Safety and Preliminary Efficacy of MT-601 in Patients With Relapsed/Refractory Lymphoma
A Phase 1 Study of Patient-Derived Multi-Tumor-Associated Antigen-Specific T Cells (MT-601) Administered to Patients With Relapsed or Refractory Non-Hodgkin and Hodgkin Lymphoma (APOLLO)
Marker Therapeutics, Inc.
79 participants
Jan 2, 2023
INTERVENTIONAL
Conditions
Summary
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).
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
Multi-antigen specific CD4+ andCD8+ T cells
Locations(7)
View Full Details on ClinicalTrials.gov
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NCT05798897