Incb-099280
WebLARVOL VERI predictive biomarker analytics, INCB99280. Full access to predictive biomarker details and heatmap analytics are available with a VERI Account. WebOrg Study ID: INCB 99280-112; Secondary ID: N/A; NTC ID: NCT04242199; Sponsor: Incyte Corporation; BRIEF SUMMARY The purpose of this study is to evaluate the safety and …
Incb-099280
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WebNov 5, 2024 · INCB 00928-104 is designed to evaluate the safety and tolerability of INCB000928 as monotherapy or in combination with ruxolitinib in patients with anemia due to MF. Methods: INCB 00928-104 (NCT04455841) is a phase 1/2, open-label, multicenter, dose-escalation and -expansion study assessing INCB000928 alone (treatment group A … WebBackground INCB099280 is an orally administered, small-molecule inhibitor of programmed cell death ligand 1 (PD-L1). This is an ongoing, phase 1, open-label, multicenter study. …
WebJul 30, 2024 · Incb099280 has been investigated in 1 clinical trial, of which 1 is open and 0 are closed. Of the trial investigating incb099280, 1 is phase 1 (1 open). Deficient DNA … WebJan 23, 2024 · Drug: INCB099280 Study Type Interventional Enrollment (Anticipated) 203 Phase Phase 1 Contacts and Locations This section provides the contact details for those …
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WebThe purpose of this study is to evaluate the safety and tolerability, pharmacokinetics, and pharmacodynamics of INCB099318 in select solid tumors. Overall Status Recruiting Start Date March 26, 2024 Phase Phase 1 Study Type Interventional PRIMARY OUTCOMES Primary Outcome 1 - Measure: Number of treatment-emergent adverse events
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