Medication Reaction Clinical Trial
Official title:
Prevention of Epidermal Growth Factor Receptor Inhibitor-Associated Dermatologic Toxicities by Pre-treatment With Topical Tretinoin
Verified date | April 2014 |
Source | Johns Hopkins University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Johns Hopkins Medicine IRB |
Study type | Interventional |
This research is being done to study whether using of topical tretinoin can help prevent the
common rash that patients often get while taking epidermal growth factor inhibitor (EGFR-I)
medications such ascetuximab or erlotinib.
Patients taking EGFR-I medications often develop skin irritation and acne-like bumps on
their face, chest, and other areas. This rash from EGFR-I's is often treated with
moisturizers and topical or oral antibiotics. However, there has not yet been a study
looking at a way to prevent this common side effect from occurring, and topical tretinoin
may be useful in reducing the rash.
Tretinoin 0.025% cream is approved by the Food and Drug Administration (FDA) for the
treatment of acne, acne scarring, and photodamage. It is not approved for use in preventing
rashes associated with EGFR-I's.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | March 2014 |
Est. primary completion date | March 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Age 18 years or over - Scheduled to begin treatment with an EGFR inhibitor drug Exclusion Criteria: - Pregnant or nursing - History of bleeding disorder - History of keloids or large, thick, puffy-looking scars in the last 10 years - Used topical retinoids in the last year (e.g. tretinoin/Retin-A, adapalene/Differin, tazarotene/Tazorac) |
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Johns Hopkins University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | EGFRi rash severity | 8 weeks | No |
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