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Completed No phase listed Observational

Case-Control Viramune (Nevirapine) Toxicogenomics Study

ClinicalTrials.gov ID: NCT00310843

Public ClinicalTrials.gov record NCT00310843. 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 Oct 30, 2026, 1:09 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 Case-Control Toxicogenomics Study to Identify Unique Genetic Polymorphisms in Patients Who Have Experienced Symptomatic Hepatotoxicity or Severe Cutaneous Toxicity Within the First 8 Weeks of Nevirapine Therapy

Brief summary

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

Attempt to identify genetic polymorphisms in interrogated pathways which may be associated with symptomatic hepatotoxicity or severe cutaneous toxicity observed in case patients within the first 8 weeks of nevirapine therapy.

Study identification

NCT ID
NCT00310843
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
889 participants

Conditions and interventions

Conditions

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
Feb 2006 (Type not available)
Primary completion
Sep 2008 (Actual)
Completion
Not listed
Last update posted
Aug 1, 2013

Started 2006

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
1100.1452.01006 Boehringer Ingelheim Investigational Site Birmingham Alabama — —
1100.1452.01013 Boehringer Ingelheim Investigational Site Denver Colorado — —
1100.1452.99999 Boehringer Ingelheim Investigational Site Baltimore Connecticut — —
1100.1452.01011 Boehringer Ingelheim Investigational Site New Haven Connecticut — —
1100.1452.01003 Boehringer Ingelheim Investigational Site Baltimore Maryland — —
1100.1452.01002 Boehringer Ingelheim Investigational Site Boston Massachusetts — —
1100.1452.01014 Boehringer Ingelheim Investigational Site Springfield Massachusetts — —
1100.1452.01015 Boehringer Ingelheim Investigational Site St Louis Missouri — —
1100.1452.01016 Boehringer Ingelheim Investigational Site New York New York — —
1100.1452.01012 Boehringer Ingelheim Investigational Site Chapel Hill North Carolina — —
1100.1452.01001 Boehringer Ingelheim Investigational Site Nashville Tennessee — —
1100.1452.01004 Boehringer Ingelheim Investigational Site Fort Worth Texas — —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 90 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00310843, 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 Aug 1, 2013 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00310843 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →