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Can adding rituximab improve remission in chronic GVHD?

NCT ID NCT01135641

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Sep 14, 2026 · Last updated Sep 15, 2026 · Updated 1 time

Summary

This Phase II trial tests whether adding rituximab to standard first-line treatment with ciclosporine and corticosteroids improves remission rates in adults who develop chronic graft versus host disease after a stem cell transplant. Participants receive rituximab infusions once a week for four weeks alongside their usual immunosuppressive therapy. Researchers measure how many participants reach complete or partial remission at 12 months and track side effects, treatment failure, and steroid use.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
rituximab added to standard immunosuppressive treatment with ciclosporine and corticosteroids
What this could lead to
If it works, adding rituximab could help more people with chronic graft versus host disease reach remission and reduce their need for long-term steroids.
What could go wrong
This is a small Phase II trial with 25 participants, so any benefit may not hold up in larger studies. Rituximab and stronger immunosuppression can raise the risk of infections and other complications.

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.

Phase

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

25 people

The number who actually took part.

Start date

Jun 2010

Finished

Mar 2014

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Adult patients (≥18 years) who have received a first allogeneic stem cell transplantation for a hematological disease * Confirmed diagnosis of first episode of chronic GVHD requiring systemic immunosuppressive therapy. Chronic GVHD diagnosis is defined according to the NIH Working Group Consensus. Chronic GVHD diagnosis will be based on the evaluation of the severity of the different clinical manifestations including : 1. Ocular, oral and mucosal symptoms, 2. Performance status evaluation, 3. Pulmonary function evaluation, 4. Cutaneous evaluation measured by the percentage of extension of manifestations of liche-noid or sclerodermatous aspects, eventually confirmed with a biopsy whenever possible, 5. Evaluation of the musculoskeletal manifestations, especially the amplitude of the rele-vant articulations, 6. Evaluation of liver involvement (Total bilirubin, Transaminases, Phosphatase alcalines and Gamma GT). * Any source of hematopoietic stem cells is authorized. * Any category of conditioning regimen prior to allo-SCT is authorized. * Any type of stem cell donors is authorized. * Signed informed consent. * Any prior GVHD prophylaxis previously used is accepted. * Absence of contra-indications to the use of Rituximab. * Subjects affiliated with an appropriate social security system. * Women who are of childbearing potential must have a negative serum pregnancy test and agree to use a medically acceptable method of contraception throughout the study and for 3 months following the end of the study. Exclusion Criteria: * Patient developing acute GVHD (whether early or "late onset" form) * A "limited" form of chronic GVHD not requiring systemic immunosuppressive therapy * Treatment with prednisone (or equivalent) at doses higher than 1 mg/kg/day at the time of enrollment. * GVHD occurring following donor lymphocytes infusion (DLI) * Not the first episode of chronic GVHD needing systemic immunosuppressive therapy * Neutropenia \<500/µL * Second allogeneic stem cell transplant * Uncontrolled systemic infection which in the opinion of the investigator is associated with an increased risk of the patient's death within 1 month after the start of therapy * Severe neurological or psychiatric disorders * Denied informed consent * Pregnancy

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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.

Contacts and locations

Locations

  • Nantes University Hospital

    Nantes, 44093, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.