8 Participants Needed

IV IgG for Dystrophic Epidermolysis Bullosa

(IV IgG Trial)

CR
Overseen ByClinical Research Coordinator
Age: Any Age
Sex: Any
Trial Phase: Phase 1 & 2
Sponsor: M. Peter Marinkovich
Must be taking: Vyjuvek
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 treatment called IV IgG (intravenous immunoglobulin) to determine if it aids in healing skin wounds in individuals with Recessive Dystrophic Epidermolysis Bullosa (RDEB) when combined with another treatment, VYJUVEK. The goal is to discover if this combination results in fewer and faster-healing wounds and to assess its impact on certain blood proteins. Potential candidates for this study include those with RDEB who are receiving ongoing VYJUVEK treatment and experience skin blistering over more than 5% of their body. As a Phase 1, Phase 2 trial, this research aims to understand how the treatment works and measure its effectiveness in an initial group of participants.

Will I have to stop taking my current medications?

The trial protocol does not specify whether you need to stop taking your current medications. However, ongoing VYJUVEK treatment is required for participation.

Is there any evidence suggesting that IV IgG treatment is likely to be safe for humans?

Research has shown that IV IgG treatment holds promise for skin conditions similar to dystrophic epidermolysis bullosa (DEB). In past studies, IV IgG significantly helped, with 78.6% of patients experiencing disease remission in a similar condition called epidermolysis bullosa acquisita. This suggests that IV IgG might be well-tolerated.

Additionally, IV IgG is already used safely for other conditions. For instance, it serves as a safe and effective treatment for juvenile dermatomyositis, a muscle disease. Patients treated with IV IgG had good results and did not experience relapses over long periods.

While limited data exists on IV IgG specifically for DEB, these previous findings suggest it has a good safety profile. Participants in this trial can expect potential benefits with a reasonable chance of tolerability.12345

Why do researchers think this study treatment might be promising?

Unlike the standard treatments for dystrophic epidermolysis bullosa, which often focus on topical applications and wound care, IV IgG offers a novel approach by utilizing immune globulin delivered intravenously. This treatment is unique because it potentially strengthens the body's immune response, helping to manage the condition from within, rather than just treating the symptoms externally. Researchers are excited because this could mean more comprehensive control of the disease and potentially fewer complications for patients.

What evidence suggests that IV IgG might be an effective treatment for Recessive Dystrophic Epidermolysis Bullosa?

Research has shown that IV IgG therapy might help treat conditions like dystrophic epidermolysis bullosa (EB). In some studies, IV IgG reduced inflammation, a major issue in EB. For people with EB, who often have non-healing wounds, IV IgG might help by adjusting the body's immune response. Although results have varied, some patients experienced wound healing improvements between 30% and 80%. In this trial, participants will continue their prescribed Vyjuvek application and receive IV IgG treatment. These findings suggest that IV IgG could be a useful addition to current treatments for improving wound healing.16789

Who Is on the Research Team?

MP

Matt P Marinkovich, MD

Principal Investigator

Associate Professor of Dermatology

Are You a Good Fit for This Trial?

This trial is for individuals with Recessive Dystrophic Epidermolysis Bullosa (RDEB), a rare skin condition. Participants should have active wounds that could potentially heal better with treatment. Specific eligibility criteria are not provided, but typically include age, health status, and disease severity.

Inclusion Criteria

I have skin blistering covering more than 5% of my body.
I have a wound larger than 20 cm^2 that can be treated weekly.
My tests show high levels of C7 antibodies, indicating EBA.
See 3 more

Exclusion Criteria

I have had blood clots in the past.
I have IgA deficiency.
I have a history of heart failure.
See 1 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Observational

Participants undergo a 3-month observational period, continuing their prescribed Vyjuvek application

12 weeks

Treatment

Participants continue Vyjuvek application and receive IV IgG treatment

9 months

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • IV IgG
Trial Overview The trial tests if IV IgG can improve wound healing in RDEB patients when used alongside VYJUVEK therapy. It also examines the effect on C7 and HSV-1 antibody levels in the blood which may indicate improved skin health.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: Intra-Personal ControlExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

M. Peter Marinkovich

Lead Sponsor

Trials
1
Recruited
8+

Epidermolysis Bullosa Research Partnership

Collaborator

Trials
5
Recruited
90+

Citations

Targeting Collagen VII Antibodies With IV IgG in Dystrophic ...The study objective is to see if IV IgG treatment in Recessive Dystrophic Epidermolysis Bullosa (RDEB) skin in conjunction with VYJUVEK treatment improves wound ...
2.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/32506551/
Promising Effect of Intravenous Immunoglobulin Therapy ...In severe cases, unresponsive to other therapies, IVIG may be a preferable therapeutic approach to modulate the inflammatory response in patients with EBP.
Promising effect of intravenous immunoglobulin therapy for ...Promising effect of intravenous immunoglobulin therapy for epidermolysis bullosa pruriginosa. Pelin Ertop MD,.
Tissue and systemic inflammation in dystrophic epidermolysis ...For outcomes with multiple available studies, we performed an exploratory network meta-analysis to compare the standardized mean difference in ...
Treatment of Epidermolysis Bullosa and Future DirectionsResults have shown variable outcomes, with wound healing improvement ranging from 30 to 80%. However, the efficacy has not consistently ...
6.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/37150538/
Special focus on indication and combination therapyIn epidermolysis bullosa acquisita, treatment with IVIg led to 78.6% disease remission; no data were available regarding the treatment with RTX + IVIg in this ...
IV IgG for Dystrophic Epidermolysis BullosaThe IV IgG medical study, being run by M. Peter Marinkovich, is evaluating whether IV IgG will have tolerable side effects & efficacy for patients with ...
Dermatology and Immunoglobulin Therapy: Who to Treat ...In the treatment of juvenile dermatomyositis, IVIG therapy occupies a position as an effective and safe alternative, particularly when administered ...
Clinical outcome and post-treatment long-term follow-upIn all 10 patients, a satisfactory clinical response was observed, and during followup (29-123 months), no relapse was observed [220] .
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