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Study identifier: NCT03207906 Synced from ClinicalTrials.gov · July 28, 2026
● Completed

A Trial to Evaluate the Efficacy and Safety of Two Concentrations of VBP-926 Solution for the Treatment of Chemotherapy-associated Paronychia in Cancer Patients

Condition: Chemotherapy-Associated Paronychia  ·  Sponsor: Veloce BioPharma LLC

PhasePhase 2
Planned participants102
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Paronychia is inflammation of the skin surrounding the nail that leads to secondary infection. Iatrogenic paronychia has been clearly associated with cancer chemotherapies. This phase-2 trial is a dose finding study and will evaluate topical VBP-926 solution against a vehicle control.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (8)

Compassionate Cancer CareFountain Valley, California, United States
Northwestern University Department of DermatologyChicago, Illinois, United States
Washington UniversitySt Louis, Missouri, United States
Memorial Sloan Kettering Cancer CenterNew York, New York, United States
Montefiore Einstein Center for Cancer CareThe Bronx, New York, United States
Oncology Specialists of CharlotteCharlotte, North Carolina, United States
Ohio State UniversityColumbus, Ohio, United States
Bryn Mawr Skin & Cancer InstituteBryn Mawr, Pennsylvania, United States

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Source record: clinicaltrials.gov/study/NCT03207906