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Safety and Preliminary Efficacy of MT-601 in Patients With Relapsed/Refractory Lymphoma

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NCT05798897 · readout in 558 d

Sponsored by Marker Therapeutics, Inc. (industry) · MRKR — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
79estimated
Sites
7
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
Start2023-01-02actualWhen the study began enrolling
Primary completion2028-02-28estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-02-28estimatedThe whole study's end, after follow-up
First posted2023-04-05actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-08-20actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Non-Hodgkin Lymphoma, Adult
  • Non-Hodgkin Lymphoma, Refractory
  • Non-Hodgkin Lymphoma, Relapsed
  • Non Hodgkin Lymphoma
  • Hodgkin Lymphoma
  • Hodgkin Lymphoma, Adult
  • Hodgkin's Lymphoma, Relapsed, Adult

Intervention

  • Drug: MT-601

Primary outcomes

what the primary-completion date above is the date OF
Dose Escalation
measured After 3 or 6 patients in each dose cohort have been treated with MT-601 and have had the opportunity to be followed for 28 days.
Dose Expansion (ORR)
measured 12 months after the last patient treated in the Dose Expansion portion of the study receiving the first dose of MT-601.
Dose Expansion (DOR)
measured 12 months after the last patient treated in the Dose Expansion portion of the study receiving the first dose of MT-601.
Dose Expansion (CR)
measured 12 months after the last patient treated in the Dose Expansion portion of the study receiving the first dose of MT-601.

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