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Spots Global Cancer Trial Database for FLASH [Fluorescent Light Activated Synthetic Hypericin] Clinical Study: Topical SGX301 (Synthetic Hypericin) for the Treatment of Cutaneous T-Cell Lymphoma (Mycosis Fungoides)

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Trial Identification

Brief Title: FLASH [Fluorescent Light Activated Synthetic Hypericin] Clinical Study: Topical SGX301 (Synthetic Hypericin) for the Treatment of Cutaneous T-Cell Lymphoma (Mycosis Fungoides)

Official Title: A Phase 3 Multicenter, Randomized, Double-Blind, Placebo Controlled Study to Determine the Efficacy of Topical SGX301 (Synthetic Hypericin) and Fluorescent Bulb-Light Irradiation for the Treatment of Cutaneous T-Cell Lymphoma

Study ID: NCT02448381

Study Description

Brief Summary: To evaluate the use of SGX301, a topical photosensitizing agent, to treat patients with patch/plaque phase cutaneous T-cell lymphoma (mycosis fungoides).

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Alabama Birmingham, Birmingham, Alabama, United States

University of Arizona, Phoenix, Arizona, United States

Mayo Clinic, Scottsdale, Arizona, United States

University of Arkansas, Little Rock, Arkansas, United States

Stanford University, Palo Alto, California, United States

Therapeutics Clinical Research, San Diego, California, United States

Olympian Clinical Research, Clearwater, Florida, United States

Leon Medical Research, Miami, Florida, United States

Medical Professional Clinical Research, Miami, Florida, United States

University of South Florida, Tampa, Florida, United States

Northwestern University, Chicago, Illinois, United States

Rush University, Chicago, Illinois, United States

Dawes Fretzin Dermatology Group, Indianapolis, Indiana, United States

Tulane University, New Orleans, Louisiana, United States

University of Maryland, Baltimore, Maryland, United States

University of Minnesota, Minneapolis, Minnesota, United States

Washington University, Saint Louis, Missouri, United States

Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, United States

Rochester Skin Lymphoma Medical Group, Fairport, New York, United States

Columbia University Medical Center, New York, New York, United States

Stony Brook Medicine, Stony Brook, New York, United States

PMG Research of Wilmington, Wilmington, North Carolina, United States

University Hospitals Cleveland Medical Center, Cleveland, Ohio, United States

Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States

Jefferson Dermatology, Philadelphia, Pennsylvania, United States

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States

Medical University of South Carolina, Charleston, South Carolina, United States

Vanderbilt University, Nashville, Tennessee, United States

MD Anderson, Houston, Texas, United States

Austin Institute for Clinical Research, Pflugerville, Texas, United States

INOVA Schar Cancer Institute, Fairfax, Virginia, United States

Virginia Clinical Research, Norfolk, Virginia, United States

Seattle Care Cancer Center, Seattle, Washington, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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