Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05703542

BXCL701 Phase 1 R/R Acute Myeloid Leukemia or Myelodysplastic Syndrome

A Phase 1 Study of BXCL701 in Relapsed/Refractory Acute Myeloid Leukemia or Relapsed/Refractory Myelodysplastic Syndrome With Excess Blasts - 2

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
24 (estimated)
Sponsor
Eric Stephen Winer, MD · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this research study is to find the safest and most effective dose of the study drug, BXCL701, for the treatment of Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome (MDS). The names of the study drugs involved in this study are/is: * BXCL701

Detailed description

This is a multi-center, single-arm, Phase I research study for the study drug, BXCL701, for participants with refractory or relapsed Acute Myeloid Leukemia (AML) and Myelodysplastic Syndrome with Excess Blasts-2 (MDS-EB-2). Phase I clinical trials test the safety and effectiveness of an investigational drug to learn whether the drug works in treating a specific disease. "Investigational" means the drug is being studied. BXCL701 is a synthetic dipeptide that is in tablet form and is taken by mouth. The U.S. Food and Drug Administration (FDA) has not approved BXCL701 as a treatment for any disease. Research study procedures include screening for eligibility and study treatment including evaluations, blood collections, bone marrow biopsies, and follow up visits. Participation in this study will last approximately 3 years. It is expected that about 24 people will participate in this study. BioXcel is supporting this research study by providing the study drug and funding research tests and procedures.

Conditions

Interventions

TypeNameDescription
DRUGBXCL701Tablet, taken Orally

Timeline

Start date
2023-02-02
Primary completion
2026-03-17
Completion
2026-07-31
First posted
2023-01-30
Last updated
2025-07-18

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05703542. Inclusion in this directory is not an endorsement.