillus, and Pneumocystis, in adults undergoing allogeneic HSCT. Patients undergoing allogeneic blood and marrow transplantation face prolonged periods of immunosuppression and routinely require extended antifungal prophylaxis, representing a setting where differentiated dosing, improved side effect profile, and reduced DDI is beneficial, and comparable efficacy is expected. The ReSPECT study met its primary endpoint for FDA and EMA for fungal-free survival at Day 90 showing non-inferiority vs. SAR, with 60.7% fungal-free survival at Day 90 for rezafungin compared to 59.0% for standard antimicrobial regimen. This demonstrates that rezafungin’s differentiated pharmacokinetics/pharmacodynamics (PK/PD) profile was comparable to the standard antimicrobial regimen (SAR) in reducing the incidence of invasive fungal infections in a high-risk patient population. Rezafungin was well tolerated, with a safety profile showing a favorable benefit/risk profile for immunocompromised patients. The Phase III study topline results demonstrated comparable efficacy against invasive infections from candida, aspergillus and pneumocystis in both therapeutic arms, as well as comparable mortality. In addition, results showed a favorable profile in multiple secondary endpoints, most notably treatment emergent adverse events leading to dose reduction, interruption or withdrawal of study drug, and treatment emergent adverse events leading to study discontinuation. This clinical trial has been sponsored by Mundipharma. Mundipharma has commercial rights to rezafungin outside the U.S. Mundipharma has partnered with Melinta Therapeutics, LLC, a wholly owned subsidiary of CorMedix for US distribution of rezafungin. The companies anticipate a pre-NDA submission meeting with FDA in the coming months, followed by a target submission of a supplemental New Drug Application (sNDA) to the FDA in Second Half 2026 based on the ReSPECT results. Rezafungin is a next generation echinocandin approved for the treatment of candidemia and invasive candidiasis in adults. Invasive candidiasis continues to be an area of significant unmet need, especially for critically ill patients in hospitals and patients with compromised immune systems. Despite a number of available treatments, the mortality rate for patients with invasive candidiasis is as high as 40%. Rezafungin has been studied for the prophylaxis of invasive fungal diseases in adults undergoing allogeneic HSCT. CorMedix estimates that the potential US market opportunity for REZZAYO in prophylaxis exceeds $2 billion, based on internal analyses and assumptions. These estimates are forward-looking statements and are subject to regulatory approvals, clinical practice considerations, and market adoption. Rezafungin has orphan drug exclusivity through 2035 and patent coverage through 2038 in the U.S. REZZAYO is a Registered Trademark of Mundipharma, used under license by Melinta Therapeutics LLC, a wholly owned subsidiary of CorMedix in the US.
내러티브 업데이트 • Apr 23CRMD: Reaffirmed 2026 Outlook And Buyback Plan Will Support Undervalued SharesAnalysts have trimmed their 12 month price target on CorMedix to $13 from $15, reflecting updated views on revenue growth, profitability, and appropriate future P/E levels for the stock. Analyst Commentary Recent price target revisions to US$13 from US$15 sit alongside continued positive ratings, which gives a mixed message for investors.
공지 • Apr 21CorMedix Inc., Annual General Meeting, Jun 23, 2026CorMedix Inc., Annual General Meeting, Jun 23, 2026.
내러티브 업데이트 • Apr 06CRMD: Investor Day Will Reframe Lower Guidance And Support Undervalued OutlookNarrative Update on CorMedix Analysts have reduced their blended price targets on CorMedix by several dollars to a range of roughly $13 to $16, citing updated company revenue guidance that is materially below prior Street expectations, especially for DefenCath in 2026 and 2027. Analyst Commentary Street research on CorMedix has shifted toward lower valuation targets after the company issued revenue guidance for 2026 and 2027 that sits well below prior expectations, particularly for DefenCath.
Seeking Alpha • Apr 02CorMedix: Waiting On Phase III ReSPECT For A Further Re-Rating (Upgrade)Summary CorMedix Inc. is upgraded to Hold, with near-term upside tied to the pivotal Phase III ReSPECT trial for Rezzayo in Q2 '26. CRMD's FY25 saw strong profitability: $163.1M net income, $401.3M pro forma revenue, and $77.2M adjusted EBITDA, aided by the Melinta acquisition. CRMD stock trades at discounted multiples (8.43x P/E, 4.38x EV/EBITDA), reflecting execution risk and conservative growth assumptions despite robust cash flow. The ReSPECT trial could unlock a $2B prophylaxis market and drive a CRMD stock valuation re-rating if results are positive. Read the full article on Seeking Alpha
새 내러티브 • Apr 02CRMD is trading at 5.9x trough-year EBITDA with the market ascribing near-zero value to two near-term pipeline eventsInvestment Thesis DefenCath's regulatory moat (only FDA-approved antimicrobial CLS in the U.S., NCE+GAIN exclusivity through 2033, composition patent to 2042) is intact and the 72% real-world CRBSI reduction is standard-of-care quality data; the TDAPA pricing step-down is a commercial mechanics event, not a competitive displacement event The stock at $7.02 prices in approximately the bear case ($6.54), meaning investors are effectively receiving the REZZAYO prophylaxis Phase III binary and the DefenCath TPN pipeline for free — an unusual asymmetry for a cash-flow-positive commercial pharma company Operating cash flow of $175M in FY2025 and $148.5M in cash provides full self-funding of pipeline without dilution risk, and the $75M buyback at current prices represents management's explicit capital allocation conviction about intrinsic value The Melinta acquisition was well-priced ($30M goodwill on $391M identified intangibles) and adds an annualizing $130M+ revenue stream with shared call points that provide SG&A leverage as the combined platform scales Post-TDAPA recovery in 2027 (3x–5x higher add-on payment vs. H2 2026 per management, plus Medicare Advantage contracting upside not in guidance) provides a clearly identified catalyst path back to re-rating independent of pipeline success Risk Considerations ReSPECT Phase III failure (data Q2 2026) would eliminate ~$221M of base case rNPV, trigger impairment of the $143M IPR&D intangible, and likely reset the stock to the $5.60 52-week low or below — this is the primary binary risk and is near-term Customer concentration at 79% revenue from three accounts is structurally dangerous; any publicly announced reduction in DefenCath orders from a major dialysis organization would be a material negative event with little warning The Q4 GAAP EPS miss ($0.16 vs.
내러티브 업데이트 • Mar 22CRMD: Investor Day Will Clarify Lower Guidance And Highlight Perceived UpsideAnalysts have trimmed CorMedix price targets by $2 to $9, with recent cuts such as $20 to $16 and $15 to $13, reflecting updated views on DefenCath revenue guidance and the company outlook shared in recent research notes. Analyst Commentary Recent research reflects a reset in expectations for CorMedix as analysts align their models with the latest DefenCath revenue guidance and management commentary.
내러티브 업데이트 • Mar 08CRMD: Investor Day Reset On Lower Guidance Will Highlight Undervalued UpsideNarrative Update on CorMedix The analyst price target for CorMedix has been trimmed from about $14.86 to roughly $14.57. Analysts are recalibrating their models in light of lower revenue growth and margin expectations, along with a more conservative view on long term DefenCath contribution, as reflected in recent target cuts from $20 to $16, $15 to $13, and other reductions across the Street.
공지 • Mar 05CorMedix Inc. Reiterates Earnings Guidance for the Year 2026CorMedix reiterated earnings guidance for the year 2026. For the year, company reiterated previously established guidance for 2026, including net revenue of between $300 and $320 million .
공지 • Mar 02CorMedix Inc. to Report Q4, 2025 Results on Mar 05, 2026CorMedix Inc. announced that they will report Q4, 2025 results Pre-Market on Mar 05, 2026
내러티브 업데이트 • Feb 21CRMD: Investor Day Will Reframe Lower Guidance And Support Undervalued ThesisAnalysts have trimmed their average price targets on CorMedix by a mid single digit dollar amount, citing the company's new FY26 and 2027 DefenCath revenue guidance, which sits well below prior Street expectations, as a key driver of their revised views. Analyst Commentary Bullish Takeaways Bullish analysts still see room for upside even with price targets trimmed, suggesting they view the lower guidance as already influencing valuation assumptions.
내러티브 업데이트 • Feb 07CRMD: Investor Day And New Revenue Guidance Will Shape Bullish CaseAnalysts have trimmed their price targets on CorMedix, with our fair value estimate moving from US$16.86 to US$14.86 as they factor in lower revenue growth and profit margin assumptions, despite a higher future P/E multiple. Analyst Commentary Bullish Takeaways Bullish analysts still see upside potential in CorMedix shares, pointing to the higher future P/E multiple being used in their models as a sign that they are willing to ascribe a premium to the company despite reduced revenue assumptions.
분석 기사 • Feb 06CorMedix Inc. (NASDAQ:CRMD) Not Doing Enough For Some Investors As Its Shares Slump 35%The CorMedix Inc. ( NASDAQ:CRMD ) share price has fared very poorly over the last month, falling by a substantial 35...
공지 • Feb 03CorMedix Inc. (NasdaqGM:CRMD) announces an Equity Buyback for $75 million worth of its shares.CorMedix Inc. (NasdaqGM:CRMD) announces a share repurchase program. Under the program, the company will repurchase up to $75 million worth of its outstanding common stock. The repurchase program is authorized through December 31, 2027.
내러티브 업데이트 • Jan 22CRMD: Updated Revenue Guidance And Investor Day Will Shape Upside PotentialNarrative Update Analysts have trimmed their average price target for CorMedix from about US$19 to roughly US$16.86. This reflects updated expectations for slower revenue growth and lower profit margins, partially offset by a higher assumed future P/E multiple following the company's reduced long term guidance and recent research updates.
공지 • Jan 08+ 1 more updateCorMedix Inc. Announces Board and Executive ChangesCorMedix Therapeutics announced that Joseph Todisco in addition to his role as CEO, Mr. Todisco will also assume the role of Chairman of the Board of Directors, succeeding Myron Kaplan. Mr. Kaplan will transition into a newly created board position of Lead Independent Director. CorMedix announced the appointment of Mr. Mike Seckler to the role of EVP & Chief Commercial Officer. Mr. Seckler joins CorMedix with a wealth of experience across multiple therapeutic areas including hematology and oncology, and most recently served as CEO of Evome Medical Technologies Inc. Mr. Seckler’s previous experience includes roles as COO of FerGene Inc., a Blackstone Life Sciences and Ferring Pharmaceuticals joint partnership gene therapy company, as well as head of Global Marketing and Corporate Communications for Ferring International.
내러티브 업데이트 • Jan 07CRMD: Robust Q3 Sales And Synergy Progress Will Support Further UpsideNarrative Update: CorMedix Analysts have maintained their fair value estimate for CorMedix at $19.00. Recent Street research highlights a $14.00 price target supported by what they describe as "robust" preliminary Q3 sales, better visibility into near term operating synergies, and the recent stock pullback.
분석 기사 • Dec 23CorMedix Inc.'s (NASDAQ:CRMD) 28% Jump Shows Its Popularity With InvestorsCorMedix Inc. ( NASDAQ:CRMD ) shares have had a really impressive month, gaining 28% after a shaky period beforehand...
공지 • Dec 18Cormedix Therapeutics Announces Positive Data from Ongoing Real World Evidence Study of DefencathCorMedix Therapeutics announced interim results for the Company's ongoing real-world evidence study being conducted in conjunction with U.S. Renal Care's (USRC) use of DefenCath in adult hemodialysis patients with central venous catheters. CorMedix and USRC commenced the real-world evidence study upon outpatient commercial launch in July 2024. The study is designed to demonstrate the impact of the broad use of DefenCath in a real-world setting and prospectively assess rates of catheter-related bloodstream infections (CRBSI), as well as hospitalizations secondary to these infections. The study is designed to evaluate these data points for two years. Currently, more than 3,000 patients per month are receiving DefenCath on a routine basis at USRC facilities. The company believe this data also strongly reinforces the ongoing collaborations among healthcare providers, patient advocates and elected leaders committed to transforming status quo dialysis care by addressing the long-standing and unmet need for infection prevention measures that lower hospitalizations, reduce healthcare utilization and limit costs to taxpayers. Secondary data points of missed treatment sessions, antibiotic utilization, and tPA utilization are also being assessed and may be announced with additional real-world evidence data in the future. CorMedix believes these data from this large, prospective, ongoing real-world study further underscore the LOCK-IT 100 clinical study results on which the FDA approval of DefenCath for ESRD hemodialysis patients was based. The Company expects to continue to discuss with customers and payors, such as Medicare Advantage plans, to emphasize the economic value of long-term infection prevention in these patients.
내러티브 업데이트 • Dec 14CRMD: Robust Q3 Sales Will Support Stronger Upside Momentum AheadAnalysts have modestly raised their price target on CorMedix to $19.00 from $14.00, citing robust preliminary Q3 sales, clearer visibility into near term operating synergies, and the recent stock pullback as key drivers of their more constructive outlook. Analyst Commentary Bullish Takeaways Bullish analysts highlight that robust preliminary Q3 sales provide early validation of CorMedix's commercial strategy and support the raised price target.
내러티브 업데이트 • Nov 28CRMD: Q3 Sales Strength And New Buy Rating Will Drive Momentum ForwardAnalysts have raised their price target for CorMedix to $14 from the previous level, citing stronger than expected Q3 sales and improved visibility into operational performance as key drivers of the updated outlook. Analyst Commentary Following the recent preliminary Q3 results, analysts have provided updated insights into CorMedix’s outlook, highlighting both encouraging signs and ongoing areas of caution for the company’s future performance.
내러티브 업데이트 • Nov 14CRMD: Strong Q3 Sales Will Drive Renewed Uptrend MomentumAnalysts have lowered their price target for CorMedix from $20.40 to $19.00, citing a more moderate revenue growth outlook and adjusted profit expectations. This comes despite optimism about robust Q3 sales and operational improvements.
공지 • Nov 12+ 1 more updateCorMedix Inc. Raises Earnings Guidance for the Year Ending December 31, 2025CorMedix Inc. raised earnings guidance for the year ending December 31, 2025. For the year, the company raises its full-year 2025 pro forma net revenue guidance to a range of $390 to $410 million.
공지 • Oct 31CorMedix Inc. to Report Q3, 2025 Results on Nov 12, 2025CorMedix Inc. announced that they will report Q3, 2025 results Pre-Market on Nov 12, 2025
공지 • Sep 30CorMedix Announces Completion of Enrollment in Phase III ReSPECT Clinical Trial for REZZAYOCorMedix Inc. announced completion of enrollment for the ongoing, global Phase III ReSPECT trial evaluating the efficacy of REZZAYO®? (rezafungin), a single-agent echinocandin in the prevention of Candida, Aspergillus, and Pneumocystis infection in patients undergoing allogeneic blood and marrow transplantation (BMT). This clinical trial has been sponsored by Mundipharma, located in the United Kingdom. The US distribution rights for REZZAYO were licensed under a strategic collaboration agreement with Melinta Therapeutics, LLC, a wholly owned subsidiary of CorMedix. The ReSPECT clinical trial is a Phase III, multicenter, randomized, double-blind study evaluating the efficacy and safety of once-weekly rezafungin (REZZAYO) versus a standard antimicrobial regimen (SAR) for the prevention of invasive fungal diseases (IFDs) in adults undergoing allogeneic BMT. Participants in the experimental arm receive a 400 mg loading dose of rezafungin in week one, followed by 200 mg weekly for 13 weeks, along with oral placebo matching the SAR components. The primary endpoint is fungal-free survival at day 90, with secondary objectives including incidence of IFD, discontinuation due to toxicity, and mortality adjusted for comorbidities. There are an estimated 50,000 cases of candidemia and invasive candidiasis each year in the U.S.REZZAYO is currently being studied for the prevention of invasive fun Gal diseases in adults undergoing allogeneicBMT. CorMedix estimates that there are an approximately 130,000 patients that could constitute the addressable market for antifungal prophylaxis in the U.S. and estimates an implied total addressable market ("TAM") of over $2B in this market segment. REZZAYO has orphan drug exclusivity through 2035 and patent coverage through 2038 in the U.S.
내러티브 업데이트 • Sep 04Acquisition And Pipeline Expansion Will Unlock Healthcare PotentialCorMedix’s consensus price target has edged up to $20.40, as analysts see greater revenue potential from DefenCath’s accelerating launch, expanded patient uptake, and supportive reimbursement dynamics, offsetting equity-related dilution concerns. Analyst Commentary The recent $85M equity offering extends CorMedix's cash runway but introduces dilution, prompting a reduced price target from previous levels based on valuation concerns.
공지 • Sep 03+ 2 more updatesCorMedix Inc. Announces Executive Changes, Effective August 29, 2025CorMedix Inc. announced that it has successfully completed its previously announced acquisition of Melinta Therapeutics LLC. The following executives will form the core of the senior leadership team of the newly merged company serving in roles that are the same or essentially similar to the one each executive currently holds, unless otherwise stated: Susan Blum, CFO of Melinta Therapeutics LLC, will assume the role of EVP & Chief Financial Officer; Dr. Matt David, EVP & CFO of CorMedix Inc., will assume the newly created role of EVP & Chief Business Officer; Liz Hurlburt, EVP & Chief Clinical Strategy and Operations Officer of CorMedix Inc., will assume the newly created role of EVP & Chief Operating Officer, and will serve as Chief Integration Officer; Beth Steinbrenner, SVP and Chief Human Resource Officer of CorMedix Inc., will continue in her role for the newly merged company; and Beth Zelnick Kaufman, EVP & Chief Legal and Compliance Officer and Corporate Secretary of CorMedix Inc., will continue in her role for the newly merged company.
분석 기사 • Aug 14Statutory Earnings May Not Be The Best Way To Understand CorMedix's (NASDAQ:CRMD) True PositionThe latest earnings release from CorMedix Inc. ( NASDAQ:CRMD ) disappointed investors. Our analysis found several...
분석 기사 • Aug 09It's A Story Of Risk Vs Reward With CorMedix Inc. (NASDAQ:CRMD)NasdaqGM:CRMD 1 Year Share Price vs Fair Value Explore CorMedix's Fair Values from the Community and select yours With...
공지 • Aug 08CorMedix Inc. (NasdaqGM:CRMD) agreed to acquire an unknown majority stake in Melinta Therapeutics, LLC from Deerfield Management Company, L.P. for approximately $330 million.CorMedix Inc. (NasdaqGM:CRMD) agreed to acquire an unknown majority stake in Melinta Therapeutics, LLC from Deerfield Management Company, L.P. for approximately $330 million on August 7, 2025. A cash consideration of $260 million will be paid by CorMedix Inc. As part of consideration, $325 million is paid towards common equity of Melinta Therapeutics, LLC. The transaction is subject to approval by regulatory board. The transaction is subject to the expiration or termination of the waiting period under the Hart-Scott-Rodino Antitrust Improvements Act of 1976 (the ‘HSR Act’). The Company expects the transaction to close as early as September 1, 2025. The cash consideration will be funded by a combination of the Company’s existing cash on hand and a $150 million Convertible Notes Offering Evercore Inc. acted as financial advisor for Melinta Therapeutics, LLC. Fenwick & West LLP acted as legal advisor for Melinta Therapeutics, LLC. Katten Muchin Rosenman LLP acted as legal advisor for Deerfield Management Company, L.P. Jared Fertman and Andrew Marmer of Willkie Farr & Gallagher LLP acted as legal advisor to CorMedix Inc.
공지 • Aug 07CorMedix Inc. Provides Earnings Guidance for the Full Year 2025CorMedix Inc. provided earnings guidance for the full year 2025. For the year, the company expects Pro Forma 2025 Revenue: $305 million – $335 million.
공지 • Jun 30+ 5 more updatesCorMedix Inc.(NasdaqGM:CRMD) dropped from Russell Small Cap Comp Value IndexCorMedix Inc.(NasdaqGM:CRMD) dropped from Russell Small Cap Comp Value Index
공지 • Jun 27CorMedix Inc. has completed a Follow-on Equity Offering in the amount of $85 million.CorMedix Inc. has completed a Follow-on Equity Offering in the amount of $85 million. Security Name: Common Stock Security Type: Common Stock Securities Offered: 6,604,507 Price\Range: $12.869999
분석 기사 • Jun 27Bullish: Analysts Just Made A Meaningful Upgrade To Their CorMedix Inc. (NASDAQ:CRMD) ForecastsCelebrations may be in order for CorMedix Inc. ( NASDAQ:CRMD ) shareholders, with the analysts delivering a significant...
공지 • Jun 27CorMedix Inc. has filed a Follow-on Equity Offering in the amount of $85 million.CorMedix Inc. has filed a Follow-on Equity Offering in the amount of $85 million. Security Name: Common Stock Security Type: Common Stock
공지 • Jun 24CorMedix Inc. Increases Net Sales Guidance of Second Quarter 2025CorMedix Inc. announced that as a result of this new customer implementation and other positive business developments, CorMedix is increasing its second quarter 2025 net sales guidance from the previously communicated $31 million to a range of $35 million to $40 million.
공지 • May 06CorMedix Inc. Revises Sales Guidance for the First Half of 2025CorMedix Inc. revised sales guidance for the first half of 2025. The company expected to be at the high-end of the previously announced first half net sales guidance of $62 million to $70 million, based on latest order trends and inventory tracking with current purchasing customers.
새 내러티브 • Apr 30DefenCath Launch Will Boost Inpatient And Dialysis Opportunities Strong revenue growth prospects from DefenCath's successful launch and expansion into new segments like inpatient facilities and partnerships.
공지 • Apr 29CorMedix Inc., Annual General Meeting, Jun 24, 2025CorMedix Inc., Annual General Meeting, Jun 24, 2025.
공지 • Apr 08CorMedix Inc. Raises Financial Guidance for First Half of 2025CorMedix Inc. raised financial guidance for first half of 2025. Since providing initial guidance, the Company received larger than expected orders during the final week of March, and has also obtained additional visibility into inventory levels on hand at some of its current purchasing customers. Based on this new information, CorMedix is increasing its first half 2025 guidance for Net Sales to existing purchasing customers to a revised range of $62 million to $70 million.
Seeking Alpha • Mar 26The Hidden Risks Behind CorMedix's First Profitable QuarterSummary CorMedix Inc.'s DefenCath reduces catheter infections by 71%, but the limited market potential challenges long-term adoption. Early strong revenues likely reflect inventory building rather than sustained utilization patterns. Special reimbursements boosting current profits will expire, threatening future margins and pricing power. Half-year guidance signals limited visibility, with management warning of inventory adjustments and price erosion. Monte Carlo simulations suggest CRMD faces more downside risk (25%) than upside potential (8.8%). Read the full article on Seeking Alpha
공지 • Mar 25CorMedix Inc. Provides Preliminary Earnings Guidance for the First Half of 2025CorMedix Inc. provides preliminary earnings guidance for the first half of 2025. For the year, the company expects net revenue guidance for first half of 2025 of $50– $60 million, based on the run rate of current purchasing customers, with more than $33 million expected in first quarter.
공지 • Mar 18CorMedix Inc. to Report Q4, 2024 Results on Mar 25, 2025CorMedix Inc. announced that they will report Q4, 2024 results Pre-Market on Mar 25, 2025
분석 기사 • Jan 17Here's Why We're Not Too Worried About CorMedix's (NASDAQ:CRMD) Cash Burn SituationJust because a business does not make any money, does not mean that the stock will go down. Indeed, CorMedix...
Seeking Alpha • Jan 07CorMedix: Finally In Commercialization ModeSummary CorMedix Inc.'s DefenCath, an antimicrobial catheter lock solution, shows considerable promise in reducing catheter-related bloodstream infections. The product was approved earlier this year and has seen solid initial sales traction. Analyst firms are optimistic about the company's prospects, even as the stock is down just over a third from recent highs. An analysis of CorMedix follows in the paragraphs below. Read the full article on Seeking Alpha
분석 기사 • Dec 13CorMedix Inc.'s (NASDAQ:CRMD) P/S Is On The MarkWhen you see that almost half of the companies in the Pharmaceuticals industry in the United States have price-to-sales...
분석 기사 • Nov 14Here's Why CorMedix Inc.'s (NASDAQ:CRMD) CEO Compensation Is The Least Of Shareholders' ConcernsKey Insights CorMedix to hold its Annual General Meeting on 21st of November CEO Joe Todisco's total compensation...
분석 기사 • Nov 04Analysts Just Made A Massive Upgrade To Their CorMedix Inc. (NASDAQ:CRMD) ForecastsCelebrations may be in order for CorMedix Inc. ( NASDAQ:CRMD ) shareholders, with the analysts delivering a significant...
Seeking Alpha • Oct 28CorMedix 2.0: New Leadership, New Approval, New FocusSummary CorMedix is a biopharmaceutical company that has undergone a re-birth as it enters a new phase with FDA approval of its anti-infective catheter solution, DefenCath. The company has faced challenges in the past, including management issues and regulatory delays, but now warrants a fresh look and valuation as the company executes on commercialization. DefenCath offers a unique solution for preventing catheter-related bloodstream infections, with the potential to reduce costs and save lives. Read the full article on Seeking Alpha
공지 • Oct 23CorMedix Inc. to Report Q3, 2024 Results on Oct 30, 2024CorMedix Inc. announced that they will report Q3, 2024 results on Oct 30, 2024
Seeking Alpha • Oct 19CorMedix: Delayed Approval, Low Cash, Good ProspectsSummary CorMedix's DefenCath, an FDA-approved antimicrobial catheter lock solution, significantly reduces catheter-related bloodstream infections, addressing a critical need in hemodialysis patients. DefenCath's market exclusivity and reimbursement strategies position it well in the growing $2.6bn CRBSI market, with significant potential for revenue. Despite past challenges, CorMedix's financial outlook is improving, but additional funds are needed for future trials in new indications. Investors should await Q3 earnings data for a clearer picture, as current stock spikes are driven by DefenCath's recent launch. Read the full article on Seeking Alpha
공지 • Oct 09CorMedix Inc., Annual General Meeting, Nov 21, 2024CorMedix Inc., Annual General Meeting, Nov 21, 2024.
분석 기사 • Sep 30We're Hopeful That CorMedix (NASDAQ:CRMD) Will Use Its Cash WiselyJust because a business does not make any money, does not mean that the stock will go down. For example, CorMedix...
공지 • Aug 07CorMedix Inc. to Report Q2, 2024 Results on Aug 14, 2024CorMedix Inc. announced that they will report Q2, 2024 results Pre-Market on Aug 14, 2024
공지 • May 11CorMedix Inc. has filed a Follow-on Equity Offering in the amount of $50 million.CorMedix Inc. has filed a Follow-on Equity Offering in the amount of $50 million. Security Name: Common Stock Security Type: Common Stock Transaction Features: At the Market Offering
공지 • May 08CorMedix Inc. to Report Q1, 2024 Results on May 09, 2024CorMedix Inc. announced that they will report Q1, 2024 results Pre-Market on May 09, 2024
공지 • Apr 15CorMedix Inc. Announces U.S. Inpatient Commercial Availability of DefenCath®? (Taurolidine and Heparin)CorMedix Inc. announced DefenCath®? (taurolidine and heparin) catheter lock solution (CLS) is now commercially available for U.S. inpatient use. DefenCath (taurolidine and Heparin) is approved by the U.S. Food and Drug Administration (FDA) to reduce the incidence of catheter-related bloodstream infections (CRBSIs) in adult patients with kidney failure receiving chronic hemodialysis through a central venous catheter (HD-CVC). The commencement of U.S. outpatient commercialization of DefenCath is planned for July 1, 2024. Outpatient commercial availability is contingent upon the Center for Medicare & Medicaid Services (CMS) approval and implementation of the DefenCath Transitional Drug Add-On Payment Adjustment (TDAPA) application in accordance with the agency's publicly stated objective that CMS aims for an effective date for applying the TDAPA for a particular product that is one quarter after the effective date of the HCPCS code for the product. The CMS Final HCPCS coding decision for DefenCath was published by CMS on April 2nd, establishing a new HCPCS Level II code for DefenCath, and CorMedix continues to work closely with CMS on the TDAPA implementation process.
New Risk • Apr 11New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of American stocks, typically moving 10% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Major Risk Revenue is less than US$1m. Minor Risks Share price has been volatile over the past 3 months (10% average weekly change). Shareholders have been diluted in the past year (24% increase in shares outstanding).
분석 기사 • Apr 06We Think CorMedix (NASDAQ:CRMD) Can Afford To Drive Business GrowthEven when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...
Recent Insider Transactions • Mar 15CEO & Director recently bought US$51k worth of stockOn the 13th of March, Joseph Todisco bought around 14k shares on-market at roughly US$3.74 per share. This transaction amounted to 10% of their direct individual holding at the time of the trade. This was the largest purchase by an insider in the last 3 months. Joseph has been a buyer over the last 12 months, purchasing a net total of US$111k worth in shares.
Breakeven Date Change • Mar 13Forecast breakeven date moved forward to 2025The 4 analysts covering CorMedix previously expected the company to break even in 2026. New consensus forecast suggests losses will reduce by 2.8% to 2024. The company is expected to make a profit of US$6.71m in 2025. Average annual earnings growth of 60% is required to achieve expected profit on schedule.
공지 • Mar 07CorMedix Inc. to Report Q4, 2023 Results on Mar 12, 2024CorMedix Inc. announced that they will report Q4, 2023 results Pre-Market on Mar 12, 2024
Price Target Changed • Feb 01Price target decreased by 7.0% to US$13.25Down from US$14.25, the current price target is an average from 4 analysts. New target price is 349% above last closing price of US$2.95. Stock is down 34% over the past year. The company is forecast to post a net loss per share of US$0.85 next year compared to a net loss per share of US$0.74 last year.
공지 • Jan 31CorMedix Inc. Updates Related to Its Business and Anticipated Launch of DefenCathCorMedix Inc. announced updates related to its business and anticipated launch of DefenCath. On January 25, 2024 the Center for Medicare & Medicaid Services (CMS) notified CorMedix that the agency has determined DefenCath will be eligible for reimbursement in accordance with the ESRD PPS. As such, CorMedix is entitled to submit an application for a Transitional Drug Add-On Payment (TDAPA) which currently allows for five years of additional payment reimbursement to outpatient providers. CorMedix submitted its TDAPA application on January 26 after receiving the CMS notification, and CMS has subsequently confirmed receipt. As a result of CMS' determination that DefenCath is within the scope of the ESRD PPS and eligible for TDAPA, CorMedix has established its list price (WAC) of $249.99 per 3ml vial, to account for the market dynamics and functionality of the TDAPA framework. Should CMS make a future determination that DefenCath is eligible for Medicare Part B reimbursement, CorMedix has committed to CMS to reduce the list price accordingly. CorMedix previously applied for and received a New Technology Add-On Payment (NTAP) from CMS for inpatient reimbursement of DefenCath. Now that the company has established a WAC price for commercialization, CorMedix will notify CMS accordingly to make any necessary adjustment to the NTAP reimbursement payment to inpatient facilities.
공지 • Jan 08Cormedix Inc. Announces Commercial and Operational UpdatesCorMedix Inc. announced several commercial and operational updates related to its business and anticipated launch of DefenCath®. Recent Updates: CorMedix formally submitted an HCPCS application for a J-Code to the Center for Medicare and Medicaid Services (CMS) on December 8, 2023 for DefenCath, and CMS has confirmed the application is under review. The Company continues to engage in discussions with CMS related to the appropriate outpatient reimbursement structure for DefenCath and remains committed to its pursuit of separate payment under Medicare Part B as the appropriate reimbursement mechanism for the product. In such an instance, the Company expects to establish a list price based on the market dynamics for both inpatient contracting as well as a Transitional Drug Add-On Payment (TDAPA) framework for outpatient reimbursement. CorMedix would then subsequently revise the list price downward should CMS make a determination in favor of separate payment under Medicare PartB. CorMedix expects to provide further detail on the DefenCath market opportunity as the company receive clarity from CMS regarding outpatient reimbursement. The Company believes it has sufficient cash, cash equivalents and available resources to fund the commercial launch.
Breakeven Date Change • Dec 31Forecast to breakeven in 2026The 4 analysts covering CorMedix expect the company to break even for the first time. New consensus forecast suggests the company will make a profit of US$16.6m in 2026. Average annual earnings growth of 59% is required to achieve expected profit on schedule.
공지 • Dec 16CorMedix Inc. Approves the Separation of Employment of Phoebe MountsOn December 12, 2023, upon mutual agreement between CorMedix Inc. (the “Company”) and Phoebe Mounts, Ph.D., Esq., the Company’s Executive Vice President, General Counsel and Corporate Secretary, the Board of Directors of the Company (the “Board”) approved the separation of employment of Dr. Mounts, effective December 31, 2023 (the “Termination Date”). Dr. Mounts will cease to hold the title of General Counsel and Corporate Secretary effective December 12, 2023. Until the Termination Date, Dr. Mounts will continue to serve as Executive Vice President and devote her time and attention to facilitating the transition of her duties and responsibilities.
공지 • Dec 15CorMedix Inc. Announces the Appointment of Beth Zelnick Kaufman, Esq. as Executive Vice President, Chief Legal Officer, and Corporate Secretary, Effective December 12, 2023CorMedix Inc. announced the appointment of Beth Zelnick Kaufman, Esq. as EVP, Chief Legal Officer, and Corporate Secretary, effective December 12, 2023. The Company also announced that, upon mutual agreement with the Company, Dr. Phoebe Mounts will no longer serve as the Company’s General Counsel, effective December 12, 2023, and will be separating from CorMedix effective December 31, 2023, to pursue other opportunities. Ms. Zelnick Kaufman has more than two decades of legal, compliance and operations experience in the life sciences industry. Prior to joining CorMedix, she most recently served as Chief Legal and Administrative Officer and Corporate Secretary of Akorn Pharmaceuticals, a specialty and generic pharmaceuticals company. Ms. Zelnick Kaufman also served in several roles at Amneal Pharmaceuticals, a publicly traded global generics, biosimilars and branded pharmaceuticals company, including roles as Assistant General Counsel, Vice President, Legal Affairs, and Head of Government Affairs. During her tenure at these and other pharmaceutical companies, Ms. Zelnick Kaufman gained deep experience in the pharmaceutical industry across legal, regulatory, government affairs, and other operational areas. Earlier in her career, Ms. Zelnick Kaufman held roles at Actavis, Alpharma and Topcon America and spent time as an Associate in the law firm Brown, Rudnick. Ms. Zelnick Kaufman holds a Juris Doctor degree from New York University Law School and a Bachelor of Arts degree from Amherst College.
공지 • Nov 17CorMedix Inc. Announces FDA Approval of DefenCath(R) to Reduce the Incidence of Catheter Related Bloodstream Infections in Adult Hemodialysis PatientsCorMedix Inc. announced that the U.S. Food and Drug Administration (FDA) has approved DefenCath(R) (taurolidine and heparin) catheter lock solution (CLS) to reduce the incidence of catheter-related bloodstream infections (CRBSIs) for the limited population of adult patients with kidney failure receiving chronic hemodialysis through a central venous catheter (CVC). DefenCath is the first and only FDA-approved antimicrobial CLS in the U.S. and was shown to reduce the risk of CRBSIs by up to 71% in a Phase 3 clinical study. The FDA approval of DefenCath was supported by results from the randomized, double-blind, active control, multicenter pivotal Phase 3 LOCK-IT-100 clinical trial designed to assess the efficacy and safety of DefenCath for reducing the incidence of CRBSIs in patients with kidney failure receiving chronic Hemodialysis through a central Venous catheter. The FDA approval of DefENCath was supported by results from The randomized, double-blind, Active control, multicenter pivotal Phase3 LOCK-IT-100clinical trial designed to assess the efficacy, safety of DefenCath for reduce the incidence of CRBSIs In the study, a total of 806 subjects were randomized to receive either DefenCath or heparin as a CLS. Until now, patients who need hemodialysis via a central venous catheter have had little choice other than to accept high infection risks associated with the existing standard of care. The FDA's approval of DefenCath is a meaningful moment for patients and their healthcare providers because they now have a new alternative to reduce the risks of CRBSIs. DefenCath is an antimicrobial catheter lock solution (CL S) approved by the FDA to reduce the incidence of cat catheter-related bloodstream infections ("CRBSIs") for the limited population of adult patient with kidney failure receiving chronic he modialysis through a central venal catheter (CVC). In addition, FDA designated DefenCath as a Qualified Infectious Disease Product (QIDP) established by the Generating Antibiotic Incentives Now (GAIN) Act that supports development of antibacterial and antifungal products that treat serious or life-threatening infections. DefenCath has been designated by FDA as Fast-up, and FDA as Fast-up, a novel, non-antibiotic antimicrobial antimicrobial solution designed to prevent costly and life-threatening bloodstream infections associated with the use of central venous catheters in patients undergoing chronic hemodialysis. DefenCath has been identified by FDA as Fast-up and FDA as Fast-up and a Phase 3 clinical study.
Reported Earnings • Nov 16Third quarter 2023 earnings released: US$0.17 loss per share (vs US$0.17 loss in 3Q 2022)Third quarter 2023 results: US$0.17 loss per share (further deteriorated from US$0.17 loss in 3Q 2022). Net loss: US$9.74m (loss widened 42% from 3Q 2022). Revenue is forecast to grow 58% p.a. on average during the next 3 years, compared to a 8.4% growth forecast for the Pharmaceuticals industry in the US. Over the last 3 years on average, earnings per share has fallen by 3% per year but the company’s share price has fallen by 20% per year, which means it is performing significantly worse than earnings.
공지 • Nov 03CorMedix Inc. to Report Q3, 2023 Results on Nov 14, 2023CorMedix Inc. announced that they will report Q3, 2023 results After-Market on Nov 14, 2023
분석 기사 • Nov 02We're Hopeful That CorMedix (NASDAQ:CRMD) Will Use Its Cash WiselyEven when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...
공지 • Sep 14CorMedix Inc., Annual General Meeting, Oct 26, 2023CorMedix Inc., Annual General Meeting, Oct 26, 2023, at 09:00 US Eastern Standard Time. Agenda: To elect seven directors to serve until the 2024 Annual Meeting of Stockholders and until their successors are duly elected and qualified; to approve on a non-binding advisory basis the compensation of company's named executive officers for 2022; to ratify the appointment of Marcum LLP as company's independent registered public accounting firm for the fiscal year ending December 31, 2023; and to act upon such other matters as may properly come before the meeting or any adjournment, postponement or continuation thereof.
공지 • Aug 18Cormedix Inc. Announces Resignation of Paulo F. Costa as Member of the Board of Directors, Effective as of October 15, 2023CorMedix Inc. announced that Paulo F. Costa, a member of the Board of Directors notified the Board that he will be retiring from the Board, effective as of October 15, 2023. The Company does not intend to fill Mr. Costa’s seat on the Board at this time and therefore the size of the Board will be reduced to seven directors effective as of October 15, 2023. The Company expressed gratitude to Mr. Costa for his contributions to the Board and the Company. Mr. Costa’s departure is not as a result of any dispute or disagreement with the Company, its management, the Board, or any matter relating to the Company’s operations, policies or practices. The Board is evaluating how it intends to fill Mr. Costa’s committee assignment.
Price Target Changed • Aug 11Price target decreased by 18% to US$13.75Down from US$16.67, the current price target is an average from 4 analysts. New target price is 212% above last closing price of US$4.40. Stock is up 6.0% over the past year. The company is forecast to post a net loss per share of US$1.02 next year compared to a net loss per share of US$0.74 last year.
Reported Earnings • Aug 08First half 2023 earnings released: US$0.49 loss per share (vs US$0.38 loss in 1H 2022)First half 2023 results: US$0.49 loss per share (further deteriorated from US$0.38 loss in 1H 2022). Net loss: US$21.8m (loss widened 49% from 1H 2022). Revenue is forecast to grow 61% p.a. on average during the next 3 years, compared to a 7.1% growth forecast for the Pharmaceuticals industry in the US. Over the last 3 years on average, earnings per share has increased by 15% per year but the company’s share price has only increased by 3% per year, which means it is significantly lagging earnings growth.
분석 기사 • Jul 31Here's Why We're Not Too Worried About CorMedix's (NASDAQ:CRMD) Cash Burn SituationEven when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...
공지 • Jul 28CorMedix Inc. to Report Q2, 2023 Results on Aug 08, 2023CorMedix Inc. announced that they will report Q2, 2023 results Pre-Market on Aug 08, 2023
공지 • Jun 22CorMedix Inc. Announces FDA Acceptance of Resubmission of New Drug Application for DefenCathCorMedix Inc. announced that the resubmission of the New Drug Application (NDA) for DefenCath has been accepted for filing by the U.S. Food and Drug Administration (FDA). The Agency considers the resubmission as a complete, Class 2 response with a six-month review, and has assigned a Prescription Drug User Fee Act (PDUFA) target action date of November 15, 2023. DefenCath is being developed as a catheter lock solution with an initial indication of use for the reduction of catheter-related bloodstream infections (CRBSIs) in patients with kidney failure who are receiving chronic hemodialysis via a central venous catheter.
공지 • May 17Cormedix Inc. Announces Resubmission of New Drug Application for DefencathCorMedix Inc. announced that the New Drug Application for DefenCath was resubmitted to the U.S. Food and Drug Administration, and the submission has been acknowledged as received for processing.
Reported Earnings • May 17First quarter 2023 earnings released: US$0.24 loss per share (vs US$0.18 loss in 1Q 2022)First quarter 2023 results: US$0.24 loss per share (further deteriorated from US$0.18 loss in 1Q 2022). Net loss: US$10.6m (loss widened 50% from 1Q 2022). Revenue is forecast to grow 199% p.a. on average during the next 2 years, compared to a 7.1% growth forecast for the Pharmaceuticals industry in the US. Over the last 3 years on average, earnings per share has increased by 27% per year but the company’s share price has only increased by 3% per year, which means it is significantly lagging earnings growth.
공지 • May 09CorMedix Inc. to Report Q1, 2023 Results on May 15, 2023CorMedix Inc. announced that they will report Q1, 2023 results at 4:00 PM, US Eastern Standard Time on May 15, 2023
Reported Earnings • Mar 31Full year 2022 earnings: Revenues exceed analysts expectations while EPS lags behindFull year 2022 results: US$0.74 loss per share. Net loss: US$29.7m (loss widened 5.3% from FY 2021). Revenue exceeded analyst estimates. Earnings per share (EPS) missed analyst estimates by 1.4%. Revenue is forecast to grow 56% p.a. on average during the next 3 years, compared to a 5.1% growth forecast for the Pharmaceuticals industry in the US.
분석 기사 • Feb 25CorMedix (NASDAQ:CRMD) Is In A Good Position To Deliver On Growth PlansJust because a business does not make any money, does not mean that the stock will go down. For example, although...
공지 • Jan 18Cormedix Inc. Announces Promotions in Commercial and Tech OpsCorMedix Inc. announced the following promotions within the organization: Erin Miststry, SVP Commercial, has been promoted to EVP and Chief Commercial Officer. Ms. Mistry will have oversight and responsibility for all commercial launch strategy for DefenCath and the build out of launch infrastructure, including but not limited to market access, commercial operations and field-based sales personnel. Ms. Mistry joined CorMedix 2020 and has been an integral architect of the company's go to market and reimbursement strategy. Dr. Tushar Mukherjee, VP of Technical Operations has been promoted to SVP, Head of Technical Operations. Dr. Mukherjee joined CorMedix in early 2022 and has been a valuable leader and contributor for the technical team. In his new role, Dr. Mukherjee will report directly to the CEO and will assume responsibility for the final validation of all manufacturing, packaging and analytical testing of DefenCath, as well as all technical reviews of new product opportunities. Dr. Phoebe Mounts who had previously assumed interim oversight of technical operations will remain with the organization in her critical role as General Counsel and Head of Regulatory Affairs.
Recent Insider Transactions • Nov 18CEO & Director recently bought US$76k worth of stockOn the 15th of November, Joseph Todisco bought around 20k shares on-market at roughly US$3.82 per share. This transaction increased Joseph's direct individual holding by 1x at the time of the trade. This was the largest purchase by an insider in the last 3 months. Joseph has been a buyer over the last 12 months, purchasing a net total of US$129k worth in shares.
Price Target Changed • Nov 16Price target increased to US$15.00Up from US$14.00, the current price target is an average from 3 analysts. New target price is 307% above last closing price of US$3.69. Stock is down 29% over the past year. The company is forecast to post a net loss per share of US$0.73 next year compared to a net loss per share of US$0.75 last year.
Reported Earnings • Nov 16Third quarter 2022 earnings released: US$0.17 loss per share (vs US$0.23 loss in 3Q 2021)Third quarter 2022 results: US$0.17 loss per share (improved from US$0.23 loss in 3Q 2021). Net loss: US$6.85m (loss narrowed 20% from 3Q 2021). Revenue is forecast to grow 79% p.a. on average during the next 3 years, compared to a 3.8% growth forecast for the Pharmaceuticals industry in the US. Over the last 3 years on average, earnings per share has increased by 36% per year but the company’s share price has fallen by 18% per year, which means it is significantly lagging earnings.