A First-in-Human Study of BG-C0979 in Adults With Advanced Solid Tumors
← catalyst calendarNCT07414836 · readout in 985 d
Sponsored by BeOne Medicines (industry) · ONC — their whole pipeline →.
Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
84estimated
Sites
17
Countries
Australia, China, Spain +1
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| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-04-13 | actual | When the study began enrolling |
| Primary completion | 2029-04-30 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2029-04-30 | estimated | The whole study's end, after follow-up |
| First posted | 2026-02-17 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-08-06 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Advanced Solid Tumor
Interventions
- Drug: BG-C0979
- Drug: Tislelizumab — also filed as BGB-A317
Primary outcomes
what the primary-completion date above is the date OFPhase 1a: Number of Participants Experiencing Adverse Events (AEs)
measured Up to approximately 24 months
Phase 1a: Maximum Tolerated Dose (MTD) or Maximum Administered Dose (MAD) of BG-C0979 Monotherapy
measured Up to approximately 10 months
Phase 1a: Recommended Dose(s) for Expansion (RDFE[s])
measured Up to approximately 10 months
Phase 1b: Recommended Phase 2 Dose (RP2D)
measured Up to approximately 24 months
Phase 1b: Overall Response Rate (ORR)
measured Up to approximately 24 months
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