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Terminated Phase 1 Interventional

First-in-Human Study of FLX925 in Subjects With Relapsed or Refractory Acute Myeloid Leukemia

ClinicalTrials.gov ID: NCT02335814

Public ClinicalTrials.gov record NCT02335814. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 4:39 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 1/1b, First-in-Human, Dose-Escalation and Expansion Study of FLX925 Administered Orally to Subjects With Relapsed or Refractory Acute Myeloid Leukemia

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This first-in-human (FIH) clinical trial is a Phase 1/1b, open-label, sequential-group, dose-escalation and cohort expansion study evaluating the safety, PK, PD, and antitumor activity of FLX925 in subjects with relapsed or refractory AML.

Study identification

NCT ID
NCT02335814
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
RAPT Therapeutics, Inc.
Industry
Enrollment
51 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 7, 2015
Primary completion
May 2, 2017
Completion
May 2, 2017
Last update posted
Feb 8, 2018

2015 – 2017

United States locations

U.S. sites
12
U.S. states
12
U.S. cities
12
Facility City State ZIP Site status
Mayo Clinic Scottsdale Arizona 85259
University of Colorado Cancer Center Aurora Colorado 80045
Mayo Clinic Cancer Center Jacksonville Florida 32224
Northwestern University, Robert H. Lurie Comprehensive Cancer Center Chicago Illinois 60611
University of Michigan Ann Arbor Michigan 48109
Mayo Clinic Rochester Minnesota 55905
Memorial Sloan Kettering Cancer Center New York New York 10065
Duke Cancer Center Durham North Carolina 27710
University of Pennsylvania, Abramson Cancer Center Philadelphia Pennsylvania 19104
MD Anderson Cancer Center Houston Texas 77030
Huntsman Cancer Institute Salt Lake City Utah 84112
University of Washington/Seattle Cancer Care Alliance Seattle Washington 98109

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02335814, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 8, 2018 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02335814 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →