Nymox Pharmaceutical（NYMX.F）株式概要ナイモックス・ファーマシューティカル・コーポレーション（Nymox Pharmaceutical Corporation）はバイオ医薬品会社で、カナダ、米国、欧州で高齢化社会向け製品の研究開発に従事している。 詳細NYMX.F ファンダメンタル分析スノーフレーク・スコア評価0/6将来の成長0/6過去の実績0/6財務の健全性0/6配当金0/6リスク分析マイナスの株主資本 収益が 100 万ドル未満 ( $0 )最新の財務報告は1年以上前のものである US市場と比較して、過去 3 か月間の株価の変動が非常に大きい+1 さらなるリスクすべてのリスクチェックを見るNYMX.F Community Fair Values Create NarrativeSee what others think this stock is worth. Follow their fair value or set your own to get alerts.Your Fair ValueUS$Current PriceUS$0.09該当なし内在価値ディスカウントEst. Revenue$PastFuture-18m3m2016201920222025202620282031Revenue US$1.0Earnings US$0.2AdvancedSet Fair ValueView all narrativesNymox Pharmaceutical Corporation 競合他社Ernexa TherapeuticsSymbol: NasdaqCM:ERNAMarket cap: US$9.2mAdaptimmune TherapeuticsSymbol: OTCPK:ADAP.YMarket cap: US$9.0mKairos PharmaSymbol: NYSEAM:KAPAMarket cap: US$9.4mAprea TherapeuticsSymbol: NasdaqCM:APREMarket cap: US$8.9m価格と性能株価の高値、安値、推移の概要Nymox Pharmaceutical過去の株価現在の株価US$0.0952週高値US$0.2052週安値US$0.03ベータ12.771ヶ月の変化156.41%3ヶ月変化77.51%1年変化-10.00%3年間の変化-76.82%5年間の変化-94.71%IPOからの変化-98.58%最新ニュースお知らせ • May 02Nymox Pharmaceutical Corporation announced delayed 20-F filingOn 05/01/2025, Nymox Pharmaceutical Corporation announced that they will be unable to file their next 20-F by the deadline required by the SEC.お知らせ • Mar 27Nymox Pharmaceutical Corporation Reports Victory in Bahamas Litigation Against Terminated Ex-Employees – Court Awards Costs and DamagesNymox Pharmaceutical Corporation reported that the Bahamas Supreme Court has issued a formal Order officially putting an end to the Bahamas litigation brought by terminated ex-employees. The Order also awards to Nymox its costs incurred in defending the ill-conceived lawsuit, as well as damages Nymox has suffered as a result of the litigation. The Court order states the following: The Interim Injunction Order is set aside; The damages caused to the Company shall be assessed by a Registrar and paid by the Claimants (the persons who filed the lawsuit); and The Claimants shall pay the Company’s net costs for the entire Action. This is the first of more than one action by and between the Company and Randall Lanham, (former General Counsel for Nymox), Chris Riley, (former short-term CFO), Richard Cutler (former external Counsel and member of Board), and their financial backers.お知らせ • Sep 26Nymox Pharmaceutical Corporation Announces Submission of New Marketing Authorization Application Submission for NYMOZARFEX (TM) for BPHNymox Pharmaceutical Corporation announced that a new formal submission has been made by the company in the U.K. for Nymozarfex (TM) for the treatment of benign prostatic hyperplasia (BPH). The Marketing Authorization Application (MAA) was submitted to the U.K. Medicines & Healthcare products Regulatory Agency (MHRA). The new submission includes England, Wales, Scotland and Northern Ireland. The company will provide further information, including with respect to other submissions for Nymozarfex (TM), when the information becomes available.お知らせ • Sep 08The Nasdaq Stock Market to Delist the Common Stock of Nymox PharmaceuticalThe Nasdaq Stock Market announced that it will delist the common stock of Nymox Pharmaceutical Corporation. Nymox Pharmaceutical Corporation’s securities were suspended on July 7, 2023, and have not traded on Nasdaq since that time.お知らせ • Aug 03Nymox Pharmaceutical Corporation announced that it expects to receive $2 million in fundingNymox Pharmaceutical Corporation announced a private placement of 2,000,000 common shares at a price of $1.00 per share for gross proceeds of $2,000,000 on August 2, 2023. The company will also issue 500,000 warrants. The transaction included participation from James G. Robinson, an independent director of the company. The investment will close in the upcoming days after the customary formalities are completed.お知らせ • Jul 26Nymox Pharmaceutical Corporation Reports Successful New NYMOZARFEX (TM) Long-Term Prostate Cancer Treatment Clinical Trial ResultsNymox Pharmaceutical Corporation announced important new long-term clinical trial results from the company's 146 patient NX03-0040 NYMOZARFEX (TM) U.S. study for low grade localized prostate cancer. New long-term follow-up data from the prospective randomized clinical trial of NYMOZARFEX (TM) for low grade early prostate cancer has indicated that there is strong statistically significant benefit from the treatment compared to controls when all available patient outcomes were included from 18 months to as long as up to >10 years after treatment. These additional 5 to 10-year data points add to the 5-year data that was published in the peer review World Journal of Urology in 2020 (World J Urol 38, 3101–3111 (2020). All clinical trial sites that were still open were contacted for follow-up data on the prostate cancer status of all available patients. A full effort was made to reach all possible subjects. The outcome comparisons showed greatly reduced percentages of subjects treated with NYMOZARFEX (TM) who had progressed by either cancer grade worsening or by prostate cancer surgery, radiotherapy, or chemotherapy; and which remained overall strongly statistically significant compared to the study's randomized controls (p<.01). This unique and successful study is the world's first and only long-term prospective randomized controlled study of an intraprostatic molecular injectable treatment for low-grade localized prostate cancer to have been accomplished. The new data represents the longest term data available from this major study. Study NX03-0040 was undertaken starting in 2012 at investigational sites across the U.S. with 146 men with the biopsy confirmed diagnosis of Grade Group1 prostate cancer. NYMOZARFEX (TM) was administered by a single painless injection directly into the prostate in a relatively simple procedure requiring several minutes or less in an office setting without sedation or anesthesia, and guided by routine ultrasound. NYMOZARFEX (TM) was injected into the area of the prostate where the cancer was previously detected prior to enrollment in NX03-0040. The patients were then biopsied after 6 weeks and then every 18 months, along with serial PSA measurements and long-term follow-up. All subjects with 18 months or more follow-up were compared with the inclusion of follow-up data from up to 10 years or more after a single injection of NYMOZARFEX (TM). For the patients where investigational sites were closed or where patients for unrelated reasons were no longer available, the last known status reports were included if they were 18 months or longer. For any subject with a worsening (increase) in grade of prostate cancer on biopsy; or with prostate cancer surgery, or radiotherapy or chemotherapy, they were included regardless of time after study treatment, and were counted in the calculation as treatment failures. The data shows that the number of patients with one focal injection of NYMOZARFEX (TM) 15 mg directed at the tumor had significantly less progression to more advanced cancer or to major cancer treatments, than the randomized control subjects followed in the study. Low grade localized prostate cancer (Gleason 3+3; T1c) is a very common treatment problem. The Nymox study reported involves patients with initially Gleason grade 3+3 or lower. These patients are found to have these tumors by biopsy which is usually instituted after finding abnormalities in PSA levels, and/or after abnormal digital rectal examination of the prostate, and/or after the patient has experienced lower urinary tract symptoms or other changes. Low grade localized prostate cancer represents a therapeutic challenge. Because of its slow growth and low initial level of malignancy, urologists and patients can be reluctant to proceed to invasive surgical treatments or radiotherapy due to the unpleasant and often permanent side effects these treatments cause in the genitourinary tract, such as sexual functional issues and/or urinary issues. Eventually if and when the tumor progresses, invasive surgical and/or radiotherapeutic procedures become necessary, with greater risk due to the progression. Occasionally the tumors become highly malignant after variable lengths of time. These risks cause understandable anxieties and distress and many men prefer to advance to invasive therapy before running these risks of higher grade cancers. It is widely acknowledged that a treatment like NYMOZARFEX (TM) that can destroy or ablate the low grade cancers of the prostate without the dreaded side effects and morbidities, would be an important benefit for these patients. Prostate cancer is the most commonly diagnosed cancer in men, other than skin cancer, and is the second leading cause of cancer death for men. Approximately 50% of prostate cancers are initially considered low risk. One of the major problems with the main current prostate treatments for localized prostate cancer (radical prostatectomy, external beam radiation, brachytherapy) is the relatively high incidence of serious sexual and other problems post- treatment. In 9 studies, NYMOZARFEX (TM) treatment has been shown to have a negligible significant adverse effect profile post-treatment and no significant adverse effects on sexual or other functions or testosterone levels. Leading urologists have long recognized the unmet need for prostate cancer treatments that can contribute to improved outcomes for their patients together with reduced side effects and stresses that may have significantly impact on quality of life. The goal of NYMOZARFEX (TM) injectable is to allow for an initial and less toxic treatment for low-risk prostate cancer patients, achieving the benefits of molecular ablation with minimal risk of side effects. For many patients, this treatment combined with surveillance would be extremely helpful for the unpleasant and persistent uncertainties, anxieties, and psychological/emotional burdens associated with only selecting active surveillance.最新情報をもっと見るRecent updatesお知らせ • May 02Nymox Pharmaceutical Corporation announced delayed 20-F filingOn 05/01/2025, Nymox Pharmaceutical Corporation announced that they will be unable to file their next 20-F by the deadline required by the SEC.お知らせ • Mar 27Nymox Pharmaceutical Corporation Reports Victory in Bahamas Litigation Against Terminated Ex-Employees – Court Awards Costs and DamagesNymox Pharmaceutical Corporation reported that the Bahamas Supreme Court has issued a formal Order officially putting an end to the Bahamas litigation brought by terminated ex-employees. The Order also awards to Nymox its costs incurred in defending the ill-conceived lawsuit, as well as damages Nymox has suffered as a result of the litigation. The Court order states the following: The Interim Injunction Order is set aside; The damages caused to the Company shall be assessed by a Registrar and paid by the Claimants (the persons who filed the lawsuit); and The Claimants shall pay the Company’s net costs for the entire Action. This is the first of more than one action by and between the Company and Randall Lanham, (former General Counsel for Nymox), Chris Riley, (former short-term CFO), Richard Cutler (former external Counsel and member of Board), and their financial backers.お知らせ • Sep 26Nymox Pharmaceutical Corporation Announces Submission of New Marketing Authorization Application Submission for NYMOZARFEX (TM) for BPHNymox Pharmaceutical Corporation announced that a new formal submission has been made by the company in the U.K. for Nymozarfex (TM) for the treatment of benign prostatic hyperplasia (BPH). The Marketing Authorization Application (MAA) was submitted to the U.K. Medicines & Healthcare products Regulatory Agency (MHRA). The new submission includes England, Wales, Scotland and Northern Ireland. The company will provide further information, including with respect to other submissions for Nymozarfex (TM), when the information becomes available.お知らせ • Sep 08The Nasdaq Stock Market to Delist the Common Stock of Nymox PharmaceuticalThe Nasdaq Stock Market announced that it will delist the common stock of Nymox Pharmaceutical Corporation. Nymox Pharmaceutical Corporation’s securities were suspended on July 7, 2023, and have not traded on Nasdaq since that time.お知らせ • Aug 03Nymox Pharmaceutical Corporation announced that it expects to receive $2 million in fundingNymox Pharmaceutical Corporation announced a private placement of 2,000,000 common shares at a price of $1.00 per share for gross proceeds of $2,000,000 on August 2, 2023. The company will also issue 500,000 warrants. The transaction included participation from James G. Robinson, an independent director of the company. The investment will close in the upcoming days after the customary formalities are completed.お知らせ • Jul 26Nymox Pharmaceutical Corporation Reports Successful New NYMOZARFEX (TM) Long-Term Prostate Cancer Treatment Clinical Trial ResultsNymox Pharmaceutical Corporation announced important new long-term clinical trial results from the company's 146 patient NX03-0040 NYMOZARFEX (TM) U.S. study for low grade localized prostate cancer. New long-term follow-up data from the prospective randomized clinical trial of NYMOZARFEX (TM) for low grade early prostate cancer has indicated that there is strong statistically significant benefit from the treatment compared to controls when all available patient outcomes were included from 18 months to as long as up to >10 years after treatment. These additional 5 to 10-year data points add to the 5-year data that was published in the peer review World Journal of Urology in 2020 (World J Urol 38, 3101–3111 (2020). All clinical trial sites that were still open were contacted for follow-up data on the prostate cancer status of all available patients. A full effort was made to reach all possible subjects. The outcome comparisons showed greatly reduced percentages of subjects treated with NYMOZARFEX (TM) who had progressed by either cancer grade worsening or by prostate cancer surgery, radiotherapy, or chemotherapy; and which remained overall strongly statistically significant compared to the study's randomized controls (p<.01). This unique and successful study is the world's first and only long-term prospective randomized controlled study of an intraprostatic molecular injectable treatment for low-grade localized prostate cancer to have been accomplished. The new data represents the longest term data available from this major study. Study NX03-0040 was undertaken starting in 2012 at investigational sites across the U.S. with 146 men with the biopsy confirmed diagnosis of Grade Group1 prostate cancer. NYMOZARFEX (TM) was administered by a single painless injection directly into the prostate in a relatively simple procedure requiring several minutes or less in an office setting without sedation or anesthesia, and guided by routine ultrasound. NYMOZARFEX (TM) was injected into the area of the prostate where the cancer was previously detected prior to enrollment in NX03-0040. The patients were then biopsied after 6 weeks and then every 18 months, along with serial PSA measurements and long-term follow-up. All subjects with 18 months or more follow-up were compared with the inclusion of follow-up data from up to 10 years or more after a single injection of NYMOZARFEX (TM). For the patients where investigational sites were closed or where patients for unrelated reasons were no longer available, the last known status reports were included if they were 18 months or longer. For any subject with a worsening (increase) in grade of prostate cancer on biopsy; or with prostate cancer surgery, or radiotherapy or chemotherapy, they were included regardless of time after study treatment, and were counted in the calculation as treatment failures. The data shows that the number of patients with one focal injection of NYMOZARFEX (TM) 15 mg directed at the tumor had significantly less progression to more advanced cancer or to major cancer treatments, than the randomized control subjects followed in the study. Low grade localized prostate cancer (Gleason 3+3; T1c) is a very common treatment problem. The Nymox study reported involves patients with initially Gleason grade 3+3 or lower. These patients are found to have these tumors by biopsy which is usually instituted after finding abnormalities in PSA levels, and/or after abnormal digital rectal examination of the prostate, and/or after the patient has experienced lower urinary tract symptoms or other changes. Low grade localized prostate cancer represents a therapeutic challenge. Because of its slow growth and low initial level of malignancy, urologists and patients can be reluctant to proceed to invasive surgical treatments or radiotherapy due to the unpleasant and often permanent side effects these treatments cause in the genitourinary tract, such as sexual functional issues and/or urinary issues. Eventually if and when the tumor progresses, invasive surgical and/or radiotherapeutic procedures become necessary, with greater risk due to the progression. Occasionally the tumors become highly malignant after variable lengths of time. These risks cause understandable anxieties and distress and many men prefer to advance to invasive therapy before running these risks of higher grade cancers. It is widely acknowledged that a treatment like NYMOZARFEX (TM) that can destroy or ablate the low grade cancers of the prostate without the dreaded side effects and morbidities, would be an important benefit for these patients. Prostate cancer is the most commonly diagnosed cancer in men, other than skin cancer, and is the second leading cause of cancer death for men. Approximately 50% of prostate cancers are initially considered low risk. One of the major problems with the main current prostate treatments for localized prostate cancer (radical prostatectomy, external beam radiation, brachytherapy) is the relatively high incidence of serious sexual and other problems post- treatment. In 9 studies, NYMOZARFEX (TM) treatment has been shown to have a negligible significant adverse effect profile post-treatment and no significant adverse effects on sexual or other functions or testosterone levels. Leading urologists have long recognized the unmet need for prostate cancer treatments that can contribute to improved outcomes for their patients together with reduced side effects and stresses that may have significantly impact on quality of life. The goal of NYMOZARFEX (TM) injectable is to allow for an initial and less toxic treatment for low-risk prostate cancer patients, achieving the benefits of molecular ablation with minimal risk of side effects. For many patients, this treatment combined with surveillance would be extremely helpful for the unpleasant and persistent uncertainties, anxieties, and psychological/emotional burdens associated with only selecting active surveillance.お知らせ • Jul 13Nymox Pharmaceutical Corporation Appoints Patrick Doody as Vice President, General Counsel and Member of Board of DirectorsNymox Pharmaceutical Corporation announced the appointment of Patrick Doody as Vice President, General Counsel, and Member of Board of Directors. Mr. Doody joins Nymox from Pillsbury Winthrop Shaw Pittman LLP, where he was a partner in the Intellectual Property Group, and currently is Senior Counsel. Mr. Doody is a well-respected patent attorney with significant knowledge and experience in post-grant proceedings, patent infringement litigation, patent prosecution, licensing, opinions, and counseling. Mr. Doody has represented Nymox and its predecessor company in intellectual property matters for over 30 years, securing hundreds of issued patents for Nymox throughout the world. Mr. Doody is a former patent examiner, former in-house counsel for Union Carbide Corporation, former partner at Tier 1, AMLAW 100 firms, and also is an adjunct professor of patent law at the George Washington University School of Law. Mr. Doody obtained his BS degree in Chemical Engineering from Virginia Tech, and his law degree from the Scalia School of Law (formerly George Mason School of Law), has served in a number of leadership positions in various intellectual property associations, is ranked Band 2 by Chambers for Intellectual Property, and AV ranked by Martindale Hubbell. Much of Mr. Doodys legal career has involved counseling biotechnology, pharmaceutical, and chemical companies on all aspects of intellectual property law.お知らせ • Jul 06Nymox Delisting from NASDAQNymox Pharmaceutical Corporation (the “Company”) received a Nasdaq Hearing Delist Decision, noting that Nymox has not regained the required $1.00 share price within the 6-month extension period granted by Nasdaq, and hence the Company's shares will be suspended from trading on NASDAQ at the open of business on July 7, 2023. Nymox shares will be moved to the OTC market. The mechanics of trading the stock remain the same, as do the Company's business fundamentals. Nymox is in the process of submitting applications for the approval to market the Company's first in class drug NYMOZARFEX to treat the symptoms of benign prostatic hyperplasia (BPH). BPH is one of the most common conditions affecting middle aged and elderly men throughout the world. BPH can be devastating to men who suffer from the condition. Current treatments are associated with numerous intolerable side effects including sexual problems, such as impotence and retrograde ejaculation. Medications for BPH have been associated with prostate cancer, depression, gynecomastia and other adverse effects. The majority of men stop taking the available medications due to these and other problems. Surgery is often needed for advanced BPH. Surgery is usually effective but it is not without risks, the discomforts of surgery, and BPH surgery has side effects such as permanent retrograde ejaculation for many patients. Nymozarfex was submitted to the Danish authorities in December 2022 and the application was accepted for review in early 2023 and is currently undergoing review. The Company announced that another submission was expected to be submitted for approval in another jurisdiction in the second quarter of 2023. It is expected to be submitted in the near future and the Company will provide the appropriate update when that occurs.New Risk • Jul 01New major risk - Share price stabilityThe company's share price has been highly volatile over the past 3 months. It is more volatile than 90% of American stocks, typically moving 15% a week. This is considered a major risk. Share price volatility 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. It may also indicate 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. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-US$2.0m free cash flow). Share price has been highly volatile over the past 3 months (15% average weekly change). Negative equity (-US$1.8m). Revenue is less than US$1m. Minor Risk Market cap is less than US$100m (US$17.3m market cap).お知らせ • Dec 06Nymox Pharmaceutical Corporation Announces New Marketing Submission for Nymozarfex for BPHNymox Pharmaceutical Corporation announced that a new formal submission has been made by the Company in Europe for Fexapotide Triflutate for the treatment of benign prostatic hyperplasia (BPH). The trademarked name for the product in the application is NYMOZARFEX (TM). The Marketing Authorization Application (MAA) was submitted to the Danish authorities. The Company will provide further information, including other expected submissions, when the information becomes available.お知らせ • Nov 17Nymox Pharmaceutical Corporation, Annual General Meeting, Dec 12, 2022Nymox Pharmaceutical Corporation, Annual General Meeting, Dec 12, 2022, at 04:30 Eastern Daylight. Location: Margaritaville Resorts, Nassau Bahamas, Number Two Bay St Nasssau Bahamas Agenda: To receive the annual report of the directors, the financial statements of the corporation for the fiscal year ended December 31, 2021 and the auditors’ report thereon; to elect the directors of the corporation; to appoint the auditors of the corporation and to authorize the board of directors to fix their remuneration; to ratify the acts of the members of the board of directors for the fiscal year ending 2021; and, up and to the date of this meeting; to transact such other matters as may properly be brought before the meeting, or any adjournment thereof.Board Change • Nov 16Insufficient new directorsNo new directors have joined the board in the last 3 years. The company's board is composed of: No new directors. 2 experienced directors. 3 highly experienced directors. Lead Independent Director Rich Cutler was the last director to join the board, commencing their role in 2015. The company’s insufficient board refreshment is considered a risk according to the Simply Wall St Risk Model.Seeking Alpha • Sep 13Nymox gets FDA feedback on NDA resubmission for lead assetNymox Pharmaceutical (NASDAQ:NYMX), a biotech focused on drugs for the elderly, announced Tuesday that during the recent interactions, the FDA specified what additional information is required to resubmit a marketing application for its lead candidate Fexapotide. The company added that it is preparing the requested documentation in anticipation of the resubmission and looks forward to additional regulatory guidance from the FDA. In addition, NYMX announced plans to submit regulatory filings for Fexapotide in Q4 to seek European approval for the injection. Fexapotide Triflutate, also known as NX-1207, has undergone clinical studies for prostate-linked indications, including a Phase 3 trial for benign prostatic hyperplasia (BPH). However, in May, the company said that the FDA rejected to review the company’s marketing application for the drug in BPH.分析記事 • Aug 17Is Nymox Pharmaceutical (NASDAQ:NYMX) In A Good Position To Deliver On Growth Plans?We can readily understand why investors are attracted to unprofitable companies. For example, although Amazon.com made...お知らせ • Jul 15NYMOX Receives Deficiency Letter from NASDAQNymox Pharmaceutical Corporation (NASDAQ: NYMX) reported that on July 7, 2022 the Company received a deficiency letter from NASDAQ stating that the Company is no longer in compliance with Nasdaq Listing Rule 5550(a)(2). The Nasdaq letter states that the Company will be afforded 180 calendar days to regain compliance with the minimum bid price requirement. In order to regain compliance, the Company must have a closing bid price of $1.00 or more for a minimum of 10 consecutive business days. If at any time during this 180-day period the Company’s closing bid price meets or exceeds $1.00 for a minimum of 10 consecutive business days, Nasdaq will provide written confirmation of compliance and the matter will be closed. If the Company has not regained compliance by the expiration of the initial 180 calendar days, Nasdaq will then provide written notification to the Company that its ordinary shares are subject to delisting. At that time, the Company may appeal Nasdaq’s delisting determination to a Nasdaq Listing Qualifications Panel.Seeking Alpha • Jul 14NYMOX stock down 7.2% after receiving non-compliance letter from NasdaqNymox Pharma (NASDAQ:NYMX) is down 7.2% after the company said it received a deficiency letter from Nasdaq stating that the company is no longer in compliance with Nasdaq. The company said it has 180 calendar days to regain compliance with the minimum bid price requirement. To regain compliance, the Company must have a closing bid price of $1.00 or more for a minimum of 10 consecutive business days.お知らせ • Jul 09Nymox Pharmaceutical Corporation Announces Resignation of Erik Danielsen as Chief Financial OfficerNymox Pharmaceutical Corporation announced effective June 28, 2022, accepted the resignation of Erik Danielsen as Chief Financial Officer of the Company.お知らせ • May 24NYMOX Receives RTF letter from FDANymox Pharmaceutical Corporation received a Refusal to File letter from FDA on May 20 at 2:48 pm EST, with regard to the Company's New Drug Application (“NDA”) for Fexapotide Triflutate. Nymox’s position is that clarifications remain to be resolved at a follow-up meeting and that some significant inconsistencies were involved. The letter referred to a new outstanding issue of longer-term safety data and indicated that Nymox needed to have longer-term safety data in its NDA. Longer-term full safety data (as long as 6 years after a single low dose non-systemic injection given one time only) was not requested by the FDA in any previous pre-NDA communications. The Company's position is that Fexapotide safety profile is superior to any other conventional BPH treatment. 2. Fexapotide is a local injection with no detectable drug outside of prostate in patients after treatment. For a single injection (ie, given only one time) low dose local administration treatment, typical human clinical safety data duration requirements for approvals are in the few months range or less. Animal testing requirements are generally 2 weeks. 3. The FDA agreed at the end of Phase 2 that for eventual approval one-year safety data after a single injection of fexapotide 2.5 mg was adequate for Phase 3 pivotal studies, for clinical safety duration requirements. In Nymox pivotal Phase 3 trials 0017 and 0018, this data was achieved, and 12-month full safety data was provided in the NDA. The FDA provided detailed safety requests at the fexapotide pre-NDA meeting, which categorically did not include a longer-term clinical safety data request for fexapotide. 5. In addition, the NDA does include even longer-term (2-3 years) full safety data for fexapotide from n=344 subjects in Phase 3 Studies NX02-0020 and NX02-0022. There is no evidence of any long-term adverse safety outcomes in the pivotal study data for fexapotide.Board Change • Apr 27Insufficient new directorsNo new directors have joined the board in the last 3 years. The company's board is composed of: No new directors. 2 experienced directors. 3 highly experienced directors. Lead Independent Director Rich Cutler was the last director to join the board, commencing their role in 2015. The company’s insufficient board refreshment is considered a risk according to the Simply Wall St Risk Model.お知らせ • Mar 05Nymox Pharmaceutical Corporation Announces Submission of New Drug Application to the FDA for Fexapotide TriflutateNymox Pharmaceutical Corporation announced that it has submitted the Company’s New Drug Application (NDA) to the FDA for Fexapotide Triflutate to seek marketing approval in the U.S. for Fexapotide Triflutate for the treatment of men with benign prostatic hyperplasia (BPH). The submission of the application does not involve any guarantees or forward looking statements regarding outcomes of the submission. The Company will continue to make updates on all material and required developments with the application, and in accordance with prior statements provided in the Company’s regular SEC filings. Nymox intends to submit applications in other major markets in the near term and will provide updates at the appropriate times in due course.お知らせ • Jun 28+ 6 more updatesNymox Pharmaceutical Corporation(NasdaqCM:NYMX) dropped from Russell 3000E Value IndexNymox Pharmaceutical Corporation(NasdaqCM:NYMX) dropped from Russell 3000E Value Indexお知らせ • Apr 29Nymox Pharmaceutical Corporation announced that it expects to receive $7.999998 million in fundingNymox Pharmaceutical Corporation (NasdaqCM:NYMX) announced that it hsa entered in to definitive agreement for 3,669,724 shares at a price of $2.18 per share and warrants for the gross proceeds of $7,999,998.32? on April 28, 2021. Warrants issue in the transaction can be exercised in to 1,834,862 shares at a an exercise price of $2.50 per share and will expire five years from the date of issuance. The transaction is expected to close on or about April 30, 2021, subject to the satisfaction of customary closing conditions. The transaction is being made pursuant to the exemption from securities registration afforded by Section 4(a)(2) of the Securities Act of 1933, as amended, and Rule 506 of Regulation D as promulgated by the United States Securities and Exchange Commission.Recent Insider Transactions • Apr 28Independent Director recently bought US$83k worth of stockOn the 22nd of April, James Robinson bought around 40k shares on-market at roughly US$2.08 per share. This was the largest purchase by an insider in the last 3 months. This was the only on-market transaction from insiders over the last 12 months.Reported Earnings • Mar 31Full year 2020 earnings released: US$0.16 loss per share (vs US$0.19 loss in FY 2019)Full year 2020 results: Net loss: US$11.7m (loss narrowed 11% from FY 2019). Over the last 3 years on average, earnings per share has increased by 14% per year but the company’s share price has fallen by 18% per year, which means it is significantly lagging earnings.分析記事 • Mar 01What You Need To Know About Nymox Pharmaceutical Corporation's (NASDAQ:NYMX) Investor CompositionA look at the shareholders of Nymox Pharmaceutical Corporation ( NASDAQ:NYMX ) can tell us which group is most...Is New 90 Day High Low • Feb 11New 90-day high: US$3.10The company is up 52% from its price of US$2.04 on 12 November 2020. The American market is up 16% over the last 90 days, indicating the company outperformed over that time. It also outperformed the Biotechs industry, which is up 22% over the same period.Is New 90 Day High Low • Dec 19New 90-day high: US$2.83The company is up 16% from its price of US$2.43 on 18 September 2020. The American market is up 15% over the last 90 days, indicating the company outperformed over that time. However, it underperformed the Biotechs industry, which is up 17% over the same period.Is New 90 Day High Low • Dec 02New 90-day low: US$1.84The company is down 25% from its price of US$2.46 on 02 September 2020. The American market is up 5.0% over the last 90 days, indicating the company underperformed over that time. It also underperformed the Biotechs industry, which is up 13% over the same period.お知らせ • Nov 21Nymox Pharmaceutical Corporation, Annual General Meeting, Dec 21, 2020Nymox Pharmaceutical Corporation, Annual General Meeting, Dec 21, 2020, at 16:30 Eastern Daylight. Location: at the British Colonial Hilton, Nassau Bahamas, Number One Bay St Nassau Bahamas Agenda: To consider and receive the annual report of the directors, the financial statements of the corporation for the fiscal year ended December 31, 2019 and the auditors' report thereon; to consider to elect the directors of the corporation; to consider to appoint the auditors of the corporation and to authorize the board of directors to fix their remuneration; to ratify the acts of the members of the board of directors for the fiscal year ending 2019; and, up and to the date of this meeting; and to consider to transact such other matters as may properly be brought before the meeting, or any adjournment thereof.Is New 90 Day High Low • Oct 28New 90-day low: US$2.07The company is down 35% from its price of US$3.18 on 30 July 2020. The American market is up 6.0% over the last 90 days, indicating the company underperformed over that time. It also underperformed the Biotechs industry, which is down 3.0% over the same period.Is New 90 Day High Low • Oct 10New 90-day low: US$2.20The company is down 32% from its price of US$3.22 on 10 July 2020. The American market is up 9.0% over the last 90 days, indicating the company underperformed over that time. It also underperformed the Biotechs industry, which is flat over the same period.Is New 90 Day High Low • Sep 18New 90-day low: US$2.37The company is down 33% from its price of US$3.55 on 19 June 2020. The American market is up 10.0% over the last 90 days, indicating the company underperformed over that time. It also underperformed the Biotechs industry, which is down 2.0% over the same period.お知らせ • Aug 17Nymox Pharmaceutical Corporation has completed a Follow-on Equity Offering in the amount of $9 million.Nymox Pharmaceutical Corporation has completed a Follow-on Equity Offering in the amount of $9 million. Security Name: Common Stock Security Type: Common Stock Securities Offered: 3,600,000 Price\Range: $2.5 Discount Per Security: $0.175 Transaction Features: Registered Direct Offering株主還元NYMX.FUS BiotechsUS 市場7D-35.7%-1.7%-2.5%1Y-10.0%26.1%22.7%株主還元を見る業界別リターン: NYMX.F過去 1 年間で26.1 % の収益を上げたUS Biotechs業界を下回りました。リターン対市場: NYMX.Fは、過去 1 年間で22.7 % のリターンを上げたUS市場を下回りました。価格変動Is NYMX.F's price volatile compared to industry and market?NYMX.F volatilityNYMX.F Average Weekly Movement60.0%Biotechs Industry Average Movement10.9%Market Average Movement7.2%10% most volatile stocks in US Market16.6%10% least volatile stocks in US Market3.1%安定した株価: NYMX.Fの株価は、 US市場と比較して過去 3 か月間で変動しています。時間の経過による変動: NYMX.Fの 週次ボラティリティ は、過去 1 年間で41%から60%に増加しました。会社概要設立従業員CEO（最高経営責任者ウェブサイト1989n/aPaul Averbacknymox.comナイモックス・ファーマシューティカル・コーポレーション（Nymox Pharmaceutical Corporation）はバイオ医薬品会社で、カナダ、米国、欧州で高齢化社会に向けた製品の研究開発に従事している。同社の主要医薬品候補は、前立腺肥大症および低悪性度限局性前立腺癌、肝細胞癌の治療薬であるFexapotide Triflutate（NX-1207）である。また、喫煙状態を検出するNicAlert、受動喫煙暴露を検出するTobacAlertも提供している。さらに、アルツハイマー病治療薬の開発も行っている。同社は1989年に設立され、バハマのナッソーに本社を置いている。もっと見るNymox Pharmaceutical Corporation 基礎のまとめNymox Pharmaceutical の収益と売上を時価総額と比較するとどうか。NYMX.F 基礎統計学時価総額US$9.18m収益（TTM）-US$4.49m売上高(TTM)n/a0.0xP/Sレシオ-2.0xPER（株価収益率NYMX.F は割高か？公正価値と評価分析を参照収益と収入最新の決算報告書（TTM）に基づく主な収益性統計NYMX.F 損益計算書（TTM）収益US$0売上原価US$0売上総利益US$0その他の費用US$4.49m収益-US$4.49m直近の収益報告Dec 31, 2024次回決算日該当なし一株当たり利益（EPS）-0.044グロス・マージン0.00%純利益率0.00%有利子負債／自己資本比率-48.5%NYMX.F の長期的なパフォーマンスは？過去の実績と比較を見るView Valuation企業分析と財務データの現状データ最終更新日（UTC時間）企業分析2026/06/08 08:47終値2026/06/05 00:00収益2024/12/31年間収益2024/12/31データソース企業分析に使用したデータはS&P Global Market Intelligence LLC のものです。本レポートを作成するための分析モデルでは、以下のデータを使用しています。データは正規化されているため、ソースが利用可能になるまでに時間がかかる場合があります。パッケージデータタイムフレーム米国ソース例会社財務10年損益計算書キャッシュ・フロー計算書貸借対照表SECフォーム10-KSECフォーム10-Qアナリストのコンセンサス予想+プラス3年予想財務アナリストの目標株価アナリストリサーチレポートBlue Matrix市場価格30年株価配当、分割、措置ICEマーケットデータSECフォームS-1所有権10年トップ株主インサイダー取引SECフォーム4SECフォーム13Dマネジメント10年リーダーシップ・チーム取締役会SECフォーム10-KSECフォームDEF 14A主な進展10年会社からのお知らせSECフォーム8-K* 米国証券を対象とした例であり、非米国証券については、同等の規制書式および情報源を使用。特に断りのない限り、すべての財務データは1年ごとの期間に基づいていますが、四半期ごとに更新されます。これは、TTM（Trailing Twelve Month）またはLTM（Last Twelve Month）データとして知られています。詳細はこちら。分析モデルとスノーフレーク本レポートを生成するために使用した分析モデルの詳細は当社のGithubページでご覧いただけます。また、レポートの使用方法に関するガイドやYoutubeのチュートリアルも掲載しています。シンプリー・ウォールストリート分析モデルを設計・構築した世界トップクラスのチームについてご紹介します。業界およびセクターの指標私たちの業界とセクションの指標は、Simply Wall Stによって6時間ごとに計算されます。アナリスト筋Nymox Pharmaceutical Corporation 0 これらのアナリストのうち、弊社レポートのインプットとして使用した売上高または利益の予想を提出したのは、 。アナリストの投稿は一日中更新されます。0
お知らせ • May 02Nymox Pharmaceutical Corporation announced delayed 20-F filingOn 05/01/2025, Nymox Pharmaceutical Corporation announced that they will be unable to file their next 20-F by the deadline required by the SEC.
お知らせ • Mar 27Nymox Pharmaceutical Corporation Reports Victory in Bahamas Litigation Against Terminated Ex-Employees – Court Awards Costs and DamagesNymox Pharmaceutical Corporation reported that the Bahamas Supreme Court has issued a formal Order officially putting an end to the Bahamas litigation brought by terminated ex-employees. The Order also awards to Nymox its costs incurred in defending the ill-conceived lawsuit, as well as damages Nymox has suffered as a result of the litigation. The Court order states the following: The Interim Injunction Order is set aside; The damages caused to the Company shall be assessed by a Registrar and paid by the Claimants (the persons who filed the lawsuit); and The Claimants shall pay the Company’s net costs for the entire Action. This is the first of more than one action by and between the Company and Randall Lanham, (former General Counsel for Nymox), Chris Riley, (former short-term CFO), Richard Cutler (former external Counsel and member of Board), and their financial backers.
お知らせ • Sep 26Nymox Pharmaceutical Corporation Announces Submission of New Marketing Authorization Application Submission for NYMOZARFEX (TM) for BPHNymox Pharmaceutical Corporation announced that a new formal submission has been made by the company in the U.K. for Nymozarfex (TM) for the treatment of benign prostatic hyperplasia (BPH). The Marketing Authorization Application (MAA) was submitted to the U.K. Medicines & Healthcare products Regulatory Agency (MHRA). The new submission includes England, Wales, Scotland and Northern Ireland. The company will provide further information, including with respect to other submissions for Nymozarfex (TM), when the information becomes available.
お知らせ • Sep 08The Nasdaq Stock Market to Delist the Common Stock of Nymox PharmaceuticalThe Nasdaq Stock Market announced that it will delist the common stock of Nymox Pharmaceutical Corporation. Nymox Pharmaceutical Corporation’s securities were suspended on July 7, 2023, and have not traded on Nasdaq since that time.
お知らせ • Aug 03Nymox Pharmaceutical Corporation announced that it expects to receive $2 million in fundingNymox Pharmaceutical Corporation announced a private placement of 2,000,000 common shares at a price of $1.00 per share for gross proceeds of $2,000,000 on August 2, 2023. The company will also issue 500,000 warrants. The transaction included participation from James G. Robinson, an independent director of the company. The investment will close in the upcoming days after the customary formalities are completed.
お知らせ • Jul 26Nymox Pharmaceutical Corporation Reports Successful New NYMOZARFEX (TM) Long-Term Prostate Cancer Treatment Clinical Trial ResultsNymox Pharmaceutical Corporation announced important new long-term clinical trial results from the company's 146 patient NX03-0040 NYMOZARFEX (TM) U.S. study for low grade localized prostate cancer. New long-term follow-up data from the prospective randomized clinical trial of NYMOZARFEX (TM) for low grade early prostate cancer has indicated that there is strong statistically significant benefit from the treatment compared to controls when all available patient outcomes were included from 18 months to as long as up to >10 years after treatment. These additional 5 to 10-year data points add to the 5-year data that was published in the peer review World Journal of Urology in 2020 (World J Urol 38, 3101–3111 (2020). All clinical trial sites that were still open were contacted for follow-up data on the prostate cancer status of all available patients. A full effort was made to reach all possible subjects. The outcome comparisons showed greatly reduced percentages of subjects treated with NYMOZARFEX (TM) who had progressed by either cancer grade worsening or by prostate cancer surgery, radiotherapy, or chemotherapy; and which remained overall strongly statistically significant compared to the study's randomized controls (p<.01). This unique and successful study is the world's first and only long-term prospective randomized controlled study of an intraprostatic molecular injectable treatment for low-grade localized prostate cancer to have been accomplished. The new data represents the longest term data available from this major study. Study NX03-0040 was undertaken starting in 2012 at investigational sites across the U.S. with 146 men with the biopsy confirmed diagnosis of Grade Group1 prostate cancer. NYMOZARFEX (TM) was administered by a single painless injection directly into the prostate in a relatively simple procedure requiring several minutes or less in an office setting without sedation or anesthesia, and guided by routine ultrasound. NYMOZARFEX (TM) was injected into the area of the prostate where the cancer was previously detected prior to enrollment in NX03-0040. The patients were then biopsied after 6 weeks and then every 18 months, along with serial PSA measurements and long-term follow-up. All subjects with 18 months or more follow-up were compared with the inclusion of follow-up data from up to 10 years or more after a single injection of NYMOZARFEX (TM). For the patients where investigational sites were closed or where patients for unrelated reasons were no longer available, the last known status reports were included if they were 18 months or longer. For any subject with a worsening (increase) in grade of prostate cancer on biopsy; or with prostate cancer surgery, or radiotherapy or chemotherapy, they were included regardless of time after study treatment, and were counted in the calculation as treatment failures. The data shows that the number of patients with one focal injection of NYMOZARFEX (TM) 15 mg directed at the tumor had significantly less progression to more advanced cancer or to major cancer treatments, than the randomized control subjects followed in the study. Low grade localized prostate cancer (Gleason 3+3; T1c) is a very common treatment problem. The Nymox study reported involves patients with initially Gleason grade 3+3 or lower. These patients are found to have these tumors by biopsy which is usually instituted after finding abnormalities in PSA levels, and/or after abnormal digital rectal examination of the prostate, and/or after the patient has experienced lower urinary tract symptoms or other changes. Low grade localized prostate cancer represents a therapeutic challenge. Because of its slow growth and low initial level of malignancy, urologists and patients can be reluctant to proceed to invasive surgical treatments or radiotherapy due to the unpleasant and often permanent side effects these treatments cause in the genitourinary tract, such as sexual functional issues and/or urinary issues. Eventually if and when the tumor progresses, invasive surgical and/or radiotherapeutic procedures become necessary, with greater risk due to the progression. Occasionally the tumors become highly malignant after variable lengths of time. These risks cause understandable anxieties and distress and many men prefer to advance to invasive therapy before running these risks of higher grade cancers. It is widely acknowledged that a treatment like NYMOZARFEX (TM) that can destroy or ablate the low grade cancers of the prostate without the dreaded side effects and morbidities, would be an important benefit for these patients. Prostate cancer is the most commonly diagnosed cancer in men, other than skin cancer, and is the second leading cause of cancer death for men. Approximately 50% of prostate cancers are initially considered low risk. One of the major problems with the main current prostate treatments for localized prostate cancer (radical prostatectomy, external beam radiation, brachytherapy) is the relatively high incidence of serious sexual and other problems post- treatment. In 9 studies, NYMOZARFEX (TM) treatment has been shown to have a negligible significant adverse effect profile post-treatment and no significant adverse effects on sexual or other functions or testosterone levels. Leading urologists have long recognized the unmet need for prostate cancer treatments that can contribute to improved outcomes for their patients together with reduced side effects and stresses that may have significantly impact on quality of life. The goal of NYMOZARFEX (TM) injectable is to allow for an initial and less toxic treatment for low-risk prostate cancer patients, achieving the benefits of molecular ablation with minimal risk of side effects. For many patients, this treatment combined with surveillance would be extremely helpful for the unpleasant and persistent uncertainties, anxieties, and psychological/emotional burdens associated with only selecting active surveillance.
お知らせ • May 02Nymox Pharmaceutical Corporation announced delayed 20-F filingOn 05/01/2025, Nymox Pharmaceutical Corporation announced that they will be unable to file their next 20-F by the deadline required by the SEC.
お知らせ • Mar 27Nymox Pharmaceutical Corporation Reports Victory in Bahamas Litigation Against Terminated Ex-Employees – Court Awards Costs and DamagesNymox Pharmaceutical Corporation reported that the Bahamas Supreme Court has issued a formal Order officially putting an end to the Bahamas litigation brought by terminated ex-employees. The Order also awards to Nymox its costs incurred in defending the ill-conceived lawsuit, as well as damages Nymox has suffered as a result of the litigation. The Court order states the following: The Interim Injunction Order is set aside; The damages caused to the Company shall be assessed by a Registrar and paid by the Claimants (the persons who filed the lawsuit); and The Claimants shall pay the Company’s net costs for the entire Action. This is the first of more than one action by and between the Company and Randall Lanham, (former General Counsel for Nymox), Chris Riley, (former short-term CFO), Richard Cutler (former external Counsel and member of Board), and their financial backers.
お知らせ • Sep 26Nymox Pharmaceutical Corporation Announces Submission of New Marketing Authorization Application Submission for NYMOZARFEX (TM) for BPHNymox Pharmaceutical Corporation announced that a new formal submission has been made by the company in the U.K. for Nymozarfex (TM) for the treatment of benign prostatic hyperplasia (BPH). The Marketing Authorization Application (MAA) was submitted to the U.K. Medicines & Healthcare products Regulatory Agency (MHRA). The new submission includes England, Wales, Scotland and Northern Ireland. The company will provide further information, including with respect to other submissions for Nymozarfex (TM), when the information becomes available.
お知らせ • Sep 08The Nasdaq Stock Market to Delist the Common Stock of Nymox PharmaceuticalThe Nasdaq Stock Market announced that it will delist the common stock of Nymox Pharmaceutical Corporation. Nymox Pharmaceutical Corporation’s securities were suspended on July 7, 2023, and have not traded on Nasdaq since that time.
お知らせ • Aug 03Nymox Pharmaceutical Corporation announced that it expects to receive $2 million in fundingNymox Pharmaceutical Corporation announced a private placement of 2,000,000 common shares at a price of $1.00 per share for gross proceeds of $2,000,000 on August 2, 2023. The company will also issue 500,000 warrants. The transaction included participation from James G. Robinson, an independent director of the company. The investment will close in the upcoming days after the customary formalities are completed.
お知らせ • Jul 26Nymox Pharmaceutical Corporation Reports Successful New NYMOZARFEX (TM) Long-Term Prostate Cancer Treatment Clinical Trial ResultsNymox Pharmaceutical Corporation announced important new long-term clinical trial results from the company's 146 patient NX03-0040 NYMOZARFEX (TM) U.S. study for low grade localized prostate cancer. New long-term follow-up data from the prospective randomized clinical trial of NYMOZARFEX (TM) for low grade early prostate cancer has indicated that there is strong statistically significant benefit from the treatment compared to controls when all available patient outcomes were included from 18 months to as long as up to >10 years after treatment. These additional 5 to 10-year data points add to the 5-year data that was published in the peer review World Journal of Urology in 2020 (World J Urol 38, 3101–3111 (2020). All clinical trial sites that were still open were contacted for follow-up data on the prostate cancer status of all available patients. A full effort was made to reach all possible subjects. The outcome comparisons showed greatly reduced percentages of subjects treated with NYMOZARFEX (TM) who had progressed by either cancer grade worsening or by prostate cancer surgery, radiotherapy, or chemotherapy; and which remained overall strongly statistically significant compared to the study's randomized controls (p<.01). This unique and successful study is the world's first and only long-term prospective randomized controlled study of an intraprostatic molecular injectable treatment for low-grade localized prostate cancer to have been accomplished. The new data represents the longest term data available from this major study. Study NX03-0040 was undertaken starting in 2012 at investigational sites across the U.S. with 146 men with the biopsy confirmed diagnosis of Grade Group1 prostate cancer. NYMOZARFEX (TM) was administered by a single painless injection directly into the prostate in a relatively simple procedure requiring several minutes or less in an office setting without sedation or anesthesia, and guided by routine ultrasound. NYMOZARFEX (TM) was injected into the area of the prostate where the cancer was previously detected prior to enrollment in NX03-0040. The patients were then biopsied after 6 weeks and then every 18 months, along with serial PSA measurements and long-term follow-up. All subjects with 18 months or more follow-up were compared with the inclusion of follow-up data from up to 10 years or more after a single injection of NYMOZARFEX (TM). For the patients where investigational sites were closed or where patients for unrelated reasons were no longer available, the last known status reports were included if they were 18 months or longer. For any subject with a worsening (increase) in grade of prostate cancer on biopsy; or with prostate cancer surgery, or radiotherapy or chemotherapy, they were included regardless of time after study treatment, and were counted in the calculation as treatment failures. The data shows that the number of patients with one focal injection of NYMOZARFEX (TM) 15 mg directed at the tumor had significantly less progression to more advanced cancer or to major cancer treatments, than the randomized control subjects followed in the study. Low grade localized prostate cancer (Gleason 3+3; T1c) is a very common treatment problem. The Nymox study reported involves patients with initially Gleason grade 3+3 or lower. These patients are found to have these tumors by biopsy which is usually instituted after finding abnormalities in PSA levels, and/or after abnormal digital rectal examination of the prostate, and/or after the patient has experienced lower urinary tract symptoms or other changes. Low grade localized prostate cancer represents a therapeutic challenge. Because of its slow growth and low initial level of malignancy, urologists and patients can be reluctant to proceed to invasive surgical treatments or radiotherapy due to the unpleasant and often permanent side effects these treatments cause in the genitourinary tract, such as sexual functional issues and/or urinary issues. Eventually if and when the tumor progresses, invasive surgical and/or radiotherapeutic procedures become necessary, with greater risk due to the progression. Occasionally the tumors become highly malignant after variable lengths of time. These risks cause understandable anxieties and distress and many men prefer to advance to invasive therapy before running these risks of higher grade cancers. It is widely acknowledged that a treatment like NYMOZARFEX (TM) that can destroy or ablate the low grade cancers of the prostate without the dreaded side effects and morbidities, would be an important benefit for these patients. Prostate cancer is the most commonly diagnosed cancer in men, other than skin cancer, and is the second leading cause of cancer death for men. Approximately 50% of prostate cancers are initially considered low risk. One of the major problems with the main current prostate treatments for localized prostate cancer (radical prostatectomy, external beam radiation, brachytherapy) is the relatively high incidence of serious sexual and other problems post- treatment. In 9 studies, NYMOZARFEX (TM) treatment has been shown to have a negligible significant adverse effect profile post-treatment and no significant adverse effects on sexual or other functions or testosterone levels. Leading urologists have long recognized the unmet need for prostate cancer treatments that can contribute to improved outcomes for their patients together with reduced side effects and stresses that may have significantly impact on quality of life. The goal of NYMOZARFEX (TM) injectable is to allow for an initial and less toxic treatment for low-risk prostate cancer patients, achieving the benefits of molecular ablation with minimal risk of side effects. For many patients, this treatment combined with surveillance would be extremely helpful for the unpleasant and persistent uncertainties, anxieties, and psychological/emotional burdens associated with only selecting active surveillance.
お知らせ • Jul 13Nymox Pharmaceutical Corporation Appoints Patrick Doody as Vice President, General Counsel and Member of Board of DirectorsNymox Pharmaceutical Corporation announced the appointment of Patrick Doody as Vice President, General Counsel, and Member of Board of Directors. Mr. Doody joins Nymox from Pillsbury Winthrop Shaw Pittman LLP, where he was a partner in the Intellectual Property Group, and currently is Senior Counsel. Mr. Doody is a well-respected patent attorney with significant knowledge and experience in post-grant proceedings, patent infringement litigation, patent prosecution, licensing, opinions, and counseling. Mr. Doody has represented Nymox and its predecessor company in intellectual property matters for over 30 years, securing hundreds of issued patents for Nymox throughout the world. Mr. Doody is a former patent examiner, former in-house counsel for Union Carbide Corporation, former partner at Tier 1, AMLAW 100 firms, and also is an adjunct professor of patent law at the George Washington University School of Law. Mr. Doody obtained his BS degree in Chemical Engineering from Virginia Tech, and his law degree from the Scalia School of Law (formerly George Mason School of Law), has served in a number of leadership positions in various intellectual property associations, is ranked Band 2 by Chambers for Intellectual Property, and AV ranked by Martindale Hubbell. Much of Mr. Doodys legal career has involved counseling biotechnology, pharmaceutical, and chemical companies on all aspects of intellectual property law.
お知らせ • Jul 06Nymox Delisting from NASDAQNymox Pharmaceutical Corporation (the “Company”) received a Nasdaq Hearing Delist Decision, noting that Nymox has not regained the required $1.00 share price within the 6-month extension period granted by Nasdaq, and hence the Company's shares will be suspended from trading on NASDAQ at the open of business on July 7, 2023. Nymox shares will be moved to the OTC market. The mechanics of trading the stock remain the same, as do the Company's business fundamentals. Nymox is in the process of submitting applications for the approval to market the Company's first in class drug NYMOZARFEX to treat the symptoms of benign prostatic hyperplasia (BPH). BPH is one of the most common conditions affecting middle aged and elderly men throughout the world. BPH can be devastating to men who suffer from the condition. Current treatments are associated with numerous intolerable side effects including sexual problems, such as impotence and retrograde ejaculation. Medications for BPH have been associated with prostate cancer, depression, gynecomastia and other adverse effects. The majority of men stop taking the available medications due to these and other problems. Surgery is often needed for advanced BPH. Surgery is usually effective but it is not without risks, the discomforts of surgery, and BPH surgery has side effects such as permanent retrograde ejaculation for many patients. Nymozarfex was submitted to the Danish authorities in December 2022 and the application was accepted for review in early 2023 and is currently undergoing review. The Company announced that another submission was expected to be submitted for approval in another jurisdiction in the second quarter of 2023. It is expected to be submitted in the near future and the Company will provide the appropriate update when that occurs.
New Risk • Jul 01New major risk - Share price stabilityThe company's share price has been highly volatile over the past 3 months. It is more volatile than 90% of American stocks, typically moving 15% a week. This is considered a major risk. Share price volatility 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. It may also indicate 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. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-US$2.0m free cash flow). Share price has been highly volatile over the past 3 months (15% average weekly change). Negative equity (-US$1.8m). Revenue is less than US$1m. Minor Risk Market cap is less than US$100m (US$17.3m market cap).
お知らせ • Dec 06Nymox Pharmaceutical Corporation Announces New Marketing Submission for Nymozarfex for BPHNymox Pharmaceutical Corporation announced that a new formal submission has been made by the Company in Europe for Fexapotide Triflutate for the treatment of benign prostatic hyperplasia (BPH). The trademarked name for the product in the application is NYMOZARFEX (TM). The Marketing Authorization Application (MAA) was submitted to the Danish authorities. The Company will provide further information, including other expected submissions, when the information becomes available.
お知らせ • Nov 17Nymox Pharmaceutical Corporation, Annual General Meeting, Dec 12, 2022Nymox Pharmaceutical Corporation, Annual General Meeting, Dec 12, 2022, at 04:30 Eastern Daylight. Location: Margaritaville Resorts, Nassau Bahamas, Number Two Bay St Nasssau Bahamas Agenda: To receive the annual report of the directors, the financial statements of the corporation for the fiscal year ended December 31, 2021 and the auditors’ report thereon; to elect the directors of the corporation; to appoint the auditors of the corporation and to authorize the board of directors to fix their remuneration; to ratify the acts of the members of the board of directors for the fiscal year ending 2021; and, up and to the date of this meeting; to transact such other matters as may properly be brought before the meeting, or any adjournment thereof.
Board Change • Nov 16Insufficient new directorsNo new directors have joined the board in the last 3 years. The company's board is composed of: No new directors. 2 experienced directors. 3 highly experienced directors. Lead Independent Director Rich Cutler was the last director to join the board, commencing their role in 2015. The company’s insufficient board refreshment is considered a risk according to the Simply Wall St Risk Model.
Seeking Alpha • Sep 13Nymox gets FDA feedback on NDA resubmission for lead assetNymox Pharmaceutical (NASDAQ:NYMX), a biotech focused on drugs for the elderly, announced Tuesday that during the recent interactions, the FDA specified what additional information is required to resubmit a marketing application for its lead candidate Fexapotide. The company added that it is preparing the requested documentation in anticipation of the resubmission and looks forward to additional regulatory guidance from the FDA. In addition, NYMX announced plans to submit regulatory filings for Fexapotide in Q4 to seek European approval for the injection. Fexapotide Triflutate, also known as NX-1207, has undergone clinical studies for prostate-linked indications, including a Phase 3 trial for benign prostatic hyperplasia (BPH). However, in May, the company said that the FDA rejected to review the company’s marketing application for the drug in BPH.
分析記事 • Aug 17Is Nymox Pharmaceutical (NASDAQ:NYMX) In A Good Position To Deliver On Growth Plans?We can readily understand why investors are attracted to unprofitable companies. For example, although Amazon.com made...
お知らせ • Jul 15NYMOX Receives Deficiency Letter from NASDAQNymox Pharmaceutical Corporation (NASDAQ: NYMX) reported that on July 7, 2022 the Company received a deficiency letter from NASDAQ stating that the Company is no longer in compliance with Nasdaq Listing Rule 5550(a)(2). The Nasdaq letter states that the Company will be afforded 180 calendar days to regain compliance with the minimum bid price requirement. In order to regain compliance, the Company must have a closing bid price of $1.00 or more for a minimum of 10 consecutive business days. If at any time during this 180-day period the Company’s closing bid price meets or exceeds $1.00 for a minimum of 10 consecutive business days, Nasdaq will provide written confirmation of compliance and the matter will be closed. If the Company has not regained compliance by the expiration of the initial 180 calendar days, Nasdaq will then provide written notification to the Company that its ordinary shares are subject to delisting. At that time, the Company may appeal Nasdaq’s delisting determination to a Nasdaq Listing Qualifications Panel.
Seeking Alpha • Jul 14NYMOX stock down 7.2% after receiving non-compliance letter from NasdaqNymox Pharma (NASDAQ:NYMX) is down 7.2% after the company said it received a deficiency letter from Nasdaq stating that the company is no longer in compliance with Nasdaq. The company said it has 180 calendar days to regain compliance with the minimum bid price requirement. To regain compliance, the Company must have a closing bid price of $1.00 or more for a minimum of 10 consecutive business days.
お知らせ • Jul 09Nymox Pharmaceutical Corporation Announces Resignation of Erik Danielsen as Chief Financial OfficerNymox Pharmaceutical Corporation announced effective June 28, 2022, accepted the resignation of Erik Danielsen as Chief Financial Officer of the Company.
お知らせ • May 24NYMOX Receives RTF letter from FDANymox Pharmaceutical Corporation received a Refusal to File letter from FDA on May 20 at 2:48 pm EST, with regard to the Company's New Drug Application (“NDA”) for Fexapotide Triflutate. Nymox’s position is that clarifications remain to be resolved at a follow-up meeting and that some significant inconsistencies were involved. The letter referred to a new outstanding issue of longer-term safety data and indicated that Nymox needed to have longer-term safety data in its NDA. Longer-term full safety data (as long as 6 years after a single low dose non-systemic injection given one time only) was not requested by the FDA in any previous pre-NDA communications. The Company's position is that Fexapotide safety profile is superior to any other conventional BPH treatment. 2. Fexapotide is a local injection with no detectable drug outside of prostate in patients after treatment. For a single injection (ie, given only one time) low dose local administration treatment, typical human clinical safety data duration requirements for approvals are in the few months range or less. Animal testing requirements are generally 2 weeks. 3. The FDA agreed at the end of Phase 2 that for eventual approval one-year safety data after a single injection of fexapotide 2.5 mg was adequate for Phase 3 pivotal studies, for clinical safety duration requirements. In Nymox pivotal Phase 3 trials 0017 and 0018, this data was achieved, and 12-month full safety data was provided in the NDA. The FDA provided detailed safety requests at the fexapotide pre-NDA meeting, which categorically did not include a longer-term clinical safety data request for fexapotide. 5. In addition, the NDA does include even longer-term (2-3 years) full safety data for fexapotide from n=344 subjects in Phase 3 Studies NX02-0020 and NX02-0022. There is no evidence of any long-term adverse safety outcomes in the pivotal study data for fexapotide.
Board Change • Apr 27Insufficient new directorsNo new directors have joined the board in the last 3 years. The company's board is composed of: No new directors. 2 experienced directors. 3 highly experienced directors. Lead Independent Director Rich Cutler was the last director to join the board, commencing their role in 2015. The company’s insufficient board refreshment is considered a risk according to the Simply Wall St Risk Model.
お知らせ • Mar 05Nymox Pharmaceutical Corporation Announces Submission of New Drug Application to the FDA for Fexapotide TriflutateNymox Pharmaceutical Corporation announced that it has submitted the Company’s New Drug Application (NDA) to the FDA for Fexapotide Triflutate to seek marketing approval in the U.S. for Fexapotide Triflutate for the treatment of men with benign prostatic hyperplasia (BPH). The submission of the application does not involve any guarantees or forward looking statements regarding outcomes of the submission. The Company will continue to make updates on all material and required developments with the application, and in accordance with prior statements provided in the Company’s regular SEC filings. Nymox intends to submit applications in other major markets in the near term and will provide updates at the appropriate times in due course.
お知らせ • Jun 28+ 6 more updatesNymox Pharmaceutical Corporation(NasdaqCM:NYMX) dropped from Russell 3000E Value IndexNymox Pharmaceutical Corporation(NasdaqCM:NYMX) dropped from Russell 3000E Value Index
お知らせ • Apr 29Nymox Pharmaceutical Corporation announced that it expects to receive $7.999998 million in fundingNymox Pharmaceutical Corporation (NasdaqCM:NYMX) announced that it hsa entered in to definitive agreement for 3,669,724 shares at a price of $2.18 per share and warrants for the gross proceeds of $7,999,998.32? on April 28, 2021. Warrants issue in the transaction can be exercised in to 1,834,862 shares at a an exercise price of $2.50 per share and will expire five years from the date of issuance. The transaction is expected to close on or about April 30, 2021, subject to the satisfaction of customary closing conditions. The transaction is being made pursuant to the exemption from securities registration afforded by Section 4(a)(2) of the Securities Act of 1933, as amended, and Rule 506 of Regulation D as promulgated by the United States Securities and Exchange Commission.
Recent Insider Transactions • Apr 28Independent Director recently bought US$83k worth of stockOn the 22nd of April, James Robinson bought around 40k shares on-market at roughly US$2.08 per share. This was the largest purchase by an insider in the last 3 months. This was the only on-market transaction from insiders over the last 12 months.
Reported Earnings • Mar 31Full year 2020 earnings released: US$0.16 loss per share (vs US$0.19 loss in FY 2019)Full year 2020 results: Net loss: US$11.7m (loss narrowed 11% from FY 2019). Over the last 3 years on average, earnings per share has increased by 14% per year but the company’s share price has fallen by 18% per year, which means it is significantly lagging earnings.
分析記事 • Mar 01What You Need To Know About Nymox Pharmaceutical Corporation's (NASDAQ:NYMX) Investor CompositionA look at the shareholders of Nymox Pharmaceutical Corporation ( NASDAQ:NYMX ) can tell us which group is most...
Is New 90 Day High Low • Feb 11New 90-day high: US$3.10The company is up 52% from its price of US$2.04 on 12 November 2020. The American market is up 16% over the last 90 days, indicating the company outperformed over that time. It also outperformed the Biotechs industry, which is up 22% over the same period.
Is New 90 Day High Low • Dec 19New 90-day high: US$2.83The company is up 16% from its price of US$2.43 on 18 September 2020. The American market is up 15% over the last 90 days, indicating the company outperformed over that time. However, it underperformed the Biotechs industry, which is up 17% over the same period.
Is New 90 Day High Low • Dec 02New 90-day low: US$1.84The company is down 25% from its price of US$2.46 on 02 September 2020. The American market is up 5.0% over the last 90 days, indicating the company underperformed over that time. It also underperformed the Biotechs industry, which is up 13% over the same period.
お知らせ • Nov 21Nymox Pharmaceutical Corporation, Annual General Meeting, Dec 21, 2020Nymox Pharmaceutical Corporation, Annual General Meeting, Dec 21, 2020, at 16:30 Eastern Daylight. Location: at the British Colonial Hilton, Nassau Bahamas, Number One Bay St Nassau Bahamas Agenda: To consider and receive the annual report of the directors, the financial statements of the corporation for the fiscal year ended December 31, 2019 and the auditors' report thereon; to consider to elect the directors of the corporation; to consider to appoint the auditors of the corporation and to authorize the board of directors to fix their remuneration; to ratify the acts of the members of the board of directors for the fiscal year ending 2019; and, up and to the date of this meeting; and to consider to transact such other matters as may properly be brought before the meeting, or any adjournment thereof.
Is New 90 Day High Low • Oct 28New 90-day low: US$2.07The company is down 35% from its price of US$3.18 on 30 July 2020. The American market is up 6.0% over the last 90 days, indicating the company underperformed over that time. It also underperformed the Biotechs industry, which is down 3.0% over the same period.
Is New 90 Day High Low • Oct 10New 90-day low: US$2.20The company is down 32% from its price of US$3.22 on 10 July 2020. The American market is up 9.0% over the last 90 days, indicating the company underperformed over that time. It also underperformed the Biotechs industry, which is flat over the same period.
Is New 90 Day High Low • Sep 18New 90-day low: US$2.37The company is down 33% from its price of US$3.55 on 19 June 2020. The American market is up 10.0% over the last 90 days, indicating the company underperformed over that time. It also underperformed the Biotechs industry, which is down 2.0% over the same period.
お知らせ • Aug 17Nymox Pharmaceutical Corporation has completed a Follow-on Equity Offering in the amount of $9 million.Nymox Pharmaceutical Corporation has completed a Follow-on Equity Offering in the amount of $9 million. Security Name: Common Stock Security Type: Common Stock Securities Offered: 3,600,000 Price\Range: $2.5 Discount Per Security: $0.175 Transaction Features: Registered Direct Offering
