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Condyloma

0
Pipeline Programs
4
Companies
3
Clinical Trials
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
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0
0
0
0
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Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

4 companies ranked by most advanced pipeline stage

MSD
MSDIreland - Ballydine
1 program
Effectiveness Study of Gardasil on CondylomaN/A1 trial
Active Trials
NCT01553994Completed500,000Est. Dec 2010
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
1 program
Effectiveness Study of Gardasil on CondylomaN/A
CEL-SCI
CEL-SCIVA - Vienna
1 program
Leukocyte Interleukin, Injection 200IUPHASE_11 trial
Active Trials
NCT02115919Terminated4Est. Jan 2016
Vaxart
VaxartSOUTH SAN FRANCISCO, CA
1 program
AP611074 5% gelPHASE_21 trial
Active Trials
NCT02724254Completed218Est. Jul 2018

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
VaxartAP611074 5% gel
CEL-SCILeukocyte Interleukin, Injection 200IU
MSDEffectiveness Study of Gardasil on Condyloma

Clinical Trials (3)

Total enrollment: 500,222 patients across 3 trials

NCT02724254VaxartAP611074 5% gel

A Study to Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of Twice Daily Topical Applications of AP611074 5% Gel for up to 16 Weeks in Condyloma Patients

Start: Jan 2016Est. completion: Jul 2018218 patients
Phase 2Completed
NCT02115919CEL-SCILeukocyte Interleukin, Injection 200IU

Safety Study of Multikine in the Treatment of Perianal Warts

Start: Apr 2014Est. completion: Jan 20164 patients
Phase 1Terminated
NCT01553994MSDEffectiveness Study of Gardasil on Condyloma

Effectiveness Study of Gardasil on Condyloma

Start: Jun 2006Est. completion: Dec 2010500,000 patients
N/ACompleted

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

4 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.