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NCT04310592 · ClinicalTrials.gov registry record · Phase 1

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

A Phase 1 study, sponsored by Celularity Incorporated.

Terminated
Registry status
Phase 1
Development phase
27
Enrollment target

NCT04310592: Clinical Trial Phase 1 study, sponsored by Celularity Incorporated.

NCT04310592 is a Phase 1 study that was terminated before completion, run by Celularity Incorporated. The registered enrollment target is 27 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04310592, a Phase 1 study, was terminated before completion, sponsored by Celularity Incorporated.

TERMINATED
Registry status
Phase 1
Development phase
27 participants
Enrollment target

Study Summary

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.

Primary Outcome

The number of participants who experience a DLT will be measured.

Interventions

  • BIOLOGICAL CYNK-001

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2020-03-12
Est. Completion 2023-04-28
Phase Phase 1
Celularity Incorporated

14 total trials

Why NCT04310592 stopped before completion

NCT04310592 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower).

The record links to 0 conditions, and to 1 intervention - of which CYNK-001 is the first listed.

NCT04310592 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04310592 about?

NCT04310592 is a clinical study titled "Natural Killer Cell (CYNK-001) Infusions in Adults with AML". 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 evalua...

What is the current status of trial NCT04310592?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 27 participants. The study started on 2020-03-12. Estimated completion is 2023-04-28.

What interventions are being tested in trial NCT04310592?

The interventions under investigation include: CYNK-001 (BIOLOGICAL).

Who is sponsoring clinical trial NCT04310592?

This trial is sponsored by Celularity Incorporated, which has 14 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04310592's enrollment target sits among peer trials

27 1463rd of 2000 higher than 519 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04310592, the US trial registry maintained by the National Library of Medicine. NCT04310592 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.