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NCT06462365RecruitingPhase 1

Prevention of GvHD in Participants With Hematological Malignancies Undergoing Hematopoietic Stem Cell Transplant (HSCT)

Phase I, First in Human, Open Label Study to Evaluate Safety and Tolerability of TRX103 Cells in Subjects With Hematological Malignancies Undergoing HLA-mismatched Related or Unrelated Hematopoietic Stem Cell Transplantation (HSCT)

Source: ClinicalTrials.gov · Last updated 15 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The purpose of this Phase 1, first in human open-label study is to assess the safety and tolerability of TRX-103 in patients with hematological malignancies undergoing HLA-mismatched related or unrelated hematopoietic stem cell transplantation (HSCT). It is anticipated that up to 36 Subjects will be enrolled during a 18-24 month enrollment period. TRX-103 will be infused one time post HSCT.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
36 (estimated)
First submitted
6 Jun 2024
Start date
8 Apr 2024
Primary completion date
15 Apr 2026
Lead sponsor
Tr1X, Inc.
NCT number
NCT06462365

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 36
  • From 8 Apr 2024 to the primary completion date, 15 Apr 2026
  • 5 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior allogeneic bone marrow, peripheral blood, or cord blood HSCT.
  • Positive hepatitis-C antibody with positive Recombinant Immunoblot Assay (RIBA) or PCR unless the subject has received curative anti-viral treatment and confirmed negative viral load by PCR.
  • Received another investigational agent for treatment of disease understudy within 28 days (or 5 half-lives, whichever is shorter) of conditioning and/or have not recovered from treatment related toxicities.
  • Subjects with a previous history of Thrombotic Thrombocytopenic Purpura (TTP) or Hemolytic Uremic Syndrome (HUS) who are not good candidates for treatment with sirolimus.

Other illness

  • Any subject with a history of significant renal, hepatic, pulmonary, or cardiac dysfunction, or on treatment to support cardiac dysfunction.
  • HIV positive.
  • Positive hepatitis-B surface antigen. Subject may be included if they are HBV PCR negative.

Lab values

  • Any serious illness, uncontrolled inter-current illness, psychiatric illness, active or uncontrolled infection, or other medical condition or history, including laboratory results.

Other

  • Subjects that are pregnant, breast feeding or aim to become pregnant during the study period. (Subjects must agree to use a highly effective method of contraception).

Who the study is looking for

  • Subjects with one of the following hematologic malignancies: Acute Lymphoblastic Leukemia (B- or T-ALL), Acute Myeloid Leukemia (AML) and Myelodysplastic Syndrome (MDS), or Chronic myelomonocytic leukemia (CMML)
  • Males and Females Age ≥ 18 years.
  • Weight of ≥ 35 Kg.
  • Karnofsky performance status ≥ 70 %.
  • Available mismatched related (haploidentical) or unrelated donors for peripheral blood stem cell (PBSC) donation.
  • Subjects must otherwise fulfill institutional criteria for eligibility to undergo allogeneic stem cell transplantation.
  • Absence of uncontrolled bacterial, viral or fungal infection at time of enrollment.
  • Have adequate organ function.
  • Subjects \> 65-year-old receiving MAC conditioning will only be eligible if they have a HSCT-comorbidity index score \< 5.
  • Subjects must be able to understand and sign informed consent and be willing and able to complete all specified procedures and visits.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (5)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Dana-Farber Cancer Institute
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting
City of Hope
Coordinator of this site? Confirm its status
DuarteUnited StatesRecruiting
University of Minnesota
Coordinator of this site? Confirm its status
MinneapolisUnited StatesRecruiting
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Fred Hutchinson Cancer Center
Coordinator of this site? Confirm its status
SeattleUnited StatesRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.