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Topical Cream for Mastocytosis
Phase 2
Waitlist Available
Led By Joseph Butterfield, MD
Research Sponsored by Joseph Butterfield
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new cream or ointment for patients with skin lesions caused by mastocytosis. The treatment is applied directly to the skin to help reduce or heal the lesions. Tacrolimus ointment is the first of a new class of treatments for skin conditions.
Who is the study for?
Adults aged 18-80 with biopsy-proven cutaneous mastocytosis can join this trial. Women must not be pregnant, plan to become pregnant, or breastfeed and should use effective birth control. Participants shouldn't have had UVB skin treatment or used corticosteroids recently.
What is being tested?
The study is testing a new topical cream combining sodium cromolyn, diphenhydramine, and trolamine salicylate for treating skin lesions caused by mastocytosis to see if it's effective and tolerable.
What are the potential side effects?
Potential side effects may include local skin reactions like redness, itching or irritation at the site of application due to the active ingredients in the cream.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Cutaneous Symptom Relief
SkinDex-16 Quality of Life Questionnaire
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Skin GuardExperimental Treatment1 Intervention
Skin cream combination of ingredients includes 2 agents which target mast cell mediators and one agent which globally reduces mast cell degranulation combined in an emollient cream base:
Vanicream: Over the counter emollient cream Diphenhydramine Antihistamine Trolamine salicylate Prostaglandin inhibitor, antiinflammatory Cromolyn Sodium Mast cell degranulation inhibitor
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Mastocytosis treatments primarily target mast cells and the inflammatory pathways they activate. Common treatments include mast cell stabilizers, which prevent the release of histamine and other mediators, and antihistamines, which block the effects of histamine on tissues.
Topical corticosteroids are also used to reduce local inflammation. These mechanisms are crucial for Mastocytosis patients as they help manage symptoms like itching, redness, and swelling by directly addressing the underlying cellular processes.
The novel topical preparation being studied likely aims to enhance these effects by targeting mast cells or specific inflammatory pathways more effectively.
Subcutaneous birch pollen allergen immunotherapy with a depigmented polymerized extract shows only sustained and long-term efficacy in a subgroup of monosensitized adults and adolescents with allergic rhinitis.Comparative efficacy of once-daily therapy with inhaled corticosteroid, leukotriene antagonist or sustained-release theophylline in patients with mild persistent asthma.
Subcutaneous birch pollen allergen immunotherapy with a depigmented polymerized extract shows only sustained and long-term efficacy in a subgroup of monosensitized adults and adolescents with allergic rhinitis.Comparative efficacy of once-daily therapy with inhaled corticosteroid, leukotriene antagonist or sustained-release theophylline in patients with mild persistent asthma.
Find a Location
Who is running the clinical trial?
Joseph ButterfieldLead Sponsor
Joseph Butterfield, MDPrincipal Investigator - Mayo Clinic
Mayo Clinic Hospital-Rochester Saint Marys Campus
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have been exposed to UVB radiation on your skin in the past 6 months.You are between 18 and 80 years old.People who are at higher risk or need extra protection during the study.You have received UV light therapy or have been sunbathing.You have been diagnosed with skin mastocytosis, with or without signs of it spreading to other parts of your body.You have been using skin lightening products like corticosteroids or bleaching creams regularly in the past month.You haven't used any corticosteroid creams or pills for a month before joining the study.
Research Study Groups:
This trial has the following groups:- Group 1: Skin Guard
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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