An Open-Label, Non-Randomized Trial to Evaluate the Tolerability and Safety of Viramune (Nevirapine) in Adult and Pediatric Patients With Progressive HIV Disease
Completed · Phase 3
Conditions studied: HIV Infections
In brief
To provide access to Viramune and to evaluate the tolerance and safety of Viramune in patients with progressive, symptomatic HIV disease who failed or are intolerant to currently approved treatment for HIV-1 infection and who are unable to participate in another Viramune controlled clinical trial and have a compelling need for anti-HIV treatment.
Key facts
- Study ID
- NCT00002166
- Run by
- Boehringer Ingelheim
- Last updated by the study team
- 2005-06-24
Who can join
Age: 0 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients must have:
- Patients > 18 months of age with history of positive serology for HIV-1 infection or patients <= 18 months of age with history of positive viral culture, detectable p24 antigen, or positive peripheral blood mononuclear cell macro culture.
- Patients >= 13 years of age with a CD4+ cell count <= 200 cells/mm3. Patients < 13 years of age with a CD4% <= 14% or a 50% decrease in CD4% in the past 6 months if the previous CD4% was >=20%.
- Patient has failed or is intolerant to currently approved treatments for HIV-1 infection and is unable to participate in a controlled viramune clinical trial.
- Written and informed consent from a parent or guardian for patients < 18 years of age.
- Patient or guardian is willing and able to follow protocol requirements. (PER AMENDMENT 1/29/97:
- Enrollment is closed to adults, as of Jan. 29th only pediatric patients will be enrolled.)
You may not qualify if…
- Co-existing Condition:
- Patients with the following symptoms and conditions are excluded:
- Patient qualifies for participation in an actively accruing Viramune controlled clinical trial.
- Concurrent Medication:
- Excluded:
- Dicumarol, Warfarin, and other anticoagulant medications.
- Tolbutamide.
- Investigational drugs, all protease inhibitors, and all other non-nucleoside transcriptase inhibitors.
- Neurotoxic drugs.
- Cimetidine.
- Erythromycin.
- Required:
- Patient has failed or is intolerant to currently approved treatments for HIV-1 infection.
Where it is running
- Boehringer Ingelheim Pharmaceuticals Inc — Ridgefield, Connecticut, United States
Full record on ClinicalTrials.gov
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