Forecasting Relapse Outcomes With AlloHeme-based Risk Detection in Post-Allo-HCT AML/MDS Patients (FORWARD)

Study acronym: FORWARD
StatusEnrolling by Invitation
PhaseNot specified
SponsorCareDx
Started

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Record History

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  1. Notable Enrolling by invitation only Show 5 more changesShow less
    • Primary endpoints: details revised at 1 of 1 entry
    • Study sites: 1 to 3
    • Start date changed from estimate of Aug 31, 2026 to Sep 24, 2026
    • Eligibility criteria expanded, about 15 words
    • Secondary endpoints: details revised at 2 of 5 entries
  2. Minor Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
6 trials monitored
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2,957 trials monitored
See 176 trials at risk
and 1 more disease
AlloHeme is a blood-based monitoring test developed by the CareDx laboratory that utilizes NGS technology coupled with a proprietary algorithm to predict the likelihood of a relapse in post-allo-HCT AML/MDS patients. The technology analyzes 405 single nucleotide polymorphisms (SNPs) selected from across all somatic chromosomes between the donor and the recipient. Pre-transplant DNA is obtained from donor and/or recipient to identify specific donor and recipient SNPs (baseline samples). Post-transplant blood samples are obtained and compared to the baseline sample profiles to precisely calculate the percentage chimerism of recipient cells in the blood samples using a proprietary quantitative method and unique dual indexing that optimizes recipient DNA at trace levels. This approach enables highly accurate and reproducible chimerism measurement with a limit of detection down to 0.02%. The AlloHeme test leverages a proprietary algorithm that integrates this multi-analyte longitudinal chimerism data with post-transplant time points to predict the likelihood of a clinical relapse for AML/MDS patients following an allo-HCT.
Trial Details
NCT Number NCT07607327
Lead Sponsor CareDx
Conditions
(from sponsor)
AML (Acute Myelogenous Leukemia), MDS (Myelodysplastic Syndrome), CMML
Related terms Anemia, Refractory, with Excess of Blasts, Leukemia, Myeloid, Acute, Recurrence
Enrollment 400 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov