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A Study of BG-C477 in Participants With Advanced Solid Tumors

← catalyst calendar

NCT06596473 · readout in 499 d

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

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
310estimated
Sites
58
Countries
Australia, China, Japan +5

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

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-10-03actualWhen the study began enrolling
Primary completion2027-12-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-12-31estimatedThe whole study's end, after follow-up
First posted2024-09-19actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-03actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Advanced Solid Tumors

Interventions

  • Drug: BG-C477
  • Drug: Tislelizumab — also filed as BGB-A317
  • Drug: Chemotherapy

Primary outcomes

what the primary-completion date above is the date OF
Phase 1a: Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)
measured From first dose of the study drug(s) to 30 days after the last dose (up to approximately 2 years)
Phase 1a: Maximum Tolerated Dose (MTD) or Maximum Administered Dose (MAD)
measured Approximately 1 year
Phase 1a: Recommended Dose(s) for Expansion (RDFE[s]) of BG-C477
measured Approximately 1 year
Phase 1b: Overall Response Rate (ORR)
measured Approximately 2 years
Phase 1b: Recommended Phase 2 Dose (RP2D) of BG-C477
measured Approximately 2 years

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