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A Study of TRK-950 in Patients With Advanced Solid Tumors

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NCT05423262 · readout ≤ 499 d

Sponsored by Toray Industries, Inc (industry) · 3402.T — their whole pipeline →.

Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
49estimated
Sites
10
Country
Japan

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
Start2022-07-06actualWhen the study began enrolling
Primary completionDec 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionDec 2027estimatedThe whole study's end, after follow-up
First posted2022-06-21actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-13actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Solid Tumor
  • Melanoma

Interventions

  • Biological: TRK-950
  • Biological: TRK-950
  • Biological: TRK-950
  • Drug: Nivolumab
  • Biological: TRK-950

Primary outcomes

what the primary-completion date above is the date OF
Number of participants with dose-limiting toxicities (DLTs) (Part 1 and 2)
measured Up to Day 28
Number of participants with adverse events (AEs) (Part 1 and 2)
measured through study completion, an average of 1 year
Number of participants with adverse events of special interest (AESIs) (Part 1 and 2)
measured through study completion, an average of 1 year
Number of participants with serious adverse events (SAEs) (Part 1 and 2)
measured through study completion, an average of 1 year
Objective response rate (ORR) (Part 3)
measured Up to approximately 12 months

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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