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pd-l1 inhibitor incb086550

Generic: PD-L1 Inhibitor INCB086550

pd-l1 inhibitor incb086550: 4 clinical trials tracked.

pd-l1 inhibitor incb086550 evidence translation

What we can confirm

4 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about pd-l1 inhibitor incb086550, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence6 indications · 1 study sponsors
Clinical Trial Registry Records (4)

An Open-Label Study Assessing the Mass Balance, Pharmacokinetics, and Metabolite Profiles of a Single Oral Dose of [14C]-INCB086550

NCT05101369Registry updated 2025-08-21·Phase 1·INCY
Completed

Primary endpoint: Total recovery of radioactivity from urine and feces.

Interventionalopen7 enrolledStarted 2022-01Completion 2022-031 site · United KingdomIncyte Corporation

A Phase 2 Study of INCB086550 (Oral PD-L1 Inhibitor) in Participants Who Are Immune Checkpoint Inhibitor-Naïve With Selected Solid Tumors

NCT04629339Registry updated 2025-03-13·Phase 2·INCY
Terminated

Primary endpoint: Objective Response Rate (ORR)

Interventionalopen16 targetStarted 2021-09Completion 2024-0320 sites · Bulgaria, Hungary, South Korea, Taiwan…Incyte Corporation

A Phase 1 Study Exploring the Safety, Tolerability, and Pharmacokinetics of INCB086550 in Japanese Participants With Advanced Solid Tumors

NCT04674748Registry updated 2025-09-24·Phase 1
Terminated

Primary endpoint: Number of Participants with Treatment Emergent Adverse Events (TEAE)

Interventionalopen3 targetStarted 2021-02Completion 2022-052 sites · JapanIncyte Biosciences Japan GK

A Phase 1 Study Exploring the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of INCB086550 in Participants With Advanced Solid Tumors

NCT03762447Registry updated 2025-08-11·Phase 1·INCY
Completed

Primary endpoint: Number of treatment-emergent adverse events

Interventionalopen138 enrolledStarted 2018-12Completion 2023-1125 sites · Belgium, France, Italy, United Kingdom…Incyte Corporation