Withdrawn
A Phase II, Randomized, Controlled, Open-Label Trial of Combination Therapy With Nelfinavir (NFV) and Saquinavir (SQV)Sgc With Delavirdine (DLV) or 3TC/ZDV Versus Nelfinavir (NFV) and 3TC/ZDV in Subjects With HIV Infection and > 5,000 HIV RNA Copies/ML
Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2015-03-09
N/A
Participants Needed
17
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
To compare the long-term virologic response to combination therapy with two protease inhibitors, i.e., nelfinavir (NFV) + saquinavir soft gel capsule (SQVsgc) and delavirdine (DLV) or combination lamivudine/zidovudine (3TC/ZDV, Combivir) versus NFV and 3TC/ZDV, in the proportion of patients demonstrating virologic success (\< 500 copies/ml HIV RNA) at week 48, without prior virologic or clinical failure. To evaluate the safety and tolerance of combination protease inhibitors. To evaluate the durability of virologic response as assessed by the Roche Ultra Sensitive assay (\< 200 copies/ml) and culturable virus. To compare time to a confirmed virologic response (two consecutive plasma HIV RNA levels \< 500 copies/ml) or to a confirmed treatment relapse following a confirmed virologic response across the treatment arms. To evaluate biologic phenotype (non-syncytium inducing versus syncytium inducing capacity) and the evolution and patterns of viral resistance among patients with confirmed treatment failures at or after weeks 16 to 24. To compare immunologic benefits, as measured by longitudinal CD4/CD8 cell count profiles. To evaluate the influence of baseline virologic and immunologic parameters on the magnitude and duration of plasma HIV RNA response. To compare virologic response between the two dose schedules of NFV and SQVsgc (bid vs tid) and between NFV and SQVsgc with either DLV or combination 3TC/ZDV. To evaluate compliance and exploratory population pharmacometrics. Past studies have shown that combination therapies not only will result in better clinical outcomes but may prolong the effects of therapy. The enhanced effects seen with combination therapies are likely related to a greater suppression of HIV replication and alterations in resistance patterns. Both in vitro and in vivo studies suggest that triple-drug therapy may have an advantage over one- and two-drug regimens. Therefore, triple-drug therapy appears to be an important strategy in the treatment of HIV infection.
CONDITIONS
Official Title
A Comparison of Nelfinavir Plus Saquinavir Plus Delavirdine or 3TC/ZDV Versus Nelfinavir Plus 3TC/ZDV in HIV-Infected Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
This study has been terminated.
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
Trial Site Locations
Total: 17 locations
1
Willow Clinic
Menlo Park, California, United States, 94025
Status Unknown
2
Stanford Univ Med Ctr
Stanford, California, United States, 943055107
Status Unknown
3
Univ of Colorado Health Sciences Ctr
Denver, Colorado, United States, 80262
Status Unknown
4
Univ of Miami School of Medicine
Miami, Florida, United States, 331361013
Status Unknown
5
Emory Univ
Atlanta, Georgia, United States, 30308
Status Unknown
6
Queens Med Ctr
Honolulu, Hawaii, United States, 96816
Status Unknown
7
Univ of Hawaii
Honolulu, Hawaii, United States, 96816
Status Unknown
8
Louis A Weiss Memorial Hosp
Chicago, Illinois, United States, 60640
Status Unknown
9
Tulane Univ School of Medicine
New Orleans, Louisiana, United States, 70112
Status Unknown
10
SUNY / Erie County Med Ctr at Buffalo
Buffalo, New York, United States, 14215
Status Unknown
11
Bellevue Hosp / New York Univ Med Ctr
New York, New York, United States, 10016
Status Unknown
12
Carolinas Med Ctr
Charlotte, North Carolina, United States, 28203
Status Unknown
13
Moses H Cone Memorial Hosp
Greensboro, North Carolina, United States, 27401
Status Unknown
14
Univ of Cincinnati
Cincinnati, Ohio, United States, 452670405
Status Unknown
15
Ohio State Univ Hosp Clinic
Columbus, Ohio, United States, 432101228
Status Unknown
16
Univ of Texas Galveston
Galveston, Texas, United States, 775550435
Status Unknown
17
Univ of Puerto Rico
San Juan, Puerto Rico, 009365067
Status Unknown
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
N/A
Model
N/A
Primary Purpose
TREATMENT
Number of Arms
0
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