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Study of GS-0201 Alone and in Combination in Participants With Advanced Solid Tumors

← catalyst calendar

NCT06167317 · readout ≤ 773 d

Sponsored by Gilead Sciences (industry) · GILD — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
278estimated
Sites
8
Countries
Israel, United States

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
Start2024-01-09actualWhen the study began enrolling
Primary completionSep 2028estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionSep 2028estimatedThe whole study's end, after follow-up
First posted2023-12-12actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-13actualThe 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: GS-0201
  • Drug: Sacituzumab Govitecan — also filed as IMMU-132, Trodelvy™, GS-0132

Primary outcomes

what the primary-completion date above is the date OF
The Number of Participants with Dose Limiting Toxicities (DLTs) During Dose Escalation
measured First dose up to 30 days post last dose (Up to approximately 109 weeks).
The Percentage of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)
measured First dose up to 30 days post last dose (Up to approximately 109 weeks).
The Incidence of Laboratory Abnormalities
measured First dose up to 30 days post last dose (Up to approximately 109 weeks).

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