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Viatris Inc Ord Shs Stock Price, News & Analysis

VTRS Nasdaq

Welcome to our dedicated page for Viatris Ord Shs news (Ticker: VTRS), a resource for investors and traders seeking the latest updates and insights on Viatris Ord Shs stock.

Viatris Inc. (Nasdaq: VTRS) is a global healthcare company that regularly issues news on its operations, strategy and pipeline across generics, established brands and innovative medicines. This news page aggregates company announcements, press releases and third-party coverage related to VTRS, giving readers a single place to review the latest corporate developments.

Viatris frequently reports on regulatory milestones in its global pipeline. Recent updates include FDA approval of octreotide acetate for injectable suspension as a generic version of Sandostatin LAR Depot, FDA acceptance of a New Drug Application for a low dose estrogen weekly contraceptive patch, FDA clearance of an IND for the MR‑146 gene therapy candidate in neurotrophic keratopathy, and acceptance of a Japanese New Drug Application for pitolisant in obstructive sleep apnea syndrome. The company also announces progress in Japan and the Asia-Pacific region, such as the acquisition of Aculys Pharma and rights to pitolisant and Spydia nasal spray.

Investors can also find financial and corporate news, including quarterly results, updates to financial guidance, capital return actions like dividends and share repurchases, and information on enterprise-wide strategic reviews. Viatris’ participation in major healthcare and investor conferences, such as the J.P. Morgan Healthcare Conference and other sector events, is typically announced through press releases that are reflected in the news flow.

Additional news items may cover business development and collaborations, such as research agreements to develop engineered bacteriophage products for ophthalmic infections, as well as governance updates, board appointments and changes to corporate bylaws. For anyone tracking VTRS, this page offers a concise view of how Viatris communicates its strategy to strengthen its core portfolio, expand innovative brands and optimize its global structure.

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Viatris (NASDAQ: VTRS) has appointed David Simmons to its Board of Directors, bringing significant pharmaceutical industry and executive leadership experience. Simmons' notable career includes serving as CEO of Caliber Holdings Corporation, Operating Partner at Hellman & Friedman, and Chairman and CEO of PPD, Inc., where he led a 30,000-employee workforce and tripled the company's enterprise value, culminating in its $17.4 billion sale to Thermo Fisher Scientific in 2021.

Previously at Pfizer, Simmons served as President and General Manager of both the Established Products Unit and Emerging Markets division, managing 20,000 employees and 30% of Pfizer's global sales. His board experience includes positions at Cordis, Curia Global, Launch Therapeutics, Medline Industries, and Owens & Minor.

["Appointment of highly experienced pharmaceutical industry executive with proven leadership track record", "Direct experience with Viatris' established products portfolio from Pfizer tenure", "Extensive global commercial and R&D expertise", "Strong capital markets background including IPO and M&A experience"]
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Viatris (Nasdaq: VTRS) announced the presentation of five scientific abstracts at the upcoming PAINWeek 2025 conference, showcasing data from its Phase 3 program for a novel fast-acting meloxicam formulation (MR-107A-02) in treating moderate-to-severe acute surgical pain.

The presentations, scheduled for September 2-5, 2025, in Las Vegas, will feature results from two pivotal studies in herniorrhaphy and bunionectomy surgery models. The data includes pharmacokinetics, efficacy, safety, and opioid use reduction findings. Four abstracts will have live presentations on September 4, while one will be a poster-only presentation.

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Viatris (Nasdaq: VTRS) reported that its Phase 3 study of pimecrolimus 0.3% (MR-139) ophthalmic ointment for blepharitis failed to meet its primary endpoint of complete debris resolution after six weeks of twice-daily treatment.

The company is now evaluating next steps for the Phase 3 program, which may include revising the planned additional Phase 3 study. Despite this setback, Viatris highlighted recent successes with other pipeline products, including positive Phase 3 results from the LYNX-2 trial of MR-142 for keratorefractive conditions and the VEGA-3 Trial of MR-141 for presbyopia.

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Viatris (NASDAQ:VTRS) announced positive top-line results from its VEGA-3 Phase 3 trial for MR-141, a treatment for presbyopia. The randomized, placebo-controlled study involving 545 patients met its primary and all secondary endpoints, demonstrating significant improvement in near vision without compromising distance vision.

The trial showed statistically significant results (p<0.0001) in achieving ≥3-line gain in binocular distance-corrected near visual acuity. Patients reported significant functional benefits and satisfaction with near vision improvements, particularly in dim lighting conditions. The safety profile remained consistent with previous trials, with no treatment-related serious adverse events.

Viatris plans to submit an FDA application in H2 2025 for MR-141, targeting a condition that affects approximately 90% of U.S. adults over 45.

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Viatris (NASDAQ: VTRS) has announced it will release its second quarter 2025 financial results on Thursday, August 7, 2025. The company will hold a webcast at 8:30 a.m. ET on the same day where executives will discuss the quarterly performance. Investors and the public can access the live webcast through investor.viatris.com or by calling 844.308.3344 (US) or 412.317.1896 (international). A replay of the webcast will be made available on the company's website for later viewing.
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Viatris (NASDAQ: VTRS) announced positive Phase 3 LYNX-2 trial results for MR-142, a potential first-in-class treatment for night driving impairment in keratorefractive patients. The trial, involving 199 patients under FDA Special Protocol Assessment, met its primary endpoint with significantly more patients achieving ≥15-letter gain in mesopic low contrast visual acuity compared to placebo. MR-142 demonstrated patient-reported benefits in reducing difficulties with oncoming headlights and glare while driving. The drug showed no tachyphylaxis over 6 weeks and maintained a consistent safety profile. The FDA granted Fast Track designation for MR-142, potentially accelerating its development for treating chronic night driving impairment. A second pivotal study, LYNX-3, is expected to begin soon with results anticipated in H1 2026.
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Viatris (VTRS) reported Q1 2025 financial results with total revenues of $3.3 billion, down 11% year-over-year, but in line with expectations. The company posted a net loss of $3.0 billion, primarily due to a $2.9 billion goodwill impairment charge. Key metrics include adjusted EBITDA of $923 million and adjusted EPS of $0.50. Viatris returned over $450 million to shareholders year-to-date through share repurchases and dividends. The company made significant pipeline progress with three positive Phase 3 data readouts, including EFFEXOR for Japan, a novel meloxicam formulation, and XULANE LO contraceptive patch. Viatris reaffirmed its 2025 guidance with total revenues expected between $13.5-14.0 billion and adjusted EPS of $2.16-2.30.
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Viatris (NASDAQ: VTRS) announced positive Phase 3 study results for its investigational XULANE LO™ low dose contraceptive patch. The study, involving 1,272 women across 81 sites in the U.S., Puerto Rico, and Canada, demonstrated favorable efficacy with a Pearl Index of 4.14 and a 3.7% cumulative pregnancy probability over 13 cycles.

The patch showed strong performance metrics, including excellent adhesion with only 1.3% of patches completely detaching during the seven-day wearing period and less than 1% of subjects reporting severe local application site reactions. Most treatment emergent adverse events were mild-to-moderate, with favorable cycle control and low unscheduled bleeding events. Viatris plans to submit a New Drug Application to the FDA in the second half of 2025.

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Viatris (NASDAQ: VTRS) announced positive Phase 3 results for its novel fast-acting meloxicam (MR-107A-02) for treating moderate-to-severe acute pain. Two pivotal studies following herniorrhaphy and bunionectomy surgeries demonstrated statistically significant and clinically meaningful improvements in pain control compared to placebo and opioid treatment. Key findings include: - Significant pain improvement vs placebo in both surgeries (p<0.001) - Higher rates of opioid-free patients: 72.6% vs 58.6% in herniorrhaphy, 56.9% vs 33.1% in bunionectomy - Superior pain control compared to tramadol - Generally well-tolerated safety profile Viatris plans to submit a New Drug Application to the FDA by end of 2025, positioning MR-107A-02 as a potential first-line, non-opioid treatment option for acute pain management.
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Viatris (NASDAQ: VTRS) has announced a quarterly dividend payment of $0.12 per share for its common stock shareholders. The dividend was declared by the company's Board of Directors on May 5, 2025. Shareholders who own VTRS stock as of the close of business on May 23, 2025 (record date) will receive the dividend payment on June 16, 2025.

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FAQ

What is the current stock price of Viatris Ord Shs (VTRS)?

The current stock price of Viatris Ord Shs (VTRS) is $15.74 as of February 17, 2026.

What is the market cap of Viatris Ord Shs (VTRS)?

The market cap of Viatris Ord Shs (VTRS) is approximately 18.2B.

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VTRS Stock Data

18.16B
1.50B
Drug Manufacturers - Specialty & Generic
Pharmaceutical Preparations
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