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VTRS Down on Late-Stage Study Failure of Eye Disease Drug
ZACKS· 2025-07-21 14:51
Core Insights - Viatris, Inc. (VTRS) announced that its late-stage study on the ophthalmic ointment MR-139 failed to meet primary endpoints in patients with blepharitis, leading to a 4.21% drop in share price [1][6] - Year-to-date, VTRS shares have decreased by 26.8%, contrasting with a 9% decline in the industry [1] Study Details - The MR-139 study was a randomized, placebo-controlled, double-masked phase III trial involving approximately 477 patients, who self-administered the treatment twice daily for 12 weeks [3] - The primary endpoint of complete resolution of eyelid debris after six weeks was not achieved [3][6] Future Plans - VTRS is evaluating next steps for the MR-139 phase III program, which may involve revising the planned additional study [4][6] - The company is focusing on its ophthalmology portfolio, which includes therapies like Tyrvaya and Ryzumvi, and aims to address unmet needs in anterior segment conditions [4] Portfolio Strengthening - VTRS has established an ophthalmology franchise through acquisitions of Oyster Point Pharma and FamyLife Sciences [6] - The company is restructuring its business following the sale of its biosimilar portfolio and divesting its over-the-counter and Active Pharmaceutical Ingredients businesses in India, as well as its women's healthcare segment, to streamline core operations [7]
Viatris Hits Snag In Eye Drug Study—Phase 3 Plans Under Review
Benzinga· 2025-07-18 18:17
Core Insights - Viatris Inc. announced topline data from a Phase 3 study of pimecrolimus 0.3% ophthalmic ointment for blepharitis, a common eye condition characterized by eyelid inflammation [1] - The trial did not meet its primary endpoint of complete resolution of debris after six weeks of treatment [2] - The company is evaluating next steps for the Phase 3 program, which may include revising the planned additional Phase 3 study [3] Product Development - Viatris is focused on delivering novel therapies such as Tyrvaya and Ryzumvi while progressing a differentiated pipeline [3] - In June, Viatris and Opus Genetics announced topline results from the VEGA-3 trial evaluating MR-141 for presbyopia treatment [4] - MR-141 showed that more patients achieved significant visual acuity gains compared to placebo at various time points [5][6] Market Performance - Viatris shares have an average 1-year price target of $10, indicating an expected upside of 11.86% [7] - At the time of publication, Viatris shares were down 3.94% at $8.90 [7]
Viatris Provides Update on Phase 3 Study of MR-139 for Blepharitis
Prnewswire· 2025-07-18 10:59
Core Insights - Viatris Inc. announced that its Phase 3 study for pimecrolimus 0.3% (MR-139) ophthalmic ointment did not meet its primary endpoint of complete resolution of debris in patients with blepharitis after six weeks of treatment [1][2][5] - The company is evaluating next steps for the Phase 3 program, which may include revising the planned additional Phase 3 study [2][5] - Viatris is focused on delivering novel therapies and has reported positive results from other ongoing clinical trials, including MR-142 and MR-141 [2][5] Study Details - The MR-139 3001 Phase 3 trial involved 477 patients who were randomized to receive either MR-139 or a placebo, with treatment administered twice daily over a 12-week period [3] Company Overview - Viatris is a global healthcare company that combines generics and brand medications to address healthcare needs worldwide, supplying high-quality medicines to approximately 1 billion patients annually [4] - The company is headquartered in the U.S. and has global centers in Pittsburgh, Shanghai, and Hyderabad, India [4]
Founder Mina Sooch Issues Open Letter to Opus Genetics Stockholders Following Withdrawal of the Restore Value Slate Amid Dilutive Financing and Governance Concerns
Newsfilter· 2025-04-11 19:47
Board Timed Highly Dilutive Financing to Close on the Record Date for the Annual Meeting, Tilting the Vote and Forcing the Withdrawal of the Restore Value Slate Second Major Transaction in Six Months Undertaken Without Stockholder Input with Significant Equity Dilution Company's Shifting Narrative on APX3330 in Disclosures Raises Questions of Omissions, Consistency, and Integrity of Strategic Communications FDA-Approved RYZUMVI™ Received Minimal Valuation in Both the Merger and Financing Transactions Desp ...