Completed

Thymopentin's Effect on HIV-1 Infectivity and Immune System in HIV Patients

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What is being tested

Thymopentin

Drug
Who is being recruted

Blood-Borne Infections+14

+ Urogenital Diseases

+ Genital Diseases

Over 18 Years
+15 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
See protocol details

Summary

Principal SponsorImmunobiology Research Institute
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

This study focuses on HIV-infected patients who have not yet developed AIDS. The main goal is to investigate how a drug called Timunox, also known as thymopentin, can potentially reduce the amount and frequency of the HIV virus found in the blood and semen. The study also aims to understand if thymopentin can boost the immune system and bring about changes in the clinical findings of these patients, which could improve their overall health and quality of life.

NCT00002289
Principal SponsorImmunobiology Research Institute
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Blood-Borne InfectionsUrogenital DiseasesGenital DiseasesCommunicable DiseasesImmunologic Deficiency SyndromesImmune System DiseasesInfectionsRetroviridae InfectionsRNA Virus InfectionsSexually Transmitted DiseasesSlow Virus DiseasesVirus DiseasesSexually Transmitted Diseases, ViralLentivirus InfectionsAIDS-Related ComplexHIV SeropositivityHIV Infections

Criteria

6 inclusion criteria required to participate
Allowed concurrent medication: Aerosolized pentamidine

Allowed prior medication: Aerosolized pentamidine

HIV-1 p24 antigen must be detected in supernatant fluids from co-cultures of patients' peripheral blood monocytes (PBMC) on two separate occasions

Patients with HIV "wasting syndrome" are allowed

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9 exclusion criteria prevent from participating
Immunomodulatory or experimental therapy within 30 days of study entry

Intravenous drug abuse

Patients with AIDS as defined by the CDC

Patients with abnormal chest x-ray (indicative of active disease (opportunistic infection)) within 30 days prior to study entry

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Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Immunobiology Research Institute

Annandale, United StatesOpen Immunobiology Research Institute in Google Maps
CompletedOne Study Center