StrataCTX® as a Steroid Sparing Device
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Details and patient eligibility
About
The purpose is to determine if StrataCTX® can be used as a steroid sparing agent for the treatment of cutaneous reactions related to, cutaneous T Cell lymphoma (CTCL) and chemotherapy/immunotherapy treatments than the current standard treatment - topical steroids - in people who are receiving treatment for CTCL, or chemotherapy/immunotherapy for solid/hematologic malignancies. Subjects will have CTCL and are being treated with topical steroids, or being treated with chemotherapy/immunotherapy for another condition and have had cutaneous reactions that have warranted initiation of topical steroids.
Full description
Topical steroids are the mainstays of treatment for many cutaneous reactions and disorders. Steroids are known to cause many side effects and few effective pharmacologic alternatives exist. Contact dermatitis is observed in 56% of patients with cutaneous T-cell lymphoma (CTCL) being treated with topical mechlorethamine gel. This usually requires chronic treatment with mid-to high-potency steroids. Numerous chemo/immunotherapies are associated with cutaneous reactions including paronychia, hand and foot syndrome, and acneiform rash. Skin toxicity often requires dose reduction of cancer therapies and a variety of skin directed therapies including topical antibiotics and topical steroids. Cutaneous reactions are often the earliest manifestation of acute graft versus host disease. Skin manifestations can be debilitating and treatment usually requires high potency topical steroids. Additional therapies are needed for the treatment of disorders that rely on topical steroids.
Enrollment
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Ages
Volunteers
Inclusion criteria
- Age ≥ 18 years
- Ability to sign informed consent document
- Patient with a diagnosis of CTCL who have contact dermatitis to topical mechlorethamine gel
- Patients with a diagnosis of CTCL who have intractable pruritis
- Patients with a diagnosis of CTCL who rely heavily on topical steroids for symptomatic relief
- Patients on chemo/immunotherapy with drug induced rash
Exclusion criteria
- Patients currently undergoing radiotherapy
- Patients currently receiving oral steroids
- Patients who are unable to apply topical medications
Trial design
Primary purpose
Allocation
Interventional model
Masking
70 participants in 1 patient group
Trial contacts and locations
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Central trial contact
Larisa Geskin, MD
Data sourced from clinicaltrials.gov
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