Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Terminated Phase 1 Interventional

Natural Killer Cell (CYNK-001) Infusions in Adults with AML

ClinicalTrials.gov ID: NCT04310592

Public ClinicalTrials.gov record NCT04310592. 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 Oct 26, 2026, 3:43 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 Phase I Multi-dose Study of Human Placental Hematopoietic Stem Cell Derived Natural Killer Cells (CYNK-001) with or Without Recombinant Human Interleukin-2 (rhIL-2) in Adults with Primary or Secondary Acute Myeloid Leukemia (AML) in Morphologic Complete Remission with Minimal Residual Disease (MRD) or Relapsed/refractory (R/R) AML

Brief summary

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

This study will find the maximum tolerated dose or the maximum planned dose of CYNK-001 which contains natural killer (NK) cells derived from human placental CD34+ cells and culture-expanded. CYNK-001 cells will be given after lymphodepleting chemotherapy. The safety of this treatment will be evaluated, and researchers want to learn if NK cells will help in treating acute myeloid leukemia.

Study identification

NCT ID
NCT04310592
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Celularity Incorporated
Industry
Enrollment
27 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 Years
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
Mar 12, 2020 (Actual)
Primary completion
Jan 20, 2023 (Actual)
Completion
Apr 28, 2023 (Actual)
Last update posted
Dec 12, 2024

2020 – 2023

United States locations

U.S. sites
10
U.S. states
7
U.S. cities
9
Facility City State ZIP Site status
Colorado Blood Cancer Institute Denver Colorado 80218 —
University of Chicago Chicago Illinois 60637 —
Hackensack University Medical Center Hackensack New Jersey 07601 —
Roswell Park Comprehensive Cancer Center Buffalo New York 14203 —
Columbia University and New York Presbyterian Hospital New York New York 10032 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Westchester Medical Center Valhalla New York 10595 —
Tennessee Oncology Nashville Tennessee 37203 —
MD Anderson Cancer Center Houston Texas 77030 —
Swedish Health Services Seattle Washington 98122 —

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 NCT04310592, 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 Dec 12, 2024 · Synced Oct 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04310592 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →