25 Participants Needed

Belumosudil + Rituximab for Graft-versus-Host Disease

CG
Scott Solomon, MD profile photo
Overseen ByScott Solomon, MD
Age: 18+
Sex: Any
Trial Phase: Phase 2
Sponsor: Northside Hospital, Inc.
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial
Breakthrough TherapyThis drug has been fast-tracked for approval by the FDA given its high promise

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a combination of two treatments, belumosudil (a new potential drug) and rituximab, to evaluate their effectiveness for people with chronic graft-versus-host disease (cGVHD). cGVHD can occur after a stem cell or bone marrow transplant when donor cells attack the recipient's body. The trial aims to assess the safety and effectiveness of these treatments. Suitable candidates for this trial are those experiencing their first episode of cGVHD requiring immunosuppressants and who have not yet undergone extensive treatment. As a Phase 2 trial, this research focuses on measuring the treatment's effectiveness in an initial, smaller group of people.

Will I have to stop taking my current medications?

The trial does not specify if you need to stop taking your current medications. However, it mentions that participants should not have received more than 10 days of corticosteroids or other systemic immunosuppressive agents for cGVHD before joining the study.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research shows that belumosudil is generally safe for people with chronic graft-versus-host disease (cGVHD). Earlier studies found it safe over a long period, with most people not experiencing serious side effects. The FDA has approved belumosudil for treating cGVHD that has returned or not responded to other treatments, confirming its safety record for this condition.

Rituximab has been used for many years to treat various conditions, including some autoimmune diseases and certain cancers. This extensive history provides substantial information about its safety. Most people tolerate rituximab well, although it can cause side effects in some individuals.

Together, belumosudil and rituximab have shown promising safety results in past research and approvals. While researchers continue to study the combination, these findings help reassure about their potential safety in humans.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about Belumosudil plus Rituximab for graft-versus-host disease because this combination offers a novel approach compared to standard treatments like corticosteroids and immunosuppressants. Belumosudil works uniquely by targeting the ROCK2 pathway, which plays a key role in immune system regulation, potentially reducing inflammation more effectively. Rituximab, known for targeting CD20 on B cells, complements this by reducing the immune response that contributes to the disease. Together, they promise a more targeted attack on the disease, which could lead to better outcomes for patients.

What evidence suggests that Belumosudil and Rituximab could be effective for graft-versus-host disease?

Research has shown that belumosudil can help treat chronic graft-versus-host disease (cGVHD). One study found that 65% of patients responded well to belumosudil, with many experiencing improvement. Patients reported a better quality of life and required fewer steroids, which are often used to manage symptoms. Belumosudil was generally well-tolerated, with benefits lasting over time. Although less direct evidence exists for using rituximab with belumosudil, rituximab targets specific immune cells and might complement belumosudil. In this trial, participants will receive a combination of these treatments, which shows promise for helping people with cGVHD.14678

Who Is on the Research Team?

Scott Solomon MD — The Blood and ...

Scott Solomon, MD

Principal Investigator

BMTGA/Northside Hospital

Are You a Good Fit for This Trial?

This trial is for individuals with a new diagnosis of chronic Graft-Versus-Host Disease (cGVHD) who haven't been treated yet, or have had less than 10 days of corticosteroids. Participants must be in good physical condition (KPS >/= 70%) and have adequate blood cell counts without recent transfusions. People with HIV, active hepatitis B or C, severe liver issues, poor kidney function, uncontrolled infections or heart problems cannot join.

Inclusion Criteria

My blood counts are within the required range without transfusions for a week.
I have started treatment for cGVHD less than 10 days ago.
I am mostly able to care for myself and carry out daily activities.
See 1 more

Exclusion Criteria

I do not have an active hepatitis B or C infection.
My kidney function is low, with a filtration rate under 30 mL/min.
I have ongoing or returning graft-versus-host disease.
See 5 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive Belumosudil and Rituximab as primary treatment for chronic graft-versus-host disease

12 weeks

Follow-up

Participants are monitored for safety and effectiveness after treatment

12 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Belumosudil
  • Rituximab
Trial Overview The study is testing the combination of two drugs—Belumosudil and Rituximab—as a primary treatment for cGVHD. It's an open-label Phase 2 trial which means everyone knows what treatment they're getting and it's fairly early in the testing process to see if it works well and is safe.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: Belumosudil Plus RituximabExperimental Treatment2 Interventions

Belumosudil is already approved in United States, Canada for the following indications:

🇺🇸
Approved in United States as Rezurock for:
🇨🇦
Approved in Canada as Rholistiq for:

Find a Clinic Near You

Who Is Running the Clinical Trial?

Northside Hospital, Inc.

Lead Sponsor

Trials
26
Recruited
1,100+

Sanofi

Industry Sponsor

Trials
2,246
Recruited
4,085,000+
Paul Hudson profile image

Paul Hudson

Sanofi

Chief Executive Officer since 2019

Degree in Economics from Manchester Metropolitan University

Christopher Corsico profile image

Christopher Corsico

Sanofi

Chief Medical Officer

MD from Cornell University, MPH in Chronic Disease Epidemiology from Yale University

Published Research Related to This Trial

Belumosudil, an oral medication targeting ROCK2, showed a high overall response rate of 74% for the 200 mg daily dose and 77% for the 200 mg twice daily dose in patients with chronic graft-versus-host disease (cGVHD) after multiple prior treatments, indicating its efficacy in this challenging condition.
The treatment was well tolerated, with a median duration of response of 54 weeks and significant symptom reduction in 59% to 62% of subjects, while adverse events were consistent with those expected in cGVHD patients, suggesting a favorable safety profile.
Belumosudil for chronic graft-versus-host disease after 2 or more prior lines of therapy: the ROCKstar Study.Cutler, C., Lee, SJ., Arai, S., et al.[2022]
Rituximab, an anti-B cell therapy, shows promise in reducing the incidence and severity of acute graft-versus-host disease (GVHD) in patients undergoing allogeneic hematopoietic cell transplantation, although most evidence comes from non-randomized studies using higher doses.
Rituximab is also effective in treating corticosteroid-refractory chronic GVHD, particularly for skin and mucosal symptoms, and preliminary studies suggest it may lower the rate of chronic GVHD when administered post-transplant.
Rituximab for prevention and treatment of graft-versus-host disease.Kharfan-Dabaja, MA., Cutler, CS.[2021]
In a retrospective analysis of 3,803 adult patients with B-cell malignancies undergoing allogeneic hematopoietic cell transplantation, the addition of rituximab to reduced intensity conditioning regimens did not significantly improve major transplant outcomes such as overall survival, disease-free survival, or non-relapse mortality.
The study found similar rates of acute graft-versus-host disease (GVHD) between patients receiving rituximab and those who did not, indicating that rituximab may not provide additional benefits in preventing GVHD in this context.
Addition of Rituximab in Reduced Intensity Conditioning Regimens for B-Cell Malignancies Does Not Influence Transplant Outcomes: EBMT Registry Analyses Following Allogeneic Stem Cell Transplantation for B-Cell Malignancies.Tomaszewska, A., Jagasia, M., Beohou, E., et al.[2021]

Citations

Belumosudil and Rituximab for Primary Treatment of Chronic ...This is an open-label, Phase 2 study designed to evaluate the safety and efficacy of belumosudil and rituximab as primary treatment of cGVHD.
Belumosudil for treating chronic graft-versus-host disease ...Clinical trial evidence suggests that taking belumosudil improves people's symptoms, but it was not compared directly with best available ...
Belumosudil for chronic graft-versus-host disease after 2 or ...In that study, belumosudil demonstrated a pooled ORR of 65%, improvements in QOL (as measured by the LSS) and reductions in CS use in subjects ...
NCT03640481 | Efficacy and Safety of KD025 in Subjects ...This is a Phase 2, randomized, multicenter study to evaluate the efficacy and safety of KD025 in subjects with Chronic Graft Versus Host Disease (cGVHD)
Analysis of Long-Term Results from the KD025-208 and ...Durability of response was shown through an increase in DOR, FFS, and TTNT. •. Belumosudil was well tolerated in patients with cGVHD after long-term follow-up.
Safety and efficacy of the ROCK-2-inhibitor Belumosudil in ...In this retrospective real-world analysis, we report safety and efficacy data of belumosudil treatment from 5 German/Swiss transplant centers.
NCT03640481 | Efficacy and Safety of KD025 in Subjects ...Correlation of Patient-Reported Outcomes with Clinical Organ Responses: Data from the Belumosudil Chronic Graft-versus-Host Disease Studies. Transplant Cell ...
Efficacy and Safety of Belumosudil as Compared with Best ...Belumosudil was FDA-approved in the United States (US) for the treatment of relapsed/refractory chronic graft-versus-host disease (cGVHD) based ...
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Terms of Service·Privacy Policy·Cookies·Security