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Study details
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A Study of TSC-100 and TSC-101 in AML, ALL and MDS in Patients Undergoing Allogeneic Peripheral Blood Stem Transplantation

TScan Therapeutics, Inc.
NCT IDNCT05473910ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

75

Study length

about 3.7 years

Ages

18+

Locations

15 sites in CA, CT, FL +10

What this study is about

Researchers are testing whether TSC-100 or TSC-101 are safe and effective when given to people with Acute Myeloid Leukemia (AML), Acute Lymphoblastic Leukemia (ALL), or Myelodysplastic Syndromes (MDS) who are receiving a stem cell transplant from a donor. The trial will involve different doses of TSC-100 or TSC-101, along with standard treatment.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Control
  • 2.Take SOC + TSC-100
  • 3.Take SOC + TSC-101

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Occurrence of adverse events

Secondary: Comparison of disease free survival in patients versus the control arm, Comparison of overall survival between patients and control arm, Disease-free survival in patients versus the control arm at 18 months, defined as the time from date of transplant to death or relapse/progression, whichever comes first. Participants alive and disease free will be censored at the last follow-up.

Body systems

Oncology