WebMar 3, 2024 · WILMINGTON, Del. Incyte (Nasdaq:INCY) today announced that it will discontinue the Phase 3 LIMBER-304 trial following results of a pre-planned interim analysis conducted by an independent data monitoring committee (IDMC) indicating that the study is unlikely to meet the primary endpoint in the intent-to-treat patient population. WebMar 3, 2024 · Incyte (Nasdaq:INCY) today announced that it will discontinue the Phase 3 LIMBER-304 trial following results of a pre-planned interim analysis conducted by an independent data monitoring committee (IDMC) indicating that the study is unlikely to meet the primary endpoint in the intent-to-treat patient population.
Incyte to Discontinue Phase 3 LIMBER-304 Trial of Parsaclisib …
WebSep 16, 2024 · Incyte Corporation: ClinicalTrials.gov Identifier: NCT04551053 Obsolete Identifiers: NCT04816565: Other Study ID Numbers: INCB 50465-304/LIMBER-304 : First … WebDec 10, 2024 · Incyte announced new data from two of its LIMBER trials evaluating monotherapy and combination strategies using ruxolitinib with parsaclisib, its … chinese and indian relations
Second Setback For Incyte
WebIncyte is an American multinational pharmaceutical company with headquarters in Wilmington, Delaware, and Morges, Switzerland. The company was created in 2002 … WebMar 3, 2024 · The LIMBER clinical trial program is designed to evaluate multiple monotherapy and combination strategies to improve and expand treatments for patients with MPNs and GVHD. These include ruxolitinib-based combinations with BET and ALK2, new therapeutic options including axatilimab and novel targets such as mutant CALR. … WebMar 6, 2024 · Incyte has stressed that the recommendation to stop the study was not due to safety. LIMBER-304 is a randomized, double-blind study evaluating the efficacy and safety of parsaclisib plus Jakafi (ruxolitinib), versus placebo plus ruxolitinib, in adult patients living with myelofibrosis who have an inadequate response to ruxolitinib monotherapy. grand center point asoke