A Phase 1 Study to Evaluate the Safety and Tolerability of a Combination Autologous CD19 CAR T Cell Therapy (SYNCAR-001 + STK-009) in Subjects With Relapsed or Refractory CD19+ Hematologic Malignancies (Leukemia)
Study of STK-009 in Combination with SYNCAR-001 in Patients with Lymphoma or Leukemia
Sponsor: Synthekine, Inc.
Enrolling: Male and Female Patients
IRB Number: AAAU3113
U.S. Govt. ID: NCT05665062
Contact: Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu
Additional Study Information: The purpose of this study is to find the highest dose of STK-009 that is safe in combination with a dose of SYNCAR-001 and to learn what side effects are experienced in people with certain lymphomas or leukemias. This study will also evaluate how much SYNCAR-001 and STK-009 is in your blood at various times, whether your immune system becomes activated, whether your body produces antibodies (proteins produced by your immune system) against SYNCAR-001 and/or STK-009, and the effects of SYNCAR-001 + STK-009 on your cancer.
This study is closed
Investigator
Ran Reshef, MD
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For more information, please contact:
Research Nurse Navigator
cancerclinicaltrials@cumc.columbia.edu
212-342-5162
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