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A Study of CLN-619 (Anti-MICA/MICB Antibody) in Patients With Relapsed and Refractory Multiple Myeloma

← catalyst calendar

NCT06381141 · readout ≤ 42 d

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

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
30estimated
Sites
8
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

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-09-03actualWhen the study began enrolling
Primary completionSep 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionMar 2027estimatedThe whole study's end, after follow-up
First posted2024-04-24actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-09-18actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Multiple Myeloma

Intervention

  • Drug: CLN-619

Primary outcomes

what the primary-completion date above is the date OF
Proportion of participants reporting Adverse Events (AEs) and Serious Adverse Events (SAEs)
measured baseline through 3-week treatment period
Changes in Eastern Cooperative Oncology Group (ECOG) performance
measured Up to 2 years
Incidence of Dose-Limiting toxicity (DLTs)
measured up to 2 years
Best Overall Response (BOR) per patient
measured up to 2 years
Overall Response Rate (ORR)
measured up to 2 years
Duration of Response (DoR)
measured up to 2 years
Clinical Benefit Rate (CBR)
measured up to 2 years
Progression Free Survival (PFS)
measured up to 2 years
Overall Survival (OS)
measured up to 2 years

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