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lysine-specific demethylase 1 inhibitor incb059872

Generic: Lysine-specific Demethylase 1 Inhibitor INCB059872

lysine-specific demethylase 1 inhibitor incb059872: 3 clinical trials tracked.

lysine-specific demethylase 1 inhibitor incb059872 evidence translation

What we can confirm

3 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 lysine-specific demethylase 1 inhibitor incb059872, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 1 study sponsors

Related indications

Clinical Trial Registry Records (3)

An Open-Label Phase 1b Study of the Safety, Tolerability, and Preliminary Antitumor Activity of INCB059872 in Participants With Relapsed or Refractory Ewing Sarcoma

NCT03514407Registry updated 2025-10-21·Phase 1·INCY
Terminated

Primary endpoint: Number of adverse events

Interventionalopen25 targetStarted 2018-06Completion 2020-0611 sites · Italy, Spain, United Kingdom, United StatesIncyte Corporation

A Phase 1/2 Study Exploring the Safety, Tolerability, Effect on the Tumor Microenvironment, and Efficacy of Azacitidine in Combination With Pembrolizumab and Epacadostat in Subjects With Advanced Solid Tumors and Previously Treated Stage IIIB or Stage IV Non-Small Cell Lung Cancer and Stage IV Microsatellite-Stable Colorectal Cancer (ECHO-206)

NCT02959437Registry updated 2025-10-21·Phase 1/Phase 2·INCY
Terminated

Primary endpoint: Part 1 and 2 : Number of Participants With Treatment Emergent Adverse Events

Interventionalopen70 targetStarted 2017-02Completion 2020-0312 sites · Spain, United Kingdom, United StatesIncyte Corporation

A Phase 1/2, Open-Label, Dose-Escalation/Dose-Expansion, Safety and Tolerability Study of INCB059872 in Subjects With Advanced Malignancies

NCT02712905Registry updated 2025-11-04·Phase 1/Phase 2·INCY
Terminated

Primary endpoint: Number of Participants Receiving INCB059872 Monotherapy With Any Treatment-emergent Adverse Event (TEAE)

Interventionalopen116 targetStarted 2016-05Completion 2022-0415 sites · Belgium, Netherlands, United StatesIncyte Corporation