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.
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