Phase 1/1b Study of T-allo10 Infusion After HLA-Partially Matched Related or Unrelated TCR αβ+ T-cell/ CD19+ B-cell Depleted Allogeneic Hematopoietic Stem Cell Transplantation (αβ Depleted-HSCT) in Children and Young Adults Affected by Hematologic Malignancies

Status: Recruiting
Location: See location...
Intervention Type: Biological, Drug, Device
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

The purpose of this study is to determine the safety of a cell therapy, T-allo10, after αβdepleted-HSCT in the hopes that it will boost the adaptive immune reconstitution of the patient while sparing the risk of developing severe Graft-versus-Host Disease (GvHD). The primary objective of Phase 1a is to determine the recommended Phase 2 dose (RP2D) administered after infusion of αβdepleted-HSCT in children and young adults with hematologic malignancies. A Phase 1b extension will occur after dose escalation, enrolling at the RP2D for the T-allo10 cells determined in the Phase 1 portion to evaluate the safety and efficacy of infusion of T-allo10 after receipt of αβdepleted-HSCT. Additionally, Phase 1b aims to explore improvements in immune reconstitution. All participants on this study must be enrolled on another study: NCT04249830

Eligibility
Participation Requirements
Sex: All
Minimum Age: 1 month
Maximum Age: 45
Healthy Volunteers: f
View:

• 1\. Age \> 1 months (with minimum weight of 10 Kg) and \< 45 years.

• 2\. Patients deemed eligible for allogeneic HSCT under the originating study, NCT 04249830

• 3\. Patients with life-threatening hematological malignancies for which HSCT has been recommended:

∙ High-risk ALL in 1st CR, ALL in 2nd or subsequent CR;

‣ High-risk AML in 1st CR, AML in 2nd or subsequent CR;

‣ Myelodysplastic syndrome;

‣ JMML (Juvenile myelomonocytic leukemia);

‣ Non-Hodgkin lymphomas in 2nd or subsequent CR;

‣ Other hematologic malignancies eligible for stem cell transplantation per institutional standard.

• 4\. All subjects ≥ 18 years of age must be able to give informed consent, or adults lacking capacity to consent must have a LAR available to provide consent. For subjects \<18 years old their LAR (i.e. parent or guardian) must give informed consent. Pediatric subjects will be included in age appropriate discussion and verbal assent will be obtained for those \> 7 years of age, when appropriate.

⁃ Patient already received αβdepleted-HSCT and has myeloid engraftment.

⁃ Absence of active grade II aGvHD requiring \>0.5 mg/Kg of steroids or any diagnosis of grade III/IVaGvHD.

Locations
United States
California
Lucile Packard Children's Hospital
RECRUITING
Palo Alto
Time Frame
Start Date: 2021-02-10
Estimated Completion Date: 2029-03
Participants
Target number of participants: 22
Treatments
Experimental: Cohort 1
The participant will undergo a alpha-beta depleted stem cell transplant using donor cells. The participant's cells will then be manipulated via a T-allo10 cell addback to reach a dose level of 1 X 10\^5/kg
Experimental: Cohort 2
The participant will undergo a alpha-beta depleted stem cell transplant using donor cells. The participant's cells will then be manipulated via a T-allo10 cell addback to reach a dose level of 3 X 10\^5/kg
Experimental: Cohort 3
The participant will undergo a alpha-beta depleted stem cell transplant using donor cells. The participant's cells will then be manipulated via a T-allo10 cell addback to reach a dose level of 1 X 10\^6/kg
Sponsors
Leads: Porteus, Matthew, MD
Collaborators: California Institute for Regenerative Medicine (CIRM)

This content was sourced from clinicaltrials.gov

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