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Completed Phase 2 Interventional

A Study With ASP2151 in Subjects With Recurrent Episodes of Genital Herpes

ClinicalTrials.gov ID: NCT00486200

Public ClinicalTrials.gov record NCT00486200. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 11:29 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase II, Dose-Finding Study With ASP2151 in Subjects With Recurrent Episodes of Genital HErpes

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A study of ASP2151 in subjects with recurrent outbreaks of genital herpes.

Study identification

NCT ID
NCT00486200
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Astellas Pharma Inc
Industry
Enrollment
695 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 20, 2007
Primary completion
Aug 11, 2008
Completion
Aug 11, 2008
Last update posted
Dec 6, 2017

2007 – 2008

United States locations

U.S. sites
25
U.S. states
18
U.S. cities
24
Facility City State ZIP Site status
Not listed Birmingham Alabama 35294
Not listed Phoenix Arizona 85015
Not listed Tucson Arizona 85712
Not listed Los Angeles California 90017
Not listed Sacramento California 95821
Not listed San Diego California 92108
Not listed Westlake Village California 91361
Not listed Denver Colorado 80262
Not listed Boynton Beach Florida 33472
Not listed Miami Florida 33156
Not listed Atlanta Georgia 30328
Not listed Indianapolis Indiana 46202
Not listed Madisonville Kentucky 42431
Not listed Baltimore Maryland 21201
Not listed Billings Montana 59101
Not listed Omaha Nebraska 68134
Not listed Albuquerque New Mexico 87131
Not listed Portland Oregon 97210
Not listed Philadelphia Pennsylvania 19103
Not listed Arlington Texas 76011
Not listed Houston Texas 77030
Not listed Houston Texas 77058
Not listed Salt Lake City Utah 84132
Not listed Annandale Virginia 22003
Not listed Seattle Washington 98122

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00486200, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 6, 2017 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00486200 live on ClinicalTrials.gov.

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