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NCT06695507 · ClinicalTrials.gov registry record · Phase 1

Upfront Ruxolitinib for Chronic Graft-vs-host Disease

A Phase 1 study, sponsored by Children's Hospital Medical Center, Cincinnati.

Terminated
Registry status
Phase 1
Development phase
1
Enrollment target

NCT06695507: Clinical Trial Phase 1 study, sponsored by Children's Hospital Medical Center, Cincinnati.

NCT06695507 is a Phase 1 study that was terminated before completion, run by Children's Hospital Medical Center, Cincinnati. 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

NCT06695507, a Phase 1 study, was terminated before completion, sponsored by Children's Hospital Medical Center, Cincinnati.

TERMINATED
Registry status
Phase 1
Development phase
1 participants
Enrollment target

Study Summary

While hematopoietic stem cell transplant (HSCT) is an effective therapy, graft versus host disease (GVHD) is the most significant complication after HSCT. Corticosteroids (or steroids) have been the mainstay of treatment for chronic GVHD for many decades now. Increasingly, newer immunosuppressive and immunomodulating agents are being studied in adults and children affected by cGVHD. Ruxolitinib is one of these promising newer agents, which has been shown to be effective in the treatment of cGVHD in both children and adults. Currently, ruxolitinib is generally added to a patient's treatment regimen after (or with) a course of high dose steroids. The purpose of this study is to examine the effectiveness of upfront single agent ruxolitinib for cGVHD.

Interventions

  • DRUG Ruxolitinib

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2025-02-19
Est. Completion 2025-09-18
Phase Phase 1

Why NCT06695507 stopped before completion

NCT06695507 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 Ruxolitinib is the first listed.

NCT06695507 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06695507 about?

NCT06695507 is a clinical study titled "Upfront Ruxolitinib for Chronic Graft-vs-host Disease". While hematopoietic stem cell transplant (HSCT) is an effective therapy, graft versus host disease (GVHD) is the most significant complication after HSCT. Corticosteroids (or steroids) have been the mainstay of treatment for chronic GVHD for many decades now. Increasingly, newer immunosuppressive an...

What is the current status of trial NCT06695507?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 1 participants. The study started on 2025-02-19. Estimated completion is 2025-09-18.

What interventions are being tested in trial NCT06695507?

The interventions under investigation include: Ruxolitinib (DRUG).

Who is sponsoring clinical trial NCT06695507?

This trial is sponsored by Children's Hospital Medical Center, Cincinnati, which has 571 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06695507'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 NCT06695507, the US trial registry maintained by the National Library of Medicine. NCT06695507 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.