Core Insights - Viatris Inc. announced positive top-line results from the VEGA-3 Phase 3 trial for MR-141, demonstrating significant improvement in near visual acuity for patients with presbyopia without compromising distance vision [1][2] - The trial involved 545 patients and showed that MR-141 significantly outperformed placebo in achieving primary and secondary endpoints [5][6] - The company plans to submit an application to the U.S. FDA in the second half of 2025 [1][8] Company Overview - Viatris is a global healthcare company that combines generics and brand medications to address healthcare needs, supplying high-quality medicines to approximately 1 billion patients annually [7] - The company is headquartered in the U.S. with global centers in Pittsburgh, Shanghai, and Hyderabad [7] Industry Context - Presbyopia affects nearly 128 million people in the U.S., approximately 90% of adults over 45, and is projected to impact 2.1 billion people globally by 2030 [6] - The condition leads to significant economic losses, estimated between $11 billion and $25 billion due to uncorrected cases, highlighting the need for effective near-vision correction solutions [6]
Viatris Announces Positive Top-Line Results from Second Pivotal Phase 3 VEGA-3 Trial of MR-141 in Presbyopia