A Clinical Study of CHT101 in CD70-Positive Relapsed or Refractory Hematological Malignancies

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-70
SponsorTianjin Medical University Cancer Institute and Hospital

About this trial

Evaluate the Safety, Pharmacokinetics and Efficacy of CHT101 in Subjects With Relapsed or Refractory T or B Cell Hematological Malignancies

Eligibility criteria

Qualifiers

Willing and able to provide written informed consent.

Aged 18 to 70 years, male or female.

Confirmed CD70 positive in tumor tissue by immunohistochemistry (IHC).

Peripheral T cell lymphoma (including peripheral T cell lymphoma NOS, angioimmunoblastic T cell lymphoma, anaplastic large cell lymphoma, etc.) who have failed ≥1 line of systemic therapy.

Disqualifiers

History or presence of CNS metastasis, or clinically relevant CNS pathology such as seizure, stroke, severe brain injury, etc.

History of solid organ transplantation.

Prior treatment with CD70-targeting agents.

Prior treatment with CAR-T or other cellular/gene therapies.

Trial design

Treatments tested in this trial

  • CHT101

Treatment groups

24 Participants
are divided into 1 treatment group

Sponsors and collaborators

Tianjin Medical University Cancer Institute and Hospital

Lead sponsor

Nanjing Calmhome Cell and Gene Engineering Institute Co., Ltd.

Collaborator