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NCT05156541: ING-HPV-1

Study of the Efficacy and Safety of the Drug Ingaron (Interferon-gamma) in the Treatment of Anogenital Warts

Completed Phase 3 Last updated 14 December 2021
What this trial tests

Phase 3 trial testing Interferon gamma human recombinant (IFN-G) in Human Papillomavirus Infection in 30 participants. Completed in 15 July 2010.

Timeline
18 May 2009
Primary endpoint
30 June 2010
15 July 2010

Quick facts

Lead sponsorSPP Pharmaclon Ltd.
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment30
Start date18 May 2009
Primary completion30 June 2010
Estimated completion15 July 2010
Sites1 location across Russia

Drugs / interventions tested

Conditions studied

Sponsor

SPP Pharmaclon Ltd. — full company profile →

Who can join

Adults 18 to 50, any sex, with Human Papillomavirus Infection or Anogenital Warts. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary purpose of this study is to evaluate the effectiveness of destructive therapy for anogenital warts in combination with the use of Ingaron in comparison with destructive therapy.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Interferon gamma human recombinant (IFN-G)

Trials testing the same drug.

Other recruiting trials for Human Papillomavirus Infection

Currently open trials in the same condition.

Other SPP Pharmaclon Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05156541.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing