Incyte announces positive Phase 2 results for zilurgisertib in FOP
The PROGRESS study showed reduced heterotopic ossification and FDA accepted NDA under Priority Review.
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Global biopharmaceutical company
incyte.comLast updated
In short: Incyte reported strong 2026 financial growth, advanced several key late-stage clinical programs, and expanded its pipeline through major acquisitions.
The PROGRESS study showed reduced heterotopic ossification and FDA accepted NDA under Priority Review.
The Tafa-Len-R-CHOP regimen reduced risk of disease progression or death by 25% compared to R-CHOP. Data presented at EHA 2026 Congress.
The drug achieved rapid, robust clinical and molecular responses and was well tolerated in MF and ET patients.
The acquisition adds VGA039, a Phase 3 monoclonal antibody for von Willebrand disease, with $1.25B upfront and up to $750M in milestones.
Incyte shares stay in focus on Nasdaq as investors weigh fresh clinical trial results, a recent S&P 500 swing and updated long-term revenue projections while...
On June 14, 2026, Incyte Corp (INCY) announced new clinical findings from two Phase 1 trials focused on INCA033989, a monoclonal antibody targeting mutant calre...
- Cohort 1 results presented at ENDO 2026 demonstrate meaningful reductions in total heterotopic ossification (HO) lesion volume, new HO lesions and flare activity in...
New Positive Data Showed INCA033989 Achieved Rapid, Robust & Sustained Clinical & Molecular Responses and Was Well Tolerated in Patients with MF & ET...
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