Clinical Trials Directory

Trials / Terminated

TerminatedNCT00117884

Efficacy of 851B Gel for Treating High-Risk Cervical Human Papillomavirus Infection in Women.

A Randomized, Double-blind, Placebo-Controlled, Dose Response Study to Evaluate 851B Gel Delivered Intravaginally Twice a Week for Two, Three-Week Cycles in Women Who Are Positive For High-Risk Genotypes of Human Papillomavirus and Have Mild Cytological Abnormalities

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
240 (actual)
Sponsor
Takeda · Industry
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to evaluate efficacy of 851B gel over a range of concentrations and dosing regimens on high-risk cervical human papillomavirus infection in women.

Detailed description

Cervical cancer is caused by infection with specific genotypes of the human papillomavirus referred to as oncogenic or high-risk human papillomavirus. Current epidemiologic evidence suggests that 80% of sexually active women will become infected during their lifetime with human papillomavirus and 50% of these infections will be due to high-risk human papillomavirus. With US annual rates of cervical cancer now in the range of 13,000/year, a very substantial number of women are left with uncertainty regarding whether their infection will clear spontaneously or progress to cancer. Subjects participating in this study were required to visit the clinic for approximately 15 or 16 visits, and maintain a diary of self-dosing and menstruation cycles. The total time of participation in this study was approximately 27 months.

Conditions

Interventions

TypeNameDescription
DRUG851B851B 0.15% formulation, gel, topically, twice a week for 2 cycles.
DRUG851B851B 0.15% formulation, gel, topically, twice a week for 2 cycles.
DRUG851B851B 0.15% formulation, gel, topically, twice a week for 2 cycles.
DRUG851B851B 0.15% formulation, gel, topically, twice a week for 2 cycles.
DRUG851B851B 0.15% formulation, gel, topically, twice a week for 2 cycles.
DRUG851B851B 0.15% formulation, gel, topically, twice a week for 2 cycles.
DRUG851B851B 0.15% formulation, gel, topically, twice a week for 2 cycles.
DRUG851B851B 0.15% formulation, gel, topically, twice a week for 2 cycles.
DRUG851B851B 0.15% formulation, gel, topically, twice a week for 2 cycles.
DRUG851B851B 0.15% formulation, gel, topically, twice a week for 2 cycles.
DRUG851B851B 0.15% formulation, gel, topically, twice a week for 2 cycles.

Timeline

Start date
2006-04-01
Primary completion
2008-06-01
Completion
2008-06-01
First posted
2005-07-11
Last updated
2016-08-19

Locations

23 sites across 2 countries: United States, Canada

Source: ClinicalTrials.gov record NCT00117884. Inclusion in this directory is not an endorsement.