Safety and Efficacy of ADAPTAVIR's Ability to Eliminate Treatment-Resistant Infectious Virus in Peripheral Blood Mononuclear Cells (PBMCs)

Status unconfirmed · Phase 2 · Has a placebo group

Conditions studied: HIV Infections

In brief

This is a 24 week placebo controlled, double-blind, 2-arm study of ADAPTAVIR, Monomeric Dala1-peptide T-amide (mDAPTA) compared to placebo, in HIV infected individuals with suppressed plasma viral loads \< 200 copies/ml by highly active antiretroviral therapy (HAART) treatment for at least 3 months prior to entry with at least 6 continuous months of HAART treatment preceding entry. 20 treatment and 20 placebo individuals will be enrolled in each arm. The study duration is 24 weeks on placebo or mDAPTA administered intranasally at 0.01 mg two times a day. The main (intent to treat) analysis is planned for the 24 week endpoint. The virological outcomes of interest in the present study are infectious virus recoverable from cellular (PBMC) sources and cellular viral mRNA and DNA copy numbers. Immune outcomes (plasma cytokines) associated with HIV disease, HIV replication, or immune function will be studied.

Key facts

Study ID

NCT00951743

Run by

Rapid Laboratories Inc.

People needed

40

Starts

2009-07-01

Expected to finish

2010-07-01

Last updated by the study team

2009-08-11

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• HIV positive, male or female of any race and at least 18 years of age.
• Must have received continuous currently acceptable anti-retroviral therapy ("HAART"; highly active antiviral therapy) for at least six months prior to entry.
• Must have HIV-1 plasma viral load RNA (PCR or bDNA) < 200 copies/mL for 90 days prior to randomization in this study.
• Women of childbearing potential must have a negative pregnancy test at screening prior to randomization in this study. Upon randomization, these women must agree to use methods of birth control or abstinence to prevent pregnancy.
• Must have a sustained CD4+ cell count > 350 cells/mm3 for 90 days prior to randomization in this study.
• Must be considered clinically stable, in the opinion of the investigator, at the time of entry into the study.

You may not qualify if…

• Expected to require adjustment to their antiretroviral therapy during screening or within 8 weeks after initiating mDAPTA therapy.
• Current participation in other clinical trials with investigational drugs.
• Use of any investigational agents including immunomodulatory agents (GM CSF, interferon, interleukin etc.) within 60 days prior to study entry.
• Use of any vaccine, including for Influenza (killed or live), Pneumovax etc., within 60 days of initiating therapy with mDAPTA.
• Use or anticipated use of immunosuppressive therapy, including chemotherapy during participation in the study.
• Alcohol or substance abuse which, in the opinion of the investigator, would interfere with patient compliance or safety.
• Study participants with an active opportunistic infection or malignancy.
• Pregnant or breastfeeding.
• Any condition or history of any illness which, in the opinion of the investigator, might confound the results of the study or pose additional risk in administering the study drugs to the participant.
• Participants who previously received treatment with DAPTA.

Where it is running

• Whitman Walker Clinic — Washington D.C., District of Columbia, United States (enrolling)

Full record on ClinicalTrials.gov

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