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NCT02354443 · ClinicalTrials.gov registry record · Phase 1

A Trial of a Single ProHema-CB Product Transplant in Pediatric Patients With Inherited Metabolic Disorders

A Phase 1 study, sponsored by Fate Therapeutics.

Terminated
Registry status
Phase 1
Development phase
1
Enrollment target

NCT02354443: Clinical Trial Phase 1 study, sponsored by Fate Therapeutics.

NCT02354443 is a Phase 1 study that was terminated before completion, run by Fate Therapeutics. The registered enrollment target is 1 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02354443, a Phase 1 study, was terminated before completion, sponsored by Fate Therapeutics.

TERMINATED
Registry status
Phase 1
Development phase
1 participants
Enrollment target

Study Summary

The purpose of this study is to describe the safety profile of ProHema-CB as part of a single cord blood unit transplant after a myeloablative conditioning regimen in pediatric patients with inherited metabolic disorders. The safety profile will primarily be assessed by neutrophil engraftment.

Interventions

  • BIOLOGICAL ProHema-CB Transplant

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2015-06
Est. Completion 2017-02
Phase Phase 1
Fate Therapeutics

22 total trials

Why NCT02354443 stopped before completion

NCT02354443 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 1 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which ProHema-CB Transplant is the first listed.

NCT02354443 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02354443 about?

NCT02354443 is a clinical study titled "A Trial of a Single ProHema-CB Product Transplant in Pediatric Patients With Inherited Metabolic Disorders". The purpose of this study is to describe the safety profile of ProHema-CB as part of a single cord blood unit transplant after a myeloablative conditioning regimen in pediatric patients with inherited metabolic disorders. The safety profile will primarily be assessed by neutrophil engraftment.

What is the current status of trial NCT02354443?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 1 participants. The study started on 2015-06. Estimated completion is 2017-02.

What interventions are being tested in trial NCT02354443?

The interventions under investigation include: ProHema-CB Transplant (BIOLOGICAL).

Who is sponsoring clinical trial NCT02354443?

This trial is sponsored by Fate Therapeutics, which has 22 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02354443's enrollment target sits among peer trials

1 2001st of 2000 the lowest 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 NCT02354443, the US trial registry maintained by the National Library of Medicine. NCT02354443 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.