Ruxolitinib Cream for Acute Skin GVHD

MT
Overseen ByMonica Trapp, BSN, RN, TCTCN
Age: < 65
Sex: Any
Trial Phase: Phase 1
Sponsor: Children's Hospital Medical Center, Cincinnati
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a cream called ruxolitinib to determine its safety for treating acute graft versus host disease (GVHD), a skin condition that can occur after a stem cell transplant, causing redness and itching. The cream is applied directly to the skin twice a day. Suitable participants have undergone a stem cell transplant, are experiencing acute skin GVHD, and are not using other immune-suppressing medications. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, offering participants a chance to be among the first to receive this new treatment.

Is there any evidence suggesting that ruxolitinib cream is likely to be safe for humans?

Studies have shown that ruxolitinib cream is generally safe for people with skin conditions like graft-versus-host disease (GVHD). In previous research, ruxolitinib cream was compared to a placebo (a substance with no active ingredients), and participants using the cream experienced fewer skin rashes and sores. Importantly, those studies reported no serious side effects, confirming its safety.

Ruxolitinib blocks certain proteins called Janus Kinase (JAK) 1/2, which are involved in inflammation, thereby reducing skin problems. Other studies have found the cream to be well-tolerated, with only mild and manageable side effects.

Overall, the evidence suggests that ruxolitinib cream is a promising option for treating skin issues related to GVHD without causing significant harm.12345

Why do researchers think this study treatment might be promising?

Unlike the standard treatments for acute skin graft-versus-host disease (GVHD), which typically involve systemic immunosuppressants and steroids, Ruxolitinib cream offers a targeted, topical approach. This treatment is unique because it contains Ruxolitinib, a JAK inhibitor, which works by blocking specific proteins involved in the inflammatory process. Applying the cream directly to the skin allows it to act precisely where needed, potentially reducing the side effects commonly associated with systemic therapies. Researchers are excited about this approach as it may provide relief from symptoms like erythroderma and pruritus more quickly and with fewer systemic complications.

What evidence suggests that ruxolitinib cream might be an effective treatment for acute skin GVHD?

Research has shown that ruxolitinib cream can help treat skin problems caused by graft-versus-host disease (GVHD). In earlier studies, patients using this cream experienced noticeable improvements in skin rashes and sores. One study found that after 28 days, the cream reduced the affected skin area by 57%, while a placebo cream only reduced it by 28%. Another study demonstrated that the cream worked well for both soft and slightly hardened skin issues. Overall, these results suggest that ruxolitinib cream, which participants in this trial will apply topically, may help ease skin problems in people with GVHD.12456

Who Is on the Research Team?

ZH

Zahra Hudda, MD

Principal Investigator

Children's Hospital Medical Center, Cincinnati

Are You a Good Fit for This Trial?

This trial is for people who have developed acute skin graft versus host disease (GVHD) after receiving a stem cell transplant from a donor. Participants must meet certain health requirements and cannot join if they have conditions that would interfere with the study.

Inclusion Criteria

I have been diagnosed with cancer.
I am between 2 and 35 years old.
I am not currently taking immune-suppressing drugs to treat acute GVHD.
See 2 more

Exclusion Criteria

I have had allergic reactions to topical ruxolitinib.
I do not have any active, uncontrolled skin infections.
I have not taken steroids or experimental treatments in the past 30 days.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Treatment

Participants receive topical ruxolitinib for acute skin GVHD for up to 28 days

4 weeks
Regular monitoring visits

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Ruxolitinib

Trial Overview

The study is testing ruxolitinib cream (1.5%) applied to the skin to see if it is safe and effective in treating acute skin GVHD after donor stem cell transplants.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: RuxolitinibExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Children's Hospital Medical Center, Cincinnati

Lead Sponsor

Trials
844
Recruited
6,566,000+

Citations

722.Allogeneic Transplantation: Acute and Chronic GVHD, ...

Conclusions. Topical ruxolitinib 1.5% cream was effective in treating cutaneous nonsclerotic and superficially sclerotic GvHD as determined by PGA and CAILS.

Paper: Topical Ruxolitinib for Chronic Cutaneous GvHD

Conclusions: This is the first study to characterize the effect of topical JAK1/2 blockade on cutaneous cGVHD. Ruxolitinib 1.5% cream was safe ...

Ruxolitinib Cream Appears Effective Vs Placebo in ...

On days 14 and 28, body surface area was significantly improved with ruxolitinib vs placebo. At day 14, the ruxolitinib side was down by 46% vs ...

Ruxolitinib cream 'effective' in reducing rashes, lesions ...

Topical ruxolitinib cream significantly reduced skin manifestations caused by cutaneous graft-versus-host disease compared with vehicle cream, ...

Topical Ruxolitinib for Cutaneous Chronic Graft Versus ...

Most cGVHD therapies have serious side effects. The cream ruxolitinib inhibits proteins that may play a role in cGVHD. Objective: To test the safety and ...

What data is available to support the off-label use of ...

Ruxolitinib 1.5% cream was safe and effective compared to placebo in treating cutaneous nonsclerotic and superficially sclerotic GvHD. Responders to ruxolitinib ...