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NCT Number: NCT06608732

Combination of Inaticabtagene Autoleucel With Autologous Hematopoietic Stem Cell Transplantation for Adolescents or Adults With MRD-Positive B-Cell Acute Lymphoblastic Leukemia in Initial Complete Remission.

Evaluate the safety and efficacy of Inaticabtagene autoleucel combined with autologous hematopoietic stem cell transplantation in adolescents or adults with MRD-positive initial complete remission in B-cell acute lymphoblastic leukemia.

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Key information

Age range

16 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

National Institute of Hematology, Chinese Academy of Medical Sciences

Tianjin, Tianjin Municipality, 300000, China

Location status: Recruiting

Location contact

erlie EL Jiang, Doctor

CONTACT

[email protected]

15122538106 ext. 022-23608602

About this study

Evaluate the safety and efficacy of Inaticabtagene autoleucel combined with autologous hematopoietic stem cell transplantation in adolescents or adults with MRD-positive initial complete remission in B-cell acute lymphoblastic leukemia.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ECOG score of 0 to 1
  • Newly diagnosed Ph-negative B-ALL within 6 months, achieving CR1 after standard induction chemotherapy, undergoing at least one consolidation therapy, and patients with bone marrow MRD ≥ 0.01% detected by routine flow cytometry.
  • Or newly diagnosed Ph-positive B-ALL within 6 months, achieving CR1 after guideline-recommended induction chemotherapy (or use of TKI), undergoing at least one consolidation therapy, and patients with BCR-ABL1 > 0% detected by routine q-PCR technology.
  • No significant organ dysfunction
  • Willing and meet the conditions for autologous hematopoietic stem cell transplantation

Exclusion criteria

  • Burkitt lymphoma/leukemia, heterozygous or double-expressor leukemia, or chronic myeloid leukemia in blast phase.
  • Before screening or pre-treatment, bone marrow or peripheral blood with blasts ≥ 5%; or extramedullary leukemia.
  • Individuals who have received CAR-T cell therapy before screening or pre-treatment; or patients who have undergone hematopoietic stem cell transplantation.
  • Patients with associated genetic syndromes related to bone marrow failure, such as Fanconi anemia, Kostmann syndrome, Shwachman syndrome, or any other known bone marrow failure syndromes.

Treatment and study plan

Inaticabtagene autoleucel

Biological

CNCT19 combined with autologous hematopoietic stem cell transplantation,Dose: (0.5 -2)x 10^6/kg CNCT19 Cell Injection via intravenous infusion.

Primary outcomes

  1. Relapse-Free Survival

    Time frame: From autologous hematopoietic stem cell transplantation to 2 years after transplantation

    The time from the start of infusion of Inaticabtagene autoleucel until the diagnosis of relapse or any death (whichever comes first).

Secondary outcomes

  1. Overall survival rate

    Time frame: From autologous hematopoietic stem cell transplantation to 2 years after transplantation

  2. Cumulative recurrence rate

    Time frame: From autologous hematopoietic stem cell transplantation to 2 years after transplantation

  3. MRD negativity rate

    Time frame: 28 days after the first CAR-T cell reinfusion

Sponsors and collaborators

Lead sponsor

Institute of Hematology & Blood Diseases Hospital, China

Other

Collaborators

  • Juventas Cell Therapy Ltd.

Registry information

Official study title

Clinical Study of Inaticabtagene Autoleucel Combined With Autologous Hematopoietic Stem Cell Transplantation for Adolescents or Adults With MRD-Positive B-Cell Acute Lymphoblastic Leukemia in Initial Complete Remission.

Important dates

Study start
2024
Primary completion
2028
Study completion
2028
First posted
Sep 23, 2024
Registry last updated
Nov 5, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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