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Terminated Phase 1 Interventional

Evaluate the Safety, Tolerability, Pharmacokinetic Profile, Efficacy of Bl-M11D1

ClinicalTrials.gov ID: NCT06714591

Public ClinicalTrials.gov record NCT06714591. 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 28, 2026, 3:02 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

A Multicenter, Open-Label Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Profile, and Preliminary Efficacy of BL-M11D1 in Patients With Relapsed/Refractory Acute Myeloid Leukemia.

Brief summary

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

The objective of this study to evaluate the safety, tolerability, pharmacokinetic profile, and preliminary efficacy of BL-M11D1 in patients with relapsed/refractory acute myeloid leukemia.

Study identification

NCT ID
NCT06714591
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
SystImmune Inc.
Industry
Enrollment
52 participants

Conditions and interventions

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
Dec 18, 2024
Primary completion
Sep 15, 2026
Completion
Sep 15, 2026
Last update posted
Sep 23, 2026

2024 – 2026

United States locations

U.S. sites
18
U.S. states
15
U.S. cities
18
Facility City State ZIP Site status
City of Hope Duarte California 91010 —
UCLA Ronald Reagan Medical Center Los Angeles California 90095 —
University of Colorado Anschutz Medical Campus Aurora Colorado 80045 —
Yale Cancer Center, Smilow Cancer Hospital at Yale New Haven New Haven Connecticut 06511 —
Moffitt Cancer Center Tampa Florida 33612 —
Northwestern Memorial Hospital Chicago Illinois 60611 —
The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Baltimore Maryland 21287 —
START Midwest/The Cancer and Hematology Center Grand Rapids Michigan 49546 —
John Theurer Cancer Center-Hackensack Hackensack New Jersey 07601 —
Oncology Hematology Care Clinical Trials, LLC Cincinnati Ohio 45236 —
The Ohio State University Comprehensive Cancer Center Columbus Ohio 43210 —
WVCI Oncology Associates of Oregon Eugene Oregon 24224 —
Oregon Health and Science University Portland Oregon 97239 —
Temple Health Fox Chase Cancer Center Philadelphia Pennsylvania 19111 —
SCRI -TriStar BMT Nashville Tennessee 37203 —
MD Anderson Cancer Center Houston Texas 77030 —
Virginia Cancer Specialists Fairfax Virginia 22031 —
Fred Hutchinson Cancer Center 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 NCT06714591, 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 Sep 23, 2026 · Synced Sep 28, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06714591 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →