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Completed Phase 1Phase 2 Interventional Results available

Study of ProTmune for Allogeneic HCT in Adult Patients With Hematologic Malignancies

ClinicalTrials.gov ID: NCT02743351

Public ClinicalTrials.gov record NCT02743351. 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 Nov 4, 2026, 2:55 AM EST

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Official title

A Phase 1, Non-Randomized, Open-Label/Phase 2, Randomized, Blinded Study of ProTmune™ (ex Vivo Programmed Mobilized Peripheral Blood Cells) Versus Non-Programmed Mobilized Peripheral Blood Cells for Allogeneic Hematopoietic Cell Transplantation in Adult Subjects With Hematologic Malignancies

Brief summary

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

This study is a Phase 1, non-randomized, open-label/Phase 2 randomized, blinded study of ProTmune (ex vivo programmed mobilized peripheral blood cells) versus non-programmed mobilized peripheral blood cells for allogeneic hematopoietic cell transplantation (HCT) in adult subjects aged 18 years and older with hematologic malignancies. A total of 88 study subjects were treated in the trial at approximately 15 centers in the US.

Study identification

NCT ID
NCT02743351
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Fate Therapeutics
Industry
Enrollment
96 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 20, 2016 (Actual)
Primary completion
Dec 4, 2020 (Actual)
Completion
Nov 5, 2021 (Actual)
Last update posted
Feb 8, 2023

2016 – 2021

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
University of Alabama Birmingham Alabama — —
City of Hope Duarte California 91010 —
University of California, San Diego (UCSD) Moores Cancer Center San Diego California — —
University of Chicago Chicago Illinois — —
Indiana Blood and Marrow Transplant Indianapolis Indiana 46237 —
Dana Farber Cancer Institute Boston Massachusetts 02215 —
Barbara Ann Karmanos Cancer Institute Detroit Michigan 48201 —
Weill Cornell Medicine New York New York — —
Jewish Hospital Cincinnati Ohio — —
The Ohio State University Columbus Ohio 43210 —
Oregon Health & Science University Portland Oregon — —
Sarah Cannon Research Institute Nashville Tennessee 37203 —
Texas Transplant Institute San Antonio Texas — —
Huntsman Cancer Institute (University of Utah) Salt Lake City Utah 84103 —
Virginia Commonwealth University Richmond Virginia 23298 —

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 NCT02743351, 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, 2023 · Synced Nov 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02743351 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →