Can Merck’s remigromig compete with anti-VEGF treatments after BRUNELLO results?
Merck's remigromig met BRUNELLO's vision endpoint, but higher retinal complication rates complicate its potential in diabetic macular edema.
Merck's remigromig met BRUNELLO's vision endpoint, but higher retinal complication rates complicate its potential in diabetic macular edema.
Akeso starts Phase III cadonilimab testing in colon cancer, with 386 patients planned and recurrence outcomes central to its clinical strategy.
FDA approves Hovilpri for refractory HSV in immunocompromised adults after Phase 3 pritelivir beat investigator-choice therapy on lesion healing.
UCB's $2 billion Georgia biologics campus advances as drug demand rises, but manufacturing readiness and production timelines remain decisive.
Teva’s Weltruza wins FDA approval as a monthly subcutaneous olanzapine without loading doses, oral supplementation or post-injection monitoring.
Sling reports 82% sustained response among linsitinib responders after 48 weeks off therapy. See why Phase 3 ORBIT is the next critical test.
Biohaven gets $80 million upfront from Ono for Asian BHV-1300 rights as a 300-patient Phase 3 Graves’ disease trial tests the IgG degrader.
FDA approval moves Tecentriq into adjuvant stage III dMMR colon cancer after ATOMIC showed a 50% reduction in recurrence or death risk.
Illumina says SpliceAI2 found 17% more disease-relevant splice variants, but clinical use will require more than stronger AI prediction.
Vaxcyte’s VAX-31 met pivotal Phase 3 immune-response endpoints as the company prices $1 billion to fund trials and manufacturing scale-up.