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Therapeutic Areas: Dermatology | Oncology
Disease Category: Mycosis Fungoides
Location: United States, FL

Clinical Trial Details


Research Study Summary

A Prospective, Observational, US-based Study Assessing Outcomes, Adverse Events, Treatment Patterns, and Quality of Life in Patients Diagnosed With Mycosis Fungoides Cutaneous T-cell Lymphoma and Treated With Valchlor®


The Valchlor PROVe study is a multi-center, prospective, observational, US-based drug study that longitudinally follows patients with MF-CTCL who are receiving therapy with Valchlor. Patients will be followed prospectively for a maximum of 1 year from the date of signed informed consent (enrollment) until end of study. Continuation in the study is not contingent on continuation of Valchlor.

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CW ID: 212054
Date Last Changed: March 8, 2016

Clinical Trial Snapshot

Both Male and Female
18 and up
Overall Status
Lead Sponsor
1 Years
Facility Type


Inclusion Criteria:

  • All adult patients (≥ 18 years of age) diagnosed with MF CTCL and being treated with Valchlor. This includes patients newly initiating Valchlor OR patients continuing treatment with Valchlor:
    • Patients newly initiating Valchlor are patients who have their first office visit after having initiated Valchlor
    • Patients continuing treatment with Valchlor includes patients who are actively taking Valchlor on the day of enrollment
  • Signed patient informed consent

Exclusion Criteria:

  • None

More Info

Protocol #: AC-079A501


Diana Amick
University of South Florida- Morsani Center for Advanced Healthcare
13330 USF Laurel Drive
Tampa, FL 33613
Phone: 813-396-9179

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