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Clinical Trial Summary

To evaluate drug safety and efficacy in patients treated with Nowarta110 and to determine therapeutic activity against Plantar Warts

- Clinical Tolerance

- Clinical Recovery

- Evaluate Safety


Clinical Trial Description

Plantar Warts occur on the soles (plantar surface of feet) and can be severely debilitating for patients even for normal walking. The severity and magnitude of the warts can vary, but they are the cause of much pain and discomfort for all age groups. Nowarta 110 has been evaluated for the therapy of plantar warts caused by the HPV virus, (HPV infection). Clinical experience in a totals of 124 patients receiving Nowarta 110 for 5 weeks treatment in multiple clinics overseas has demonstrated the potential of Nowarta110 with absolutely no side effect. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02338336
Study type Interventional
Source Nowarta Biopharma Inc
Contact
Status Completed
Phase Phase 1/Phase 2
Start date February 2015
Completion date December 2015

See also
  Status Clinical Trial Phase
Recruiting NCT01330615 - Efficacy Trial of Eutectic Lidocaine/Prilocaine Cream 5% (EMLA) for Analgesia Prior to Cryotherapy of Verrucae Plantaris N/A
Terminated NCT01059110 - Comparison of Five Treatments in Patients With Plantar Warts Phase 4
Active, not recruiting NCT02640820 - Evaluate the Effectiveness and Safety of DPCP Ointment (Samcyprone™) on the Clearance of Verruca Vulgaris (Common Warts) Phase 2
Terminated NCT02861404 - Evaluation of Viral Status of Patients With Plantar Warts Included in VRAIE Study, Non-responder to Study Treatment N/A