Skip to main content

Cervical Intraepithelial Neoplasia 3

1
Pipeline Programs
1
Companies
4
Clinical Trials
0
Approved Products

Pipeline by Development Stage

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

Competitive Landscape

1 companies ranked by most advanced pipeline stage

Genexine
GenexineKorea - Seoul
4 programs
1
GX-188E administered by electroporationPhase 11 trial
GX-188EN/A1 trial
GX-188EN/A1 trial
GX-188E, GX-I7N/A1 trial
Active Trials
NCT02100085Unknown9Est. Jan 2018
NCT02411019Unknown67Est. Nov 2018
NCT03206138Unknown50Est. Oct 2018
+1 more trials

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
GenexineGX-188E administered by electroporation
GenexineGX-188E, GX-I7
GenexineGX-188E
GenexineGX-188E

Clinical Trials (4)

Total enrollment: 135 patients across 4 trials

NCT01634503GenexineGX-188E administered by electroporation

Safety of GX-188E DNA Therapeutic Vaccine Administered by Electroporation to Cervical Intraepithelial Neoplasia Grade 3

Start: Nov 2012Est. completion: Feb 20149 patients
Phase 1Completed
NCT03206138GenexineGX-188E, GX-I7

Safety and Efficacy of GX-188E Administered Via EP Plus GX-I7 or Imiquimod.

Start: May 2017Est. completion: Oct 201850 patients
N/AUnknown

Safety and Efficacy of GX-188E DNA Therapeutic Vaccine Administered by Electroporation After Observation

Start: Mar 2015Est. completion: Nov 201867 patients
N/AUnknown

Safety and Efficacy of GX-188E DNA Therapeutic Vaccine Administered by Electroporation After Observation

Start: Feb 2014Est. completion: Jan 20189 patients
N/AUnknown

Phase Legend

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

Key Insights

1 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.