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A Study of BGB-R046 as Monotherapy and in Combination With Tislelizumab in Solid Tumors

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NCT06487858

Sponsored by BeOne Medicines (industry) · ONC — their whole pipeline →.

Phase
Phase 1
Status
Terminated
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
42actual
Sites
8
Country
China

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Why the sponsor stopped it

This decision is due to a company business decision with a strategy change on the BGB-R046 development in Advanced or Metastatic Solid Tumors.

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-07-16actualWhen the study began enrolling
Primary completion2026-04-09actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-04-09actualThe whole study's end, after follow-up
First posted2024-07-05actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-11actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Solid Tumor

Interventions

  • Drug: BGB-R046
  • Drug: Tislelizumab

Primary outcomes

what the primary-completion date above is the date OF
Phase 1a: Number of Participant with Adverse Events, Serious Adverse Events, Adverse Events of Clinical Interest and Dose-limiting Toxicities
measured Up to approximately 2 years
Phase 1a: Maximum Tolerated Dose (MTD) or Maximum Administered Dose (MAD) of BGB-R046
measured Up to approximately 2 years
Phase 1a: Recommended Dose(s) for Expansion (RDFE[s]) of BGB-R046
measured Up to approximately 2 years
Phase 1b: Overall Response Rate (ORR)
measured Up to approximately 2 years

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