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Recruiting Phase 1 Interventional

An Investigational Study of BGB-58067 As a Single Agent and in Combination With Anticancer Agents in Participants With Advanced Solid Tumors

ClinicalTrials.gov ID: NCT06589596

Public ClinicalTrials.gov record NCT06589596. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 11, 2026, 8:12 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is an open-label, multicenter, first-in-human dose escalation and dose expansion study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary antitumor activity of BGB-58067 alone, in combination with BG-89894 (discontinued), and in combination with standard of care therapy in participants with advanced solid tumors and with methylthioadenosine phosphorylase (MTAP) deficiency.

Study identification

NCT ID
NCT06589596
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
BeOne Medicines
Industry
Enrollment
525 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 9, 2025
Primary completion
Sep 29, 2027
Completion
Sep 29, 2027
Last update posted
Jul 21, 2026

2025 – 2027

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
Usc Norris Comprehensive Cancer Center (Nccc) Los Angeles California 90089-1019 Recruiting
Adventhealth Celebration Florida 34747-4606 Recruiting
Dana Farber Cancer Institute Boston Massachusetts 02215-5418 Recruiting
Washington University School of Medicine St Louis Missouri 63110-1010 Recruiting
Nyu Langone Health New York New York 10016-2708 Recruiting
Columbia University Medical Center New York New York 10032 Recruiting
Sidney Kimmel Cancer Center Philadelphia Pennsylvania 19107-4307 Recruiting
Tennessee Oncology, Pllc Nashville Nashville Tennessee 37203 Recruiting
The University of Texas Md Anderson Cancer Center Houston Texas 77030-4009 Recruiting
Next Dallas Irving Texas 75039-2743 Recruiting
Next Virginia Fairfax Virginia 22031 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 87 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06589596, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 21, 2026 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06589596 live on ClinicalTrials.gov.

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