Announcement • Aug 04
Oramed Pharmaceuticals Inc., Annual General Meeting, Sep 15, 2026 Oramed Pharmaceuticals Inc., Annual General Meeting, Sep 15, 2026. Location: 20 mamila, avenue, 3rd floor, jerusalem Israel Announcement • May 17
Oramed Pharmaceuticals Inc. announced delayed 10-Q filing On 05/15/2026, Oramed Pharmaceuticals Inc. announced that they will be unable to file their next 10-Q by the deadline required by the SEC. Announcement • Mar 26
Lifeward Ltd. (NasdaqCM:LFWD) completed the acquisition of Oratech Pharma, Inc. from Oramed Pharmaceuticals Inc. (NasdaqCM:ORMP). Lifeward Ltd. (NasdaqCM:LFWD) entered into a share purchase agreement to acquire Oratech Pharma, Inc. from Oramed Pharmaceuticals Inc. (NasdaqCM:ORMP) on January 12, 2026. At closing, the Company will issue ordinary shares and pre-funded warrants to Oramed Pharmaceuticals, Inc. in an amount representing 49.99% of the Company’s fully diluted equity capitalization, subject to certain adjustments and ownership limitations. The number of ordinary shares issued at closing is capped at 45% of Lifeward’s outstanding ordinary shares, with the balance issued in the form of pre-funded warrants. Approximately 5% of the equity consideration will be held back in the form of pre-funded warrants for indemnification purposes and released after 12 months, subject to claims. In addition, the Company will issue transaction warrants to purchase ordinary shares, with the number of warrants determined by dividing Lifeward’s net cash at closing by an exercise price of $0.45 per share. As further consideration, Lifeward agreed to make contingent quarterly revenue-sharing payments equal to 4% of net revenue from sales of ReWalk Personal Exoskeleton products and related warranties.
The transaction is subject to approval by regulatory board / committee, approval of offer by acquirer shareholders, registration statement effectiveness (S-4 / F-4), lock-up agreement and listing / approval of new shares on stock exchange. The transaction has received unanimous approval from Lifeward’s board of directors. The transaction is contingent upon closing conditions. As of March 12, 2026, Lifeward Ltd. shareholders approved the transaction.
Rachael M. Bushey and Jennifer Porter of Goodwin Procter LLP acted as legal advisor for Lifeward Ltd. Aaron M. Lampert and Ephraim P. Friedman of Goldfarb Seligman & Co. acted as legal advisor for Lifeward Ltd. Rick A. Werner, Alla Digilova, and Simin Sun of Haynes and Boone, LLP acted as legal advisor for Oramed Pharmaceuticals Inc.
Lifeward Ltd. (NasdaqCM:LFWD) completed the acquisition of Oratech Pharma, Inc. from Oramed Pharmaceuticals Inc. (NasdaqCM:ORMP) on March 25, 2026. At closing, Lifeward issued an aggregate 2,256,476 shares of its ordinary shares and pre-funded warrants. Lifeward also issued 1,296,296 warrants to purchase Oratech Pharma's ordinary shares. Announcement • Jan 08
Oramed Pharmaceuticals Inc. Approves Cash Dividend Payable on January 26, 2026 Oramed Pharmaceuticals Inc.'s Board of Directors approved a cash dividend payment of $0.25 per share. The dividend will have an ex-dividend date of January 16, 2026, with disbursement scheduled for January 26, 2026. The dividend is expected to result in an aggregate distribution of approximately $10.5 million based on the current number of shares outstanding. The dividend will be funded with surplus capital. Announcement • Jan 01
Oramed Pharmaceuticals Inc. Announces Resignation of Leonard Sank from the Board, Effective as of January 1, 2026 On December 31, 2025, the board of directors (the “Board”) of Oramed Pharmaceuticals Inc. (the “Company”) received notice of Leonard Sank’s intention to resign from the Board, effective as of January 1, 2026. Mr. Sank’s resignation did not result from any disagreement with the Company on any matter relating to the Company’s operations, policies or practices. Mr. Sank served 18 years at the Company. Announcement • Nov 18
Oramed Pharmaceuticals Inc. Declares Dividend Distribution of Common Stock, Payable on November 27, 2025 The Board of Directors of Oramed Pharmaceuticals Inc. announced that it has unanimously adopted a Rights Agreement, dated November 17, 2025 (the "Rights Plan"), by and between the Company and Continental Stock Transfer & Trust Company, as rights agent, and declared a dividend of one common stock purchase right (a "Right") on each outstanding share of its common stock, par value $0.012 per share (the "Common Stock"), of the Company. The dividend distribution will be payable on November 27, 2025, to stockholders of record as of the close of business on November 27, 2025. Announcement • Jul 17
Oramed Pharmaceuticals Inc., Annual General Meeting, Aug 19, 2025 Oramed Pharmaceuticals Inc., Annual General Meeting, Aug 19, 2025. Location: proskauer rose llp, one boca place, 2255 glades road, suite 421 atrium, fl 33431-7360, boca raton United States New Risk • Aug 16
New major risk - Earnings quality The company has a high level of non-cash earnings. Accrual ratio: 188% This is considered a major risk. Non-cash earnings can arise from many different things. However, if a company consistently has a high level of non-cash earnings, it may be a sign that they are recognizing revenue from customers before the full value of the sales are received as cash or they are not depreciating the value of their assets appropriately. These are practices that inflate earnings, while not providing a similar increase to cash flows. Companies in some select industries naturally have a high level of non-cash earnings and it is not a major concern. However, in the worst case scenario it can be an early sign of performance manipulation by management. Currently, the following risks have been identified for the company: Major Risks Earnings are forecast to decline by an average of 198% per year for the foreseeable future. High level of non-cash earnings (188% accrual ratio). Revenue is less than US$1m. Minor Risks Share price has been volatile over the past 3 months (10% average weekly change). Market cap is less than US$100m (€86.8m market cap, or US$95.5m). Valuation Update With 7 Day Price Move • Aug 05
Investor sentiment deteriorates as stock falls 15% After last week's 15% share price decline to €1.98, the stock trades at a trailing P/E ratio of 8.6x. Average forward P/E is 16x in the Pharmaceuticals industry in Germany. Total loss to shareholders of 89% over the past three years. New Risk • Jul 31
New minor risk - Market cap size The company's market capitalization is less than US$100m. Market cap: €91.2m (US$98.7m) This is considered a minor risk. Companies with a small market capitalization are most likely businesses that have not yet released a product to market or are simply a very small company without a wide reach. Either way, risk is elevated with these companies because there is a chance the product may not come to fruition or the company's addressable market or demand may not be as large as expected. In addition, if the company's size is the main factor, it is less likely to have many investors and analysts following it and scrutinizing its performance and outlook. Currently, the following risks have been identified for the company: Major Risks Earnings are forecast to decline by an average of 169% per year for the foreseeable future. Revenue is less than US$1m (US$674k revenue). Minor Risks Share price has been volatile over the past 3 months (9.1% average weekly change). Large one-off items impacting financial results. Market cap is less than US$100m (€91.2m market cap, or US$98.7m). Valuation Update With 7 Day Price Move • Jun 28
Investor sentiment improves as stock rises 22% After last week's 22% share price gain to €2.44, the stock trades at a trailing P/E ratio of 10x. Average forward P/E is 18x in the Pharmaceuticals industry in Germany. Total loss to shareholders of 77% over the past three years. Announcement • Jun 27
Oramed Pharmaceuticals Inc. (NasdaqCM:ORMP) announces an Equity Buyback for $20 million worth of its shares. Oramed Pharmaceuticals Inc. (NasdaqCM:ORMP) announces a share repurchase program. Under the program, the company will repurchase up to $20 million worth of its shares. The program will expired in 12 months. Announcement • Jun 22
Oramed Pharmaceuticals Inc., Annual General Meeting, Aug 01, 2024 Oramed Pharmaceuticals Inc., Annual General Meeting, Aug 01, 2024. Location: 20 mamilla avenue, israel 9414904, jerusalem Israel Valuation Update With 7 Day Price Move • Jun 12
Investor sentiment improves as stock rises 17% After last week's 17% share price gain to €2.25, the stock trades at a trailing P/E ratio of 9.1x. Average forward P/E is 18x in the Pharmaceuticals industry in Germany. Total loss to shareholders of 80% over the past three years. New Risk • May 20
New major risk - Revenue and earnings growth Earnings are forecast to decline by an average of 95% per year for the foreseeable future. This is considered a major risk. Ultimately, shareholders want to see a good return on their investment and that generally comes from sharing in the company's profits. If profits are expected to decline, then in most cases the share price will decline over time as well. In addition, if the company pays dividends it will also likely need to reduce or cut them, striking a dual blow to total shareholder returns. Currently, the following risks have been identified for the company: Major Risks Earnings are forecast to decline by an average of 95% per year for the foreseeable future. Revenue is less than US$1m (US$674k revenue). Minor Risks Large one-off items impacting financial results. Market cap is less than US$100m (€86.0m market cap, or US$93.4m). Reported Earnings • May 13
First quarter 2024 earnings released: EPS: US$0.038 (vs US$0.085 loss in 1Q 2023) First quarter 2024 results: EPS: US$0.038 (up from US$0.085 loss in 1Q 2023). Net income: US$1.54m (up US$4.93m from 1Q 2023). Over the last 3 years on average, earnings per share has increased by 46% per year but the company’s share price has fallen by 37% per year, which means it is significantly lagging earnings. New Risk • Apr 16
New minor risk - Market cap size The company's market capitalization is less than US$100m. Market cap: €92.3m (US$98.1m) This is considered a minor risk. Companies with a small market capitalization are most likely businesses that have not yet released a product to market or are simply a very small company without a wide reach. Either way, risk is elevated with these companies because there is a chance the product may not come to fruition or the company's addressable market or demand may not be as large as expected. In addition, if the company's size is the main factor, it is less likely to have many investors and analysts following it and scrutinizing its performance and outlook. Currently, the following risks have been identified for the company: Minor Risks Share price has been volatile over the past 3 months (9.6% average weekly change). Large one-off items impacting financial results. Revenue is less than US$5m (US$1.3m revenue). Market cap is less than US$100m (€92.3m market cap, or US$98.1m). Announcement • Mar 19
Oramed Pharmaceuticals Inc. has filed a Follow-on Equity Offering in the amount of $75 million. Oramed Pharmaceuticals Inc. has filed a Follow-on Equity Offering in the amount of $75 million.
Security Name: COMMON STOCK
Security Type: Common Stock
Transaction Features: At the Market Offering Reported Earnings • Mar 07
Full year 2023 earnings released: EPS: US$0.14 (vs US$0.94 loss in FY 2022) Full year 2023 results: EPS: US$0.14 (up from US$0.94 loss in FY 2022). Net income: US$5.53m (up US$42.1m from FY 2022). Over the last 3 years on average, earnings per share has increased by 22% per year but the company’s share price has fallen by 24% per year, which means it is significantly lagging earnings. Board Change • Jan 23
Insufficient new directors No new directors have joined the board in the last 3 years. The company's board is composed of: No new directors. 6 experienced directors. 5 highly experienced directors. Member of Scientific Advisory Board Jay Skyler was the last director to join the board, commencing their role in 2020. The following issues are considered to be risks according to the Simply Wall St Risk Model: Insufficient board refreshment. Announcement • Dec 19
Oramed Pharmaceuticals Inc. Appoints Daniel Aghion as Director, Effective January 1, 2024 On December 18, 2023, Oramed Pharmaceuticals Inc. (Company) increased the size of its Board of Directors by one and appointed Dr. Daniel Aghion to serve as a director to fill the resulting vacancy, effective as of January 1, 2024. The Board has not yet taken action to appoint Dr. Aghion to any committees of the Board. Dr. Daniel Aghion, age 42, is a neurosurgeon at Memorial Neuroscience Institute in Florida since 2016, where he treats patients with a wide array of spine disorders, including severe degenerative spine diseases, spine trauma, cancer in the spine, spine tumors, peripheral nerve surgery and more. Dr. Aghion holds a Bachelor's of Science degree from the University of Michigan and an MD from the Sackler School of Medicine at Tel Aviv University. He completed his residency at Rhode Island Hospital in 2015, and a complex spine fellowship at Johns Hopkins University in Baltimore in 2016. Reported Earnings • Nov 12
Third quarter 2023 earnings released: US$0.08 loss per share (vs US$0.18 loss in 3Q 2022) Third quarter 2023 results: US$0.08 loss per share (improved from US$0.18 loss in 3Q 2022). Net loss: US$3.22m (loss narrowed 54% from 3Q 2022). Revenue is expected to decline by 70% p.a. on average during the next 2 years, while revenues in the Pharmaceuticals industry in Germany are expected to grow by 3.6%. Over the last 3 years on average, earnings per share has remained flat but the company’s share price has fallen by 8% per year, which means it is significantly lagging earnings. New Risk • Oct 13
New major risk - Share price stability The company's share price has been highly volatile over the past 3 months. It is more volatile than 90% of German stocks, typically moving 8.5% 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 Share price has been highly volatile over the past 3 months (8.5% average weekly change). Earnings are forecast to decline by an average of 21% per year for the foreseeable future. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$47m net loss in 3 years). Shareholders have been diluted in the past year (3.7% increase in shares outstanding). Revenue is less than US$5m (US$2.7m revenue). Market cap is less than US$100m (€81.7m market cap, or US$85.8m). New Risk • Oct 05
New minor risk - Market cap size The company's market capitalization is less than US$100m. Market cap: €88.4m (US$93.0m) This is considered a minor risk. Companies with a small market capitalization are most likely businesses that have not yet released a product to market or are simply a very small company without a wide reach. Either way, risk is elevated with these companies because there is a chance the product may not come to fruition or the company's addressable market or demand may not be as large as expected. In addition, if the company's size is the main factor, it is less likely to have many investors and analysts following it and scrutinizing its performance and outlook. Currently, the following risks have been identified for the company: Major Risk Earnings are forecast to decline by an average of 21% per year for the foreseeable future. Minor Risks Currently unprofitable and not forecast to become profitable over next 3 years (US$47m net loss in 3 years). Share price has been volatile over the past 3 months (8.0% average weekly change). Shareholders have been diluted in the past year (3.7% increase in shares outstanding). Revenue is less than US$5m (US$2.7m revenue). Market cap is less than US$100m (€88.4m market cap, or US$93.0m). Reported Earnings • Aug 11
Second quarter 2023 earnings released: US$0.03 loss per share (vs US$0.27 loss in 2Q 2022) Second quarter 2023 results: US$0.03 loss per share (improved from US$0.27 loss in 2Q 2022). Net loss: US$1.19m (loss narrowed 89% from 2Q 2022). Revenue is expected to decline by 84% p.a. on average during the next 3 years, while revenues in the Pharmaceuticals industry in Germany are expected to grow by 3.1%. Over the last 3 years on average, earnings per share has fallen by 9% per year but the company’s share price has only fallen by 2% per year, which means it has not declined as severely as earnings. Announcement • Aug 09
Oramed Pharmaceuticals Inc. (NasdaqCM:ORMP) entered into a Stalking Horse Stock Purchase Term Sheet to acquire a 40.17% stake in Scilex Holding Company (NasdaqCM:SCLX) from Sorrento Therapeutics, Inc. (OTCPK:SRNE.Q) for approximately $110 million. Oramed Pharmaceuticals Inc. (NasdaqCM:ORMP) entered into a Stalking Horse Stock Purchase Term Sheet to acquire a 40.17% stake in Scilex Holding Company (NasdaqCM:SCLX) from Sorrento Therapeutics, Inc. (OTCPK:SRNE.Q) for approximately $110 million on August 4, 2023. Oramed Pharmaceuticals Inc. entered into a Stalking Horse Agreement to acquire a 40.17% stake in Scilex Holding Company from Sorrento Therapeutics, Inc. on August 8, 2023. Oramed to purchase 59,726,737 shares of common stock of Scilex and 29,057,096 shares of Series A preferred stock of Scilex under the transaction. As a part of consideration, Oramed will provide a non-amortizing super-priority debtor-in-possession term loan financing facility in an aggregate principal amount of $100 million (the “Replacement DIP Facility”) and remaining consideration in cash. Oramed Pharmaceuticals Inc. will receive a a break-up fee in the amount of $3,412,500, in case of termmination. Oramed will be capitalized with sufficient debt and equity capital to fund the cash portion of the Purchase Price. Term Sheet is subject to a final definitive documentation to be negotiated in good faith between the parties, uthorization and approval by the United States Bankruptcy Court for the Southern District of Texas,all HSR filing and waiting periods applicable to the Sale shall have expired or been terminated, all other governmental and regulatory approvals, if any, shall have been obtained, parties shall have entered into a new Registration Rights Agreement, approval of board of directors of Scilex and satisfaction or waiver of the other Closing Conditions. The proposed transaction will not be subject to a financing contingency.
The stalking horse agreement with Oramed is subject to an auction and the submission of higher or otherwise better offers. Any parties interested in bidding for the Scilex Stock should email Sorrento's investment banker (Moelis & Company LLC) as soon as possible to indicate their interest and discuss required bid materials. To the extent Sorrento receives any qualified bids that are higher or otherwise better than Oramed's bid by August 11, 2023, at 5:00 p.m. (ET), Sorrento will hold an auction for the Scilex Stock on August 14, 2023. The U.S. Bankruptcy Court for the Southern District of Texas (the "Bankruptcy Court") approved the transaction on August 8, 2023. Transaction is expected to be completed by or before September 15, 2023.
Latham & Watkins LLP and Jackson Walker LLP are serving as legal counsel to Sorrento. M3 Partners is serving as restructuring advisor. Moelis & Company LLC is serving as financial advisor and investment banker. H.C. Wainwright & Co. acted as financial and capital markets advisor to Oramed. Announcement • Jul 12
Oramed Pharmaceuticals Inc., Annual General Meeting, Jul 13, 2023 Oramed Pharmaceuticals Inc., Annual General Meeting, Jul 13, 2023, at 16:00 Israel Standard Time. Location: 20 Mamilla Avenue Jerusalem Israel Agenda: To consider and re-elect six directors of the Company to hold office until next annual meeting of stockholders and until their respective successors shall be elected and qualified or until their earlier resignation or removal; to consider and ratify the appointment of Kesselman & Kesselman, certified public accountants in Israel, a member of PricewaterhouseCoopers International Limited as the independent registered public accounting firm of the Company for the 2023 fiscal year; and to transact any other business as may properly come before the Annual Meeting or any adjournments thereof. Reported Earnings • May 13
First quarter 2023 earnings released: US$0.085 loss per share (vs US$0.27 loss in 1Q 2022) First quarter 2023 results: US$0.085 loss per share (improved from US$0.27 loss in 1Q 2022). Net loss: US$3.40m (loss narrowed 67% from 1Q 2022). Revenue is forecast to grow 24% p.a. on average during the next 3 years, compared to a 3.8% growth forecast for the Pharmaceuticals industry in Germany. Over the last 3 years on average, earnings per share has fallen by 17% per year but the company’s share price has only fallen by 2% per year, which means it has not declined as severely as earnings. Recent Insider Transactions • Mar 21
President recently bought €188k worth of stock On the 14th of March, Nadav Kidron bought around 100k shares on-market at roughly €1.88 per share. This transaction amounted to 11% of their direct individual holding at the time of the trade. This was the largest purchase by an insider in the last 3 months. Nadav has been a buyer over the last 12 months, purchasing a net total of €237k worth in shares. Recent Insider Transactions • Mar 16
Independent Director recently bought €132k worth of stock On the 14th of March, Yadin Rozov bought around 70k shares on-market at roughly €1.89 per share. This transaction increased Yadin's direct individual holding by 4x at the time of the trade. This was the largest purchase by an insider in the last 3 months. Insiders have collectively bought €47k more in shares than they have sold in the last 12 months. Reported Earnings • Mar 08
Full year 2022 earnings released: US$0.94 loss per share (vs US$0.94 loss in FY 2021) Full year 2022 results: US$0.94 loss per share. Net loss: US$36.6m (loss widened 4.4% from FY 2021). Revenue is forecast to grow 26% p.a. on average during the next 3 years, compared to a 3.4% growth forecast for the Pharmaceuticals industry in Germany. Announcement • Jan 12
Oramed Pharmaceuticals Inc. Announces Top-Line Results from Phase 3 Trial of ORMD-0801 for the Treatment of Type 2 Diabetes Oramed Pharmaceuticals Inc. announced top-line results from its Phase 3 randomized, double-blind, placebo-controlled, multicenter clinical trial (ORA-D-013-1) comparing the efficacy of ORMD-0801 to placebo in patients with Type 2 Diabetes (T2D) at 26 weeks. ORA-D-013-1 enrolled 710 patients with T2D and inadequate glycemic control on two or three oral glucose-lowering agents. The ORA-D-013-1 trial did not meet its primary endpoint, which compared the efficacy of ORMD-0801 to placebo in improving glycemic control as assessed by the mean change from baseline in A1C at 26 weeks. The trial also did not meet its secondary endpoint, which assessed the mean change from baseline in fasting plasma glucose at 26 weeks. There were no serious drug-related adverse events. Therefore, Oramed expects to discontinue its oral insulin clinical activities for T2D. Additional Information About the ORA-D-013-1 Phase 3 Clinical Trial: In the ORA-D-013-1 trial, patients were randomized 2:2:1:1 into four groups: 8 mg dosed once-daily; 8 mg dosed twice-daily; placebo dosed once-daily; and placebo dosed twice-daily. Patients completed an initial 21-day Screening Period, followed by a 26-week Double-Blind Treatment Period. Announcement • Jan 05
Oramed Pharmaceuticals Inc. Granted U.S. Combination Therapy Patent for Oral Glp-1 & Insulin for the Treatment of Diabetes Oramed Pharmaceuticals Inc. announced that the United States Patent and Trademark Office has granted the Company a patent titled "Methods and Compositions for Treating Diabetes." The patent serves as an extension to a patent previously granted in May 2022 and addresses methods and compositions for treating diabetes mellitus through oral pharmaceutical compositions comprising insulin in combination with Glucagon-like Peptide 1 (GLP-1). Announcement • Nov 20
Oramed Announces Additional Positive Safety and Efficacy Data from Its Phase 2 Clinical Trial of ORMD-0801 for NASH Oramed Pharmaceuticals Inc. announced additional positive data from its Phase 2 double-blind, fully randomized, placebo-controlled, multicenter clinical trial (ORA-D-N02) to assess the safety and efficacy of its oral insulin candidate (ORMD-0801), to reduce liver fat content in Type 2 Diabetes patients with non-alcoholic steatohepatitis ("NASH"). The presentation of this new data, including a discussion by key opinion leaders, was featured in a webinar with a replay available on Oramed's website under Events and Presentations. As previously announced, the Phase 2 trial enrolled 32 patients (with 30 patients completing) over a treatment period of 12-weeks. The trial demonstrated that ORMD-0801 was safe and well tolerated at 8 mg twice daily dosing, meeting the primary endpoint of no difference in adverse events for ORMD-0801 compared to placebo. The trial also evaluated the effectiveness of ORMD-0801 in reducing liver fat content over the 12-week treatment period by observing several independent measures. These measurements included MR PDFF (%) as measured by MRI, Steatosis and Fibrosis as measured by Fibroscan, Lipids and HbA1c. All the measurements showed a consistent clinically meaningful trend in favor of ORMD-0801. Safety Data Summary: Primary objective of safety met with no serious adverse events and no difference in the incidence rate of adverse events between ORMD-0801 and placebo. Efficacy Data Summary Overall, the Phase 2 trial achieved the proof of concept that ORMD-0801 may be a potential candidate for the reduction in liver fat and stiffness and lipids in patients with T2D and NASH. condaryry objective of reducing liver fat content in patients with NASH anT2D (Percent Change from Baseleline to Week 12 in MR PDFF (%): Whole Liver showed a placebo adjusted mean decrease of 0.96 with a placebo adjusted median decrease of 6.0 for ORMD-0801. Exploratory objective of median change from baseline in Fibroscan fibrosis levels:- Median Change from Baseline to Week 12 in Fibrosis Median (kPa) showed a placebo adjusted median decrease of 1.1 for ORMD-0801. - Median change from Baseline to Week 12 in Steatosis Median (dB/m) showed a placebo adjusted median decrease of 29 for ORMD-0801. Exploratory objective of change from baseline in Lipid levels:- Mean Change from Baseline to Week 12 in Total Cholesterol (mmol/L) showed a placebo adjusted mean decrease of 0.40 for ORMD-0801.- Results were similar for LDL, HDL and Triglycerides. Reported Earnings • Nov 16
Third quarter 2022 earnings released: US$0.18 loss per share (vs US$0.21 loss in 3Q 2021) Third quarter 2022 results: US$0.18 loss per share. Net loss: US$7.06m (loss widened 3.0% from 3Q 2021). Revenue is forecast to grow 73% p.a. on average during the next 3 years, compared to a 3.9% growth forecast for the Pharmaceuticals industry in Germany. Board Change • Nov 16
High number of new and inexperienced directors There are 5 new directors who have joined the board in the last 3 years. The company's board is composed of: 5 new directors. 2 experienced directors. 5 highly experienced directors. Chief Scientific Officer & Director Miriam Kidron is the most experienced director on the board, commencing their role in 2006. The following issues are considered to be risks according to the Simply Wall St Risk Model: Lack of board continuity. Lack of experienced directors. Reported Earnings • Nov 12
Third quarter 2022 earnings released: US$0.18 loss per share (vs US$0.21 loss in 3Q 2021) Third quarter 2022 results: US$0.18 loss per share. Net loss: US$7.06m (loss widened 3.0% from 3Q 2021). Revenue is forecast to grow 86% p.a. on average during the next 3 years, compared to a 4.1% growth forecast for the Pharmaceuticals industry in Germany. Announcement • Sep 14
Oramed Pharmaceuticals Inc. Reports Positive Top-Line Results from Phase 2 Nash Trial with its ORMD-0801, Oral Insulin Candidate Oramed Pharmaceuticals Inc. announced positive Phase 2 results from its double-blind, fully randomized, placebo-controlled, multicenter trial to assess the safety and efficacy of its oral insulin candidate (ORMD-0801), to reduce liver fat content in Type 2 Diabetes patients with non-alcoholic steatohepatitis. The 12-week trial enrolled 32 patients (with 30 patients completing) and demonstrated that ORMD-0801 was safe and well tolerated at 8 mg twice daily dosing, meeting the primary endpoint of no difference in adverse events for ORMD-0801 compared to placebo. The trial also evaluated the effectiveness of ORMD-0801 in reducing liver fat content over the 12-week treatment period by observing several independent measures. These measurements included MR PDFF(%) as measured by MRI, Steatosis and Fibrosis as measured by Fibroscan, Lipids and HbA1c. All the measurements showed a consistent clinically meaningful trend in favor of ORMD-0801. Reported Earnings • Aug 12
Second quarter 2022 earnings released: US$0.27 loss per share (vs US$0.17 loss in 2Q 2021) Second quarter 2022 results: US$0.27 loss per share (down from US$0.17 loss in 2Q 2021). Net loss: US$10.5m (loss widened 102% from 2Q 2021). Over the next year, revenue is forecast to grow 6.4%, compared to a 6.4% growth forecast for the industry in Germany. Over the last 3 years on average, earnings per share has fallen by 10% per year but the company’s share price has increased by 45% per year, which means it is well ahead of earnings. Announcement • Jul 27
Oramed Reaches 50% Enrollment in Its Second Phase 3 Oral Insulin Trial Oramed Pharmaceuticals Inc. announced that it has enrolled and randomized over 50% of the planned 450 patients for its international multicenter Phase 3 ORA-D-013-2 trial of its oral insulin capsule, ORMD-0801, for the treatment of type 2 diabetes (T2D). ORA-D-013-2 is the second of Oramed's two Phase 3 trials being conducted under U.S. Food and Drug Administration (FDA) Investigational New Drug Application (IND) to treat T2D patients who have inadequate glycemic control over a period of 6 to 12 months. The ORA-D-013-2 trial is recruiting 450 T2D patients with inadequate glycemic control who are managing their condition with either diet alone or with diet and metformin monotherapy. The double-blind trial will randomize patients 1:1 into two cohorts dosed with 8 mg of ORMD-0801 at night or placebo at night. The primary endpoint of the trial is to compare the efficacy of ORMD-0801 to placebo in improving glycemic control as assessed by A1c over a 26-week treatment period, with a secondary endpoint of comparing ORMD-0801 to placebo in maintaining glycemic control over a 52-week treatment period. Board Change • Jul 15
High number of new and inexperienced directors There are 5 new directors who have joined the board in the last 3 years. The company's board is composed of: 5 new directors. 2 experienced directors. 5 highly experienced directors. Chief Scientific Officer & Director Miriam Kidron is the most experienced director on the board, commencing their role in 2006. The following issues are considered to be risks according to the Simply Wall St Risk Model: Lack of board continuity. Lack of experienced directors. Announcement • Jun 03
Oramed Pharmaceuticals Inc., Annual General Meeting, Jun 30, 2022 Oramed Pharmaceuticals Inc., Annual General Meeting, Jun 30, 2022, at 13:00 Coordinated Universal Time. Location: Israeli office, located at 20 Mamilla Avenue, Jerusalem Jerusalem Israel Agenda: To re-elect five directors of the Company to hold office until our next annual meeting of stockholders and until their respective successors shall be elected and qualified or until their earlier resignation or removal; to consider and approve, by a non-binding advisory vote, the compensation of Named Executive Officers as described in the accompanying proxy statement; to consider and approve an amendment to the Company’s Amended and Restated 2019 Stock Incentive Plan (the “2019 Incentive Plan”); to ratify the appointment of Kesselman & Kesselman, certified public accountants in Israel, a member of PricewaterhouseCoopers International Limited, as the independent registered public accounting firm of the Company for the 2022 fiscal year; and to transact any other business as may properly come before the Annual Meeting or any adjournments thereof. Announcement • Jun 02
Oramed Pharmaceuticals Inc. Appoints Anne Peters to Its Scientific Advisory Board Oramed Pharmaceuticals Inc. announced the appointment of Anne Peters, MD, to its Scientific Advisory Board. Anne Peters, MD, is Professor of Medicine at the Keck School of Medicine of USC and Director of the USC Clinical Diabetes Programs. Dr. Peters earned her medical degree from the Pritzker School of Medicine at the University of Chicago and performed an internal medicine residency at Stanford University and an endocrinology fellowship at Cedars-Sinai Medical Center. She previously directed the clinical diabetes programs at Cedars-Sinai and UCLA. Her research has focused on testing new approaches for diagnosing and treating diabetes and developing systems of care to improve outcomes in diabetic populations. In addition to being an investigator for more than 40 research studies, Dr. Peters has published over 200 articles, has written four books, and has given more than 500 lectures locally, nationally, and internationally. She has been on multiple guideline writing committees for the treatment of both type 1 and type 2 diabetes. She was a recipient of the ADA Outstanding Physician Clinician Award, the Bernardo Houssay Award from the National Minority Quality Forum and received a 2021 Endocrine Society Laureate Award for Public Service. Currently, Dr. Peters is the chair of the Endocrine Society Committee on Diabetes Devices and is on the EASD/ADA Technology Safety Committee. Additionally, she is a member of the JDRF Panel on Management of Exercise in type 1 Diabetes and a member of the ABIM Endocrinology Subspecialty Board. Dr. Peters has consulted for many entities, including the FDA, Optum Rx and CVS/Caremark to help guide the development and use of treatments for diabetes. Reported Earnings • May 14
First quarter 2022 earnings released: US$0.27 loss per share (vs US$0.17 loss in 1Q 2021) First quarter 2022 results: US$0.27 loss per share (down from US$0.17 loss in 1Q 2021). Net loss: US$10.4m (loss widened 126% from 1Q 2021). Over the next year, revenue is forecast to grow 2.5%, compared to a 7.1% growth forecast for the industry in Germany. Over the last 3 years on average, earnings per share has fallen by 6% per year but the company’s share price has increased by 13% per year, which means it is well ahead of earnings. Announcement • May 04
Oramed Pharmaceuticals Inc. Completes Patient Enrollment in Pivotal Phase 3 Oral Insulin Study Ora-D-013-1 Oramed Pharmaceuticals Inc. announced it has completed patient enrollment for its Phase 3 ORA-D-013-1 study of its oral insulin capsule ORMD-0801 for the treatment of type 2 diabetes (T2D), surpassing its target of 675 patients with 710 patients enrolled. ORA-D-013-1 is the larger of Oramed's two Phase 3 studies being conducted under U.S. Food and Drug Administration (FDA) approved protocols to treat T2D patients who have inadequate glycemic control over a period of 6 to 12 months. Efficacy data for ORA-D-013-1 will become available after all patients have completed the first 6-month treatment period. The ORA-D-013-1 study initially aimed to enroll 675 patients and has now completed its enrollment oversubscribed with a total of 710 patients. The enrolled patients are currently on 2 or 3 oral glucose-lowering agents through 96 clinical sites throughout the U.S. The primary endpoint of the study is to compare the efficacy of ORMD-0801 to placebo in improving glycemic control as assessed by A1c, with a secondary endpoint of assessing the change from baseline in fasting plasma glucose at 26 weeks. Efficacy data will become available after all patients have completed the first 6-month treatment period. Reported Earnings • Apr 02
Full year 2021 earnings released: US$0.94 loss per share (vs US$0.90 loss in FY 2020) Full year 2021 results: US$0.94 loss per share (down from US$0.90 loss in FY 2020). Net loss: US$35.0m (loss widened 59% from FY 2020). Over the next year, revenue is forecast to grow 1.4%, compared to a 8.2% growth forecast for the pharmaceuticals industry in Germany. Over the last 3 years on average, earnings per share has increased by 2% per year but the company’s share price has increased by 35% per year, which means it is tracking significantly ahead of earnings growth. Recent Insider Transactions • Mar 29
Independent Chairman of the Board recently sold €85k worth of stock On the 21st of March, Kevin Rakin sold around 10k shares on-market at roughly €8.52 per share. This was the largest sale by an insider in the last 3 months. Kevin has been a seller over the last 12 months, reducing personal holdings by €462k. Reported Earnings • Jan 12
First quarter 2022 earnings: EPS in line with expectations, revenues disappoint First quarter 2022 results: US$0.21 loss per share (up from US$0.23 loss in 1Q 2021). Net loss: US$7.89m (loss widened 42% from 1Q 2021). Revenue missed analyst estimates by 3.7%. Over the next year, revenue is forecast to grow 2.2%, compared to a 7.1% growth forecast for the industry in Germany. Over the last 3 years on average, earnings per share has increased by 9% per year but the company’s share price has increased by 52% per year, which means it is tracking significantly ahead of earnings growth. Announcement • Dec 15
Oramed Subsidiary Oravax Announces First Participant Enrolled in Phase 1 Oral Covid-19 Vaccine Trial in South Africa Oramed Pharmaceuticals Inc. announced that its subsidiary, Oravax Medical Inc., has screened and enrolled the first participant in a Phase 1 clinical trial of its oral virus-like particle (VLP) COVID-19 vaccine in Johannesburg, South Africa. The open-label trial anticipates enrolling 24 participants who have not received either a COVID-19 vaccine or contracted the virus. Participants will be administered one dose of the oral vaccine at the beginning of the trial and a second dose three weeks later. The trial's endpoints will include safety and tolerability as well as efficacy by measuring the presence of an immunogenic response. Oravax's oral VLP vaccine targets three SARS CoV-2 virus surface proteins, including proteins less susceptible to mutation, thus making the vaccine potentially more effective against current and future variants of the COVID-19 virus. Oravax's VLP vaccine technology is highly scalable for manufacturing and is easily transferable for logistical wide scale distribution as there is no need for subfreezing storage. Reported Earnings • Nov 25
Full year 2021 earnings: EPS in line with expectations, revenues disappoint Full year 2021 results: US$0.78 loss per share (down from US$0.56 loss in FY 2020). Net loss: US$22.2m (loss widened 93% from FY 2020). Revenue missed analyst estimates by 9.2%. Over the next year, revenue is forecast to stay flat compared to a 6.7% growth forecast for the pharmaceuticals industry in Germany. Over the last 3 years on average, earnings per share has increased by 12% per year but the company’s share price has increased by 68% per year, which means it is tracking significantly ahead of earnings growth. Announcement • Nov 24
Oramed Pharmaceuticals Inc. Reaches 75% Enrollment in Phase 3 Oral Insulin Study Oramed Pharmaceuticals Inc. announced that it has enrolled and randomized over 75% of the 675 patients planned for its Phase 3 ORA-D-013-1 study of its oral insulin capsule ORMD-0801 for the treatment of type 2 diabetes (T2D). ORA-D-013-1 is the larger of Oramed's two Phase 3 studies being conducted under U.S. Food and Drug Administration (FDA) approved protocols to treat T2D patients who have inadequate glycemic control over a period of 6 to 12 months. Efficacy data for ORA-D-013-1 will become available after all patients have completed the first 6-month treatment period. The concurrent study, ORA-D-013-2, commenced enrollment in March for a planned 450 patients. ORA-D-013-1 is recruiting 675 patients who are currently on 2 or 3 oral glucose-lowering agents through 75 clinical sites throughout the U.S. The primary endpoint of the study is to compare the efficacy of ORMD-0801 to placebo in improving glycemic control as assessed by A1c, with a secondary endpoint of assessing the change from baseline in fasting plasma glucose at 26 weeks. Efficacy data will become available after all patients have completed the first 6-month treatment period. The ORA-D-013-1 study is a double blind, double dummy study randomizing patients 1:1:1 for 8 mg ORMD-0801 once-daily at night and placebo 45 minutes before breakfast; or 8 mg ORMD-0801 twice-daily at night and 45 minutes before breakfast; or placebo twice daily at night and 45 minutes before breakfast. Recent Insider Transactions • Sep 22
Independent Chairman of the Board recently sold €376k worth of stock On the 16th of September, Kevin Rakin sold around 21k shares on-market at roughly €17.84 per share. This was the largest sale by an insider in the last 3 months. This was Kevin's only on-market trade for the last 12 months. Executive Departure • Sep 03
Independent Director Xiaoming Gao has left the company On the 30th of August, Xiaoming Gao's tenure as Independent Director ended after 2.2 years in the role. We don't have any record of a personal shareholding under Xiaoming's name. A total of 2 executives have left over the last 12 months. The current median tenure of the management team is 3.42 years. Announcement • Aug 25
Oramed Pharmaceuticals Inc. Reaches 25% Enrollment in Its Second of Two Concurrent Phase 3 Oral Insulin Trials Oramed Pharmaceuticals Inc. announced that it has enrolled and randomized over 25% of the planned 450 patients for its Phase 3 ORA-D-013-2 trial of its oral insulin capsule ORMD-0801 for the treatment of type 2 diabetes (T2D). ORA-D-013-2 is the second of Oramed's two Phase 3 trials being conducted under U.S. Food and Drug Administration (FDA) approved protocols to treat T2D patients who have inadequate glycemic control over a period of 6 to 12 months. The concurrent trial, ORA-D-013-1, completed enrollment and randomization of nearly 65% of its 675 planned patients and is on track to complete randomization with topline results expected in 2022. Announcement • Jul 23
Oramed Pharmaceuticals Inc. Provides Update on Oravax: Oral Vaccine Maker Gets IRB Approval for Clinical Trial Oramed Pharmaceuticals Inc. announced several updates for its majority-owned company OravaxMedical Inc. Oravax capitalizes on Oramed's proprietary protein oral delivery (POD™) technology in the development of oral vaccines that are now only available via injection. Oravax is the exclusive owner of a virus-like particle (VLP) vaccine technology that targets three SARS CoV-2 virus surface proteins, including proteins less susceptible to mutation, thus making the vaccine potentially effective against current and future variants of the COVID-19 virus. The VLP vaccine is being tested in preclinical studies against COVID-19 variants including the Delta variant. Oravax's VLP vaccine technology is highly scalable with a low cost of goods and easily transferable. Oravax is gearing up to commence clinical trials for its oral COVID-19 vaccine, first in Israel, then in additional clinical sites internationally. The study protocol has been approved by the Institutional Review Board (IRB) at Ichilov Hospital in Tel Aviv, Israel and is now pending approval from the Israeli Ministry of Health. GMP manufacturing for the oral vaccine is under way. The oral VLP COVID-19 vaccine is being developed for use both as a standalone vaccine as well as a booster for people who have been previously vaccinated for COVID-19. Experts including at the World Health Organization expect booster shots will be needed for both general and at-risk populations. If successful, an oral vaccine would offer enormous logistical, financial, and environmental benefits for the billions of people slated to receive them, particularly in parts of the world where access to healthcare is limited. Reported Earnings • Jul 16
Third quarter 2021 earnings released: US$0.17 loss per share (vs US$0.098 loss in 3Q 2020) Third quarter 2021 results: Net loss: US$5.21m (loss widened 128% from 3Q 2020). Over the last 3 years on average, earnings per share has increased by 15% per year but the company’s share price has increased by 34% per year, which means it is tracking significantly ahead of earnings growth. Executive Departure • Jul 13
CFO, Treasurer & Secretary Avraham Gabay has left the company On the 5th of July, Avraham Gabay's tenure as CFO, Treasurer & Secretary ended after 2.1 years in the role. We don't have any record of a personal shareholding under Avraham's name. Avraham is the only executive to leave the company over the last 12 months. The current median tenure of the management team is 10.00 years. Announcement • Jun 09
Oramed Reaches 50% Enrollment in Phase 3 Oral Insulin Study Oramed Pharmaceuticals Inc. announced that it has enrolled and randomized over 50% of the 675 patients planned for its Phase 3 ORA-D-013-1 study of its oral insulin capsule ORMD-0801 for the treatment of type 2 diabetes. ORA-D-013-1 is the larger of Oramed's two Phase 3 studies being conducted under U.S. Food and Drug Administration approved protocols to treat T2D patients who have inadequate glycemic control over a period of 6 to 12 months. The concurrent study, ORA-D-013-2, commenced enrollment in March for a planned 450 patients. Efficacy data for ORA-D-013-1 will become available after all patients have completed the first 6-month treatment period. Reported Earnings • Apr 16
Second quarter 2021 earnings released: US$0.17 loss per share (vs US$0.21 loss in 2Q 2020) Second quarter 2021 results: Net loss: US$4.61m (loss widened 25% from 2Q 2020). Over the last 3 years on average, earnings per share has increased by 13% per year whereas the company’s share price has increased by 8% per year. Announcement • Mar 17
Oramed Pharmaceuticals Inc. Reaches 25% Randomization in World's First Phase 3 Oral Insulin Study Conducted Under FDA Approved Protocol Oramed Pharmaceuticals Inc. announced that it has enrolled and randomized 25% of the 675 patients planned for its Phase 3 ORA-D-013-1 study of its oral insulin capsule ORMD-0801 for the treatment of type 2 diabetes (T2D). ORA-D-013-1 is one of two concurrent Phase 3 studies conducted under U.S. Food and Drug Administration (FDA) approved protocols to treat T2D patients who have inadequate glycemic control over a period of 6 to 12 months. The double-blinded, placebo-controlled, multi-center randomized study will evaluate the efficacy and safety of ORMD-0801. Efficacy data will become available after all patients have completed the first 6-month treatment period. ORA-D-013-1 is recruiting 675 patients who are currently on 2 or 3 oral glucose-lowering agents through 75 clinical sites throughout the U.S. The primary endpoint of the study is to compare the efficacy of ORMD-0801 to placebo in improving glycemic control as assessed by A1c, with a secondary endpoint of assessing the change from baseline in fasting plasma glucose at 26 weeks. Efficacy data will become available after all patients have completed the first 6-month treatment period. The ORA-D-013-1 study is a double blind, double dummy study randomizing patients 1:1:1 for: 8 mg ORMD-0801 once-daily at night and placebo 45 minutes before breakfast; or 8 mg ORMD-0801 twice-daily at night and 45 minutes before breakfast; or placebo twice daily at night and 45 minutes before breakfast. Is New 90 Day High Low • Feb 17
New 90-day high: €9.23 The company is up 333% from its price of €2.13 on 19 November 2020. The German market is up 11% over the last 90 days, indicating the company outperformed over that time. It also outperformed the Pharmaceuticals industry, which is up 13% over the same period. Is New 90 Day High Low • Jan 26
New 90-day high: €5.31 The company is up 155% from its price of €2.08 on 27 October 2020. The German market is up 16% over the last 90 days, indicating the company outperformed over that time. It also outperformed the Pharmaceuticals industry, which is up 15% over the same period. Announcement • Jan 22
Oramed Pharmaceuticals Inc. Doses Patients Across Multiple Sites in Phase 3 Oral Insulin Study Oramed Pharmaceuticals Inc. announced that randomization of patients in its first Phase 3 study of its oral insulin capsule ORMD-0801 for the treatment of type 2 diabetes (T2D) is under way. The study is being conducted in accordance with U.S. Food and Drug Administration (FDA) approved protocols. ORA-D-013-1 is recruiting 675 patients who are currently on two or three oral glucose-lowering agents through 75 clinical sites throughout the U.S. The primary endpoint of the study is to compare the efficacy of ORMD-0801 to placebo in improving glycemic control as assessed by A1c, with a secondary endpoint of assessing the change from baseline in fasting plasma glucose at 26 weeks. Efficacy data will become available after all patients have completed the first 6-month treatment period. The ORA-D-013-1 trial is a double blind, double dummy study randomizing patients 1:1:1 for: 8 mg ORMD-0801 once-daily at night and placebo 45 minutes before breakfast; or 8 mg ORMD-0801 twice-daily at night and 45 minutes before breakfast; or placebo twice-daily at night and 45 minutes before breakfast. Analyst Estimate Surprise Post Earnings • Jan 18
Revenue beats expectations Revenue exceeded analyst estimates by 1.3%. Over the next year, revenue is forecast to grow 29%, compared to a 2.5% growth forecast for the Pharmaceuticals industry in Germany. Analyst Estimate Surprise Post Earnings • Jan 16
Revenue beats expectations Revenue exceeded analyst estimates by 1.3%. Over the next year, revenue is forecast to grow 29%, compared to a 2.5% growth forecast for the Pharmaceuticals industry in Germany. Reported Earnings • Jan 15
First quarter 2021 earnings released: US$0.23 loss per share First quarter 2021 results: Net loss: US$5.57m (loss widened 119% from 1Q 2020). Over the last 3 years on average, earnings per share has increased by 10% per year but the company’s share price has fallen by 19% per year, which means it is significantly lagging earnings. Announcement • Dec 25
Oramed Pharmaceuticals Inc. Reports Positive First in Human Data from Oral Leptin Study Oramed Pharmaceuticals Inc. announced results from a proof-of-concept study approved by Israel's Ministry of Health for its oral leptin drug candidate. The single dose study evaluated oral leptin's safety and pharmacodynamics (glucagon and glucose reduction) in type 1 diabetic (T1DM) patients. Ten patients were enrolled, with 7 randomized to receive one capsule of leptin and 3 randomized to receive a placebo. Patients who received leptin on average had a decrease in glucose as compared to the placebo group during the first 30-180 minutes following dosing. At different time periods, the leptin treated patients on average had glucagon values that were either lower than, or similar to, those in the placebo group. Leptin, also known as the obesity hormone, is a protein that regulates hunger. According to Grand View Research, the overall obesity market is expected to reach $15.6 billion in 2024. Leptin, sometimes called the obesity, fat or satiety hormone, is a protein that is produced in fat cells located in adipose tissues and sends signals to the hypothalamus in the brain. Leptin helps to regulate and alter long-term food intake and energy expenditure. Leptin helps to inhibit hunger and regulate energy balance. Although leptin reduces appetite, obese individuals generally exhibit a higher concentration of leptin in their blood than average weight individuals. These people show resistance to leptin, similar to resistance of insulin in type 2 diabetes. Leptin has additionally been shown to suppress glucagon secretion and improve glucose levels in type 1 diabetes. Announcement • Dec 03
Oramed Pharmaceuticals Inc. Initiates Phase 2 NASH Trial of Oral Insulin Oramed Pharmaceuticals Inc. announced it has screened the first patients in a global trial of its oral insulin capsule ORMD-0801 for the treatment of Nonalcoholic steatohepatitis (NASH). The patients were screened at a U.S. site participating in Oramed's trial, being conducted at U.S., EU and Israeli clinical sites. The trial will be comprised of eight clinical sites: three in the EU, three in the U.S. and two in Israel. The trial will measure efficacy endpoints via MRI-PDFF for 12-weeks dosing. Is New 90 Day High Low • Nov 28
New 90-day high: €3.34 The company is up 15% from its price of €2.90 on 28 August 2020. The German market is up 3.0% over the last 90 days, indicating the company outperformed over that time. It also outperformed the Pharmaceuticals industry, which is up 4.0% over the same period. According to the Simply Wall St valuation model, the estimated intrinsic value of the company is €34.11 per share. Analyst Estimate Surprise Post Earnings • Nov 25
Revenue misses expectations Revenue missed analyst estimates by 31%. Over the next year, revenue is forecast to grow 32%, compared to a 2.5% growth forecast for the Pharmaceuticals industry in Germany. Announcement • Nov 25
Oramed Pharmaceuticals Inc Initiates Phase 3 Trial of Oral Insulin Oramed Pharmaceuticals Inc. announced it has screened the first patients in its global Phase 3 trials of its oral insulin capsule ORMD-0801 for the treatment of type 2 diabetes (T2D). The patients were screened at U.S. sites participating in Oramed's ORA-D-013-1 trial, one of two Phase 3 trials being conducted in accordance with U.S. Food and Drug Administration approved protocols. Both Phase 3 trials, ORA-D-013-1 and ORA-D-013-2, will treat T2D patients who have inadequate glycemic control over a period of 6 to 12 months. The double-blinded, placebo-controlled, multi-center randomized trials will recruit a total of 1,125 patients to evaluate the efficacy and safety of ORMD-0801. Â Efficacy data will become available after all patients have completed the first 6-month treatment period. Reported Earnings • Nov 25
Full year 2020 earnings released: US$0.56 loss per share Full year 2020 results: Net loss: US$11.5m (loss narrowed 20% from FY 2019). Over the last 3 years on average, earnings per share has increased by 8% per year but the company’s share price has fallen by 34% per year, which means it is significantly lagging earnings. Is New 90 Day High Low • Oct 16
New 90-day low: €2.13 The company is down 39% from its price of €3.47 on 17 July 2020. The German market is flat over the last 90 days, indicating the company underperformed over that time. It also underperformed the Pharmaceuticals industry, which is down 12% over the same period. According to the Simply Wall St valuation model, the estimated intrinsic value of the company is €38.35 per share. Is New 90 Day High Low • Sep 18
New 90-day low: €2.32 The company is down 35% from its price of €3.58 on 19 June 2020. The German market is up 6.0% over the last 90 days, indicating the company underperformed over that time. It also underperformed the Pharmaceuticals industry, which is down 3.0% over the same period. According to the Simply Wall St valuation model, the estimated intrinsic value of the company is €39.95 per share.