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CLN-617 Alone and in Combination With Pembrolizumab in Patients With Advanced Solid Tumors

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NCT06035744

Sponsored by Cullinan Therapeutics Inc. (industry) · CGEM — their whole pipeline →.

Phase
Phase 1
Status
Terminated
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
23actual
Sites
5
Country
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

Why the sponsor stopped it

Company decision

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
Start2023-12-12actualWhen the study began enrolling
Primary completion2026-06-16actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-06-16actualThe whole study's end, after follow-up
First posted2023-09-13actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-18actualThe 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: CLN-617
  • Drug: Pembrolizumab — also filed as Keytruda

Primary outcomes

what the primary-completion date above is the date OF
Dose Escalation
measured 24 Months
Dose Optimization
measured 24 Months
Dose Expansion
measured 24 Months
Dose Expansion
measured 24 Months
Dose Expansion
measured 24 Months
Dose Expansion
measured 24 Months
Dose Expansion
measured 24 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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