CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 80 enrolled
Drug / intervention
HerpV and QS-21 +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01687595
NCT01687595Phase 2Completed

A Phase 2a, Multicenter, Double-blinded, Randomized, 2-Period Trial to Evaluate the Effect of HerpV Administered in Combination With the Stimulon® Adjuvant QS-21 on Viral Shedding in Adults With Recurrent Genital Herpes

Agenus Inc.·interventional·Posted Sep 19, 2012·Updated Jul 13, 2021

In Brief

A Phase 2 clinical trial evaluating HerpV and QS-21 and Placebo for Herpes Simplex Type 2. Completed, enrolled 80 participants across 5 sites.

Detailed Summary

The purpose of this study is to evaluate the effect of recombinant human heat shock protein 70-polyvalent peptide complex (HerpV) vaccine administration on recurring episodes of genital herpes by evaluating viral shedding before and after treatment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedSep 19, 2012
Enrollment StartOct 29, 2012
Primary CompletionSep 1, 2013
Study CompletionJan 1, 2015
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 13.8 years ago

Interventions

HerpV and QS-21drug

HerpV (recombinant human heat shock protein 70 \[rh-Hsc70\] polyvalent peptide complex) in combination with adjuvant QS-21

Placebodrug

phosphate buffered saline