Withdrawn

Phase 2
Age: 13Years +
All Genders
ID00001094

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

Age: 13Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

This study has been terminated.

Not Eligible

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

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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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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 | DecenTrialz