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prmt5 inhibitor bgb-58067

Generic: PRMT5 Inhibitor BGB-58067

prmt5 inhibitor bgb-58067: 4 clinical trials tracked.

prmt5 inhibitor bgb-58067 evidence translation

What we can confirm

4 tracked trials

No verified listed developer

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 prmt5 inhibitor bgb-58067, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 1 study sponsors
Clinical Trials (4)

A Phase 1, Single Dose, Open-label, Randomized 4-Period, 4-Sequence Crossover Study to Assess the Relative Bioavailability of Two Tablet Formulations of BGB-58067 and the Effect of Food on the Pharmacokinetics of a Single Oral Dose of BGB-58067 Administered Simultaneously to Healthy Adult Participants

NCT07712640·Phase 1·ONC
Recruiting

Primary endpoint: Area under the Plasma Concentration-Time Curve from Time 0 Infinity (AUC0-inf) for BGB-58067

InterventionalRandomizedopen32 targetStarted 2026-07Completion 2028-071 site · AustraliaBeOne Medicines

An Open-Label, Parallel Group Study Designed to Investigate the Effect of the CYP3A Inducer Phenytoin and the CYP3A Inhibitor Itraconazole on the Pharmacokinetics of BGB-58067 in Healthy Participants

NCT07590102·Phase 1·ONC
Recruiting

Primary endpoint: Part A and Part B: Time of the Maximum Observed Concentration (Tmax) of BGB-58067

Interventionalopen30 targetStarted 2026-06Completion 2026-091 site · AustraliaBeOne Medicines

A Phase 0/2 Study of BGB-58067, an MTA Cooperative PRMT5 Inhibitor, in Newly Diagnosed Glioblastoma Patients With Methylthioadenosine Phosphorylase (MTAP) Deleted Tumors Scheduled for Resection to Evaluate Central Nervous System (CNS) Penetration With Pharmacodynamic (PD)-Triggered Expansion Cohorts

NCT07485049·Early Phase 1
Recruiting

Primary endpoint: Phase 0: Proportion of Participants with ≥ 50% Decrease from Baseline in SDMA Expression, or with SDMA H-Score ≤ 70, in Phase 0 Tumor Tissue Collected Intraoperatively

Interventionalopen78 targetStarted 2026-05Completion 2028-111 site · United StatesNader Sanai

A Phase 1a/b Study Investigating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Antitumor Activity of PRMT5 Inhibitor BGB-58067 Alone and in Combination With Anticancer Agents in Patients With Advanced Solid Tumors

NCT06589596·Phase 1·ONC
Recruiting

Primary endpoint: Phase 1a: Number of Participants with Adverse Events and Serious Adverse Events

Interventionalopen525 targetStarted 2025-01Completion 2027-0950 sites · Australia, Brazil, China, United StatesBeOne Medicines