JAKAVI under the microscope: new study tracks GVHD treatment in real life
NCT ID NCT07594587
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is tracking the safety and effectiveness of the drug JAKAVI (ruxolitinib) in 395 patients with graft-versus-host disease (GVHD), a complication of bone marrow transplants. Researchers are monitoring infections and other side effects in patients receiving the drug in routine clinical care. The goal is to see how well JAKAVI works outside of controlled clinical trials.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ruxolitinib (JAKAVI)
- What this could lead to
- If successful, this study could confirm that ruxolitinib is a safe and effective option for managing graft-versus-host disease in everyday medical practice.
- What could go wrong
- This is an observational study, not a controlled trial, so results may be less definitive. Infections are a known risk with ruxolitinib, and the study focuses on safety monitoring.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 395 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2026
- Expected to finish
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May 2030
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients treated with ruxolitinib for acute and chronic GVHD after its approval.
- Ages
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0 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients with acute and chronic GVHD * Patients treated with ruxolitinib Exclusion Criteria: None Other protocol-defined inclusion/exclusion criteria may apply.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Novartis
RECRUITINGTokyo, 105-6333, Japan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Stem cell infusions put to the test against a tough transplant complication
- Can adding rituximab improve remission in chronic GVHD?
- Can a new drug stop the Body's attack after stem cell transplants?
- Can a new pill tame the immune System's attack after stem cell transplants?
- Could a simple timing change make stem cell transplants safer?
- Can a new pill outperform standard care for a tough transplant complication?