A Study of CTD402 in T-ALL/LBL Patients

Recruiting Phase 1 Phase 2 Interventional Study
Acute Lymphocytic Leukemia Refractory Lymphoma, Lymphoblastic
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
12 and older
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
54 (estimated)
Sponsor
Imviva Bio · Industry
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About This Trial
The goal of the TENACITY-01 clinical trial is to learn if CTD402 UCART is safe and effective for relapsed/refractory T-ALL/LBL patients. Participants with relapsed/refractory T-ALL/LBL over the age of 12 will be eligible to participate. Participants will receive one infusion of CTD402 on Day 0 and will be evaluated for anti-tumor activity by an independent review committee based on the NCCN crit…
Trial Locations
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Eligibility Criteria
Key Inclusion Criteria: 1. Male or female, ≥ 12 years of age. 2. Participants with body weight ≥ 40 kilogram. 3. Relapsed or refractory T-ALL/LBL is defined as one of the following: 1. Relapsed or refractory disease after two or more lines of systemic therapy; 2. The first relapse occurs wit…
Contacts

Jan Davidson-Moncada, MD, PhD

917-573-8538

clinicaltrials@bioheng.com

CONTACT