Recruiting
Phase 1
Phase 2

CTD402

Sponsor:

Imviva Bio

Code:

NCT07070219

Conditions

Acute Lymphocytic Leukemia Refractory

Lymphoma, Lymphoblastic

Eligibility Criteria

Sex: All

Age: 1+

Healthy Volunteers: Not accepted

Interventions

CTD402 CAR T Cell Injection

Study Details

Brief summary:

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 1 year 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 criteria for T-ALL and the Lugano 2014 criteria for T-LBL.

Patients will be followed for up to 24 months in this study and will be required to enroll under a separate long term follow up protocol to be followed for up to 15 years.

Conditions

Acute Lymphocytic Leukemia Refractory

Lymphoma, Lymphoblastic

Study ID

NCT07070219

Start date

Oct 7, 2025

Status verified date

Aug, 2026

Completion date

Dec 30, 2028

Anticipated

Primary completion date

Sep 30, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 1+

Healthy Volunteers: Not accepted

Key Inclusion Criteria:

1. Male or female, ≥ 1 year of age.
2. Participants with body weight ≥ 40 kilogram.
3. A) Relapsed or refractory T-ALL/LBL or MRD positive defined as one of the following:

  • Relapsed or refractory disease after two or more lines of systemic therapy;
  • The first relapse occurs within 12 months after first remission;
  • Relapse after allogeneic HSCT and must be ≥100 days from HSCT prior to screening period.

B) Minimal Residual Disease (MRD) positive T-ALL/LBL is defined as evidence of MRD, defined as < 5% blasts in bone marrow but ≥ 1 cancer cell in 1,000 cells determined by NGS ClonoSEQ® and/or other regionally acceptable methodologies (e.g., EuroMRD guidelines).
4. The presence of bone marrow lymphoblasts is ≥ 5% as determined by morphologic evaluation or evidence of extramedullary disease at screening.
5. Adequate organ function
6. ECOG of 2 or less or Karnofsky PS ≥ 60 (for participants age ≥ 16) or Lansky PS ≥ 60 (for participants < 16) at screening.

Key Exclusion Criteria:

1. Participants with concomitant genetic syndromes associated with bone marrow failure states or any other known bone marrow failure syndrome.
2. Active central nervous system (CNS) involvement
3. Participants with following cardiac conditions will be excluded:

1. History of heart failure New York Heart Association (NYHA) class III or IV;
2. History of myocardial infarction, cardiovascular angioplasty or stenting, unstable angina, or other serious heart diseases within 12 months of enrollment.
4. Primary immune deficiency.
5. Presence of uncontrolled infections.
6. Known history of infection with the human immunodeficiency virus (HIV); hepatitis C virus and syphilis.
7. Active or latent hepatitis B virus infection
8. Epstein-Barr virus (EBV), Cytomegalovirus (CMV) DNA or IgM positive at screening.

Study Design

Enrollment

118 participants

Anticipated

Allocation

Non randomized

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: R/R T-ALL/LBL

experimental: T-ALL/LBL in remission but with minimal residual disease

Interventions

CTD402 CAR T Cell Injection

CAR T cells

Primary outcome measure

  • Safety Profile [ Time Frame: 24 months ]
  • Response Evaluation [ Time Frame: 24 months ]

Central Contacts and Locations

Central contacts

Jan Davidson-Moncada, MD, PhD

917-573-8538clinicaltrials@imvivabio.com

Locations

Stanford University

Recruiting

Palo Alto, California, United States, 94304

Contacts

University of Chicago

Recruiting

Chicago, Illinois, United States, 60637

Mayo Clinic - Rochester

Recruiting

Rochester, Minnesota, United States, 55905

Memorial Sloan Kettering Cancer Center

Recruiting

New York, New York, United States, 11101

Montefiore Einstein Comprehensive Cancer Center

Recruiting

The Bronx, New York, United States, 10467

Sarah Cannon Research Insitute

Recruiting

Nashville, Tennessee, United States, 37203

Contacts

Haydar Frangoul, MD

844-482-4812

MD Anderson Cancer Center

Recruiting

Houston, Texas, United States, 77030

Contacts

Nitin Jain, MD

njain@mdanderson.org

More Information

Sponsor

Imviva Bio

Last update posted

Aug 19, 2026

Last verified

Aug, 2026

Keywords

  • CAR-T Therapy
  • relapsed/refractory

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Imviva Bio on 2026-08-19.