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Study identifier: NCT05798897 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Non-Hodgkin Lymphoma, Adult · Non-Hodgkin Lymphoma, Refractory · Non-Hodgkin Lymphoma, Relapsed  ·  Sponsor: Marker Therapeutics, Inc.

PhasePhase 1
Planned participants79
Who can joinAll sexes, 18 Years to 100 Years
Healthy volunteersNo

About this study

This study is a Phase 1 multicenter study with a Dose Escalation and Dose Expansion evaluating safety and efficacy of MT-601 administration to patients with Relapsed or Refractory Lymphoma. The starting dose administered is 200 x 10\^6 cells (flat dosing).

This description comes directly from the study's public registry record.

Talk to the study team

Juan Vera, MD  ·  1 (713) 591-8100  ·  jvera@markertherapeutics.com

Patricia Allison  ·  1 (717) 471-5205  ·  pallison@markertherapeutics.com

Always discuss trial participation with your own doctor first.

Locations (7)

City of HopeDuarte, California, United StatesRecruiting
University of ColoradoAurora, Colorado, United StatesRecruiting
Colorado Blood Cancer Institute (Sarah Cannon)Denver, Colorado, United StatesRecruiting
University of Kansas Medical CenterKansas City, Kansas, United StatesRecruiting
CornellNew York, New York, United StatesRecruiting
Sarah Cannon Research Institute at St. David's South AustinAustin, Texas, United StatesRecruiting
University of Wisconsin Carbone Cancer CenterMadison, Wisconsin, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05798897