BENITIONSClinical Trial Intelligence

A Study of INCB099280 in Combination With Axitinib in Adults With Advanced Solid Tumors

Phase 1/2 Terminated NCT05949632

ConditionAdvanced Solid Tumors
PhasePhase 1/2
SponsorIncyte Corporation
StatusTerminated
Enrollment5 participants
InterventionsINCB099280, axitinib
Start dateApr 16, 2024
Completion dateJun 6, 2025
Results postedJun 4, 2026

Summary

This study is being conducted to evaluate the safety and tolerability of INCB099280 in combination with axitinib and to assess the antitumor activity of INCB099280 in combination with axitinib. This study will only be open in the UK and EU.

Part 1: Number of Participants With Dose-limiting Toxicities (DLTs)

up to 3 weeks · Participants

INCB099280 400 mg BID Plus Axitinib 5 mg BID1 Participants

Part 1: Number of Participants With Any Treatment-emergent Adverse Event (TEAE)

up to approximately 1 year · Participants

INCB099280 400 mg BID Plus Axitinib 5 mg BID5 Participants

Part 1: Number of Participants With TEAEs Leading to a Dosing Modification (Treatment Interruption, Dose Reduction, and Permanent Discontinuation of Either Study Drug)

up to approximately 1 year · Participants

INCB099280 400 mg BID Plus Axitinib 5 mg BID5 Participants
INCB099280 400 mg BID Plus Axitinib 5 mg BID0 Participants
INCB099280 400 mg BID Plus Axitinib 5 mg BID4 Participants
INCB099280 400 mg BID Plus Axitinib 5 mg BID3 Participants
INCB099280 400 mg BID Plus Axitinib 5 mg BID1 Participants

Open in BENITIONS View on ClinicalTrials.gov

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