Phase I Trial of Targeted Immunotherapy with Daratumumab Following Myeloablative TBI-Based Conditioning and AlloHCT in Children, Adolescents and Young Adults with High Risk T-Cell Acute Lymphoblastic Leukemia and Lymphoma (ALLO-T-DART)

Who is this study for? Children, adolescents and young adults with high risk T-cell acute lymphoblastic leukemia and lymphoma
What treatments are being studied? Daratumumab
Status: Recruiting
Location: See all (16) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

A Phase I trial to determine the safety of targeted immunotherapy with daratumumab (DARA) IV after total body irradiation (TBI)-based myeloablative conditioning and allogeneic hematopoietic cell transplantation (HCT) for children, adolescents, and young adults (CAYA) with high risk T-cell acute lymphoblastic leukemia (T-ALL) or T-cell lymphoblastic lymphoma (T-LLy). Pre- and post-HCT NGS-MRD studies will be correlated with outcomes in children, adolescents, and young adults with T-ALL undergoing allogeneic HCT and post-HCT DARA treatment. The study will also evaluate T-cell repertoire and immune reconstitution prior to and following DARA post-HCT treatment and correlate with patient outcomes.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 39
Healthy Volunteers: f
View:

• 0-39yrs

• T-cell ALL in second or subsequent remission (≤ 5% blasts) or relapsed T-cell LLy with complete response after re-induction therapy (including secondary malignancy)

• Planned allogeneic stem cell transplantation with donor identified

• Performance status ≥ 60%

• Fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study

• Meet organ function requirements

• Signed IRB approved informed consent

Locations
United States
Arizona
Phoenix Children's Hospital
NOT_YET_RECRUITING
Phoeniz
California
Loma Linda University Children's Hospital
RECRUITING
Loma Linda
University of California
NOT_YET_RECRUITING
Los Angeles
University of California
NOT_YET_RECRUITING
San Francisco
Colorado
Children's Hospital Colordao
NOT_YET_RECRUITING
Aurora
Washington, D.c.
Children's National Medical Center
NOT_YET_RECRUITING
Washington D.c.
Florida
University of Florida
RECRUITING
Gainsville
John Hopkins All Children's Hospital
NOT_YET_RECRUITING
St. Petersburg
Indiana
Riley Children's Hospital
RECRUITING
Indianapolis
Massachusetts
Boston Children's Hospital
NOT_YET_RECRUITING
Boston
Michigan
Helen DeVos Children's Hospital
RECRUITING
Grand Rapids
New York
New York Medical College
RECRUITING
Vallhala
Ohio
Nationwide Children's Hosptial
NOT_YET_RECRUITING
Columbus
Pennsylvania
Children's Hospital of Philadelphia
RECRUITING
Philadelphia
Texas
MD Anderson Cancer Center
NOT_YET_RECRUITING
Houston
Wisconsin
Medical College of Wisconsin
NOT_YET_RECRUITING
Milwaukee
Contact Information
Primary
Lauren Harrison, RN, MSN
lauren_harrison@nymc.edu
6172857844
Backup
Erin Morris, RN
erin_morris@nymc.edu
7149645359
Time Frame
Start Date: 2023-05-22
Estimated Completion Date: 2028-09
Participants
Target number of participants: 30
Treatments
Other: Interventional
Phase 1: 3 dose levels to determine safety (15 patients)~Dose expansion:~Daratumumab (DARA) treatment post-HCT~1. Induction: DARA IV weekly x 8 doses (Weeks 1-8)~2. Consolidation: DARA IV every 2 weeks x 8 doses (Weeks 9-24)~3. Maintenance: DARA IV every 4 weeks (Stop at Day +270)
Sponsors
Leads: New York Medical College

This content was sourced from clinicaltrials.gov

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