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Actively Recruiting

Phase 2
Age: 9Years +
All Genders
ID05291845

Candida Antigen and Bivalent HPV Vaccine in the Treatment of Multiple Warts Monotherapy Versus Combined Therapy

Led by Zagazig University · Updated on 2025-06-12

162

Participants Needed

1

Research Sites

9 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the safety and effectiveness of Candida antigen and bivalent HPV vaccine in treating common warts. The trial compares these treatments given alone or combined to see how well they clear warts and prevent recurrence. This is a Phase 2 randomized study involving patients with multiple warts. Participants are divided into three groups one receives Candida antigen injections directly into the largest wart, another receives bivalent HPV vaccine injections, and the third group receives both treatments together. Injections are given every two weeks for up to five sessions or until the warts clear. During the study, patients will be monitored for complete, partial, or no response to treatment over three months. Researchers will also follow up for six months after recovery to check for wart recurrence. Assessments include clinical evaluation of warts and treatment safety throughout the trial.

CONDITIONS

Brief Title

Candida Antigen and Bivalent HPV Vaccine in the Treatment of Multiple Warts

Who Can Participate

Age: 9Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with multiple, recalcitrant, or non-recalcitrant common warts of different sites, sizes, and duration, with or without distant lesions
Not Eligible

You will not qualify if you...

  • Pregnant female
  • Hypersensitivity to Candida antigen or bivalent HPV vaccine

Research Team

R

Reham Essam, MD

R

Reham Essam, MD

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