Clinical trial
Safety and Effectiveness of Giving an Anti-HIV Drug Combination of Adefovir…
NCT00002234 · Gilead Sciences, Industry · Completed
Key facts
| NCT number | NCT00002234 |
|---|---|
| Title | Safety and Effectiveness of Giving an Anti-HIV Drug Combination of Adefovir Dipivoxil Plus Didanosine Plus Efavirenz Plus Lamivudine Once Daily to HIV-Infected Patients |
| Official title | A Phase II, 48 Week, Open-Label Study Designed to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of a Simplified Dosing Regimen of Preveon (Adefovir Dipivoxil; bis-POM PMEA), Videx (Didanosine; ddI), Sustiva (Efavirenz; DMP-266), and Epivir (Lamivudine; 3TC) Administered Once… |
| Lead sponsor | Gilead Sciences, Industry |
| Collaborators | Bristol-Myers Squibb Industry Glaxo Wellcome Dupont Applied Biosciences |
| Status | Completed |
| Phase | Phase 2 |
| Study type | Interventional |
| Conditions | HIV Infections |
| Intervention type | Drug |
| Interventions | Efavirenz, Adefovir dipivoxil, Lamivudine, Didanosine |
| Enrollment | 25 |
| First posted | Aug 31, 2001 |
| Last update posted | Jun 24, 2005 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: