A Study of Delavirdine Used Together With Other Anti-HIV Drugs in HIV-Infected Patients
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|ClinicalTrials.gov Identifier: NCT00002401|
Recruitment Status : Completed
First Posted : August 31, 2001
Last Update Posted : June 24, 2005
|Condition or disease||Intervention/treatment||Phase|
|HIV Infections||Drug: Indinavir sulfate Drug: Delavirdine mesylate Drug: Lamivudine Drug: Zidovudine||Not Applicable|
In this open-label pilot study, patients are randomized to 1of the following 4 arms for 24 weeks:
Arm 1 (40 patients): DLV plus ZDV plus IDV. Arm 2 (40 patients): DLV plus IDV plus 3TC*. Arm 3 (40 patients): DLV plus ZDV plus IDV plus 3TC. Arm 4 (40 patients): ZDV plus IDV plus 3TC.
- Dose determined by body weight. Patients may opt to continue on study for 24 additional weeks at the discretion of the investigator.
|Study Type :||Interventional (Clinical Trial)|
|Enrollment :||160 participants|
|Official Title:||An Open-Label Randomized Study of Delavirdine Mesylate (DLV, Rescriptor) in Triple and Quadruple Combinations With Zidovudine (ZDV), Indinavir (IDV), and Lamivudine (3TC) in HIV-1 Infected Individuals|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00002401
|United States, New Jersey|
|Pharmacia & Upjohn|
|Peapack, New Jersey, United States, 07977|