BENITIONSClinical Trial Intelligence

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

Фаза 1/2 Прекращено NCT05949632

ЗаболеваниеAdvanced Solid Tumors
ФазаФаза 1/2
СпонсорIncyte Corporation
СтатусПрекращено
Участники5 участн.
ВмешательствоINCB099280, axitinib
Дата начала16.04.2024
Дата завершения6.06.2025
Публикация результатов4.06.2026

Кратко

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

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