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Scott+Scott Attorneys at Law LLP & Hedin Hall LLP Announce Notice of Class Action and Proposed Settlement to All Who Purchased or Acquired Shares of Viatris Inc. Pursuant to a November 2020 Merger of Mylan N.V. and Upjohn, Inc. to Form Viatris - Vimarsana News

Scott+Scott Attorneys at Law LLP & Hedin Hall LLP Announce Notice of Class Action and Proposed Settlement to All Who Purchased or Acquired Shares of Viatris Inc. Pursuant to a November 2020 Merger of Mylan N.V. and Upjohn, Inc. to Form Viatris

NEW YORK, March 11, 2024 /PRNewswire/ -- IN THE COURT OF COMMON PLEAS OF ALLEGHENY COUNTY, PENNSYLVANIA RAJESH PATEL, Individually and on Behalf of All Others Similarly...

Viatris Reports Strong Third Quarter 2022 Results - Vimarsana News

Viatris Reports Strong Third Quarter 2022 Results

Reaffirms 2022 Guidance Ranges [1] Across Total Revenues, Adjusted EBITDA and Free Cash Flow; Driven by Solid Operating Momentum Despite Foreign Exchange...

Viatris : Strategic Update Presentation - Vimarsana News

Viatris : Strategic Update Presentation

Strategic Update: Our Path to Return to Growth November 7, 2022 Forward Looking Statements ... | November 7, 2022

Viatris Reports Strong First-Quarter 2022 Results - Vimarsana News

Viatris Reports Strong First-Quarter 2022 Results

/PRNewswire/ -- First-Quarter 2022 Results Reflect Strong Operational Start to the Year Total Revenues Were $4.19 billion U.S. GAAP Net Earnings Were $399.2...

Pfizer reports fourth-quarter and full-year 2020 results and releases 5-YEAR pipeline metrics - Vimarsana News

Pfizer reports fourth-quarter and full-year 2020 results and releases 5-YEAR pipeline metrics

5% Below are specific updates on pipeline assets since our previous earnings announcement on October 27, 2020: Abrocitinib (PF-04965842) — In November 2020, Pfizer announced positive top-line results from the fifth Phase 3 trial of abrocitinib, JADE REGIMEN, a 52-week study which investigated abrocitinib in patients 12 and older with moderate to severe atopic dermatitis (AD) following response to initial open label induction treatment with abrocitinib 200 mg. Patients were randomized into one of three arms: 200 mg, 100 mg or placebo. Both doses of abrocitinib met the primary endpoint, resu...