Evaluation of the Immune Response of a HIV Candidate Vaccine After Administration of One Chloroquine Dose

GlaxoSmithKline28 enrolled

Overview

The purpose of this study is to evaluate the safety and reactogenicity of one booster dose of a HIV candidate vaccine after administration of one oral dose of chloroquine.

The Protocol Posting has been updated following Protocol amendment 1, October 2009.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

NONE

Enrollment

Conditions

AIDS

Interventions

GSK Biologicals' HIV vaccine (732461)BIOLOGICAL

1 dose intramuscular injection

ChloroquineDRUG

One dose of 300 mg

Eligibility

Sex: ALLMin age: 18 YearsMax age: 52 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * A male or female between, and including, 18 to 52 years of age at the time of vaccination. * Written informed consent prior to any study related procedure on the subject. * Subjects who the investigator believes that they can and will comply with the requirements of the protocol. * Good general health without significant medical history or physical examination findings. * Negative for anti-HBc and anti-Hepatitis C Virus antibodies. * Female subjects of non-childbearing potential may be enrolled in the study. * Female subjects of childbearing potential may be enrolled in the study, if the subject: * has practiced adequate contraception for 30 days prior to vaccination, and * has a negative pregnancy test on the day of vaccination, and * has agreed to continue adequate contraception until study completion. * Previous participation and completion of the study NCT00434512. * Cellular and humoral immune responder to vaccines administered in study NCT00434512. * Subjects must be willing to accept HIV test results. Individuals who elect not to receive test results will not be enrolled. Exclusion Criteria: * Clinically significant laboratory value above normal range for blood urea nitrogen, creatinine, alanine aminotransferase and aspartate aminotransferase, or clinically significant laboratory value above or below normal range for Hemoglobin, as per investigator judgment. * Women who are pregnant or breast-feeding. * Receipt of live attenuated vaccines within 30 days of vaccination. * Receipt of medically indicated subunit or killed vaccines (e.g., influenza, pneumococcal) or allergy treatment with antigen injections (including a tuberculin skin test) within \<= 21days preceding and planned \<= 21 days following the study vaccine administration. * Receipt of blood products 120 days prior to vaccination. * Receipt of immunoglobulin 120 days prior to vaccination. * Subject has donated blood in the last 3 months. * Bleeding disorder that was diagnosed by a physician; e.g., factor deficiency, coagulopathy or platelet disorder that requires special precautions. * Chronic administration of immunosuppressants or other immune-modifying drugs within six months prior to the first. * History of serious adverse reactions to vaccines including anaphylaxis and related symptoms such as hives, respiratory difficulty, angioedema and abdominal pain. * History of any reaction or hypersensitivity likely to be exacerbated by any component of the vaccine/product. * History of serious allergic reaction to any substance requiring hospitalization or emergency medical care. * History of hypersensitivity against chloroquine or any components of the drug. * History of hypersensitivity against aminoglycosides. * Ophthalmologic findings at screening. * Previous administration of 4-aminoquinoline in the previous year or for a duration of more than 1 year. * History of Glucose-6-Phosphate Dehydrogenase deficiency. * History of hematopoietic disease. * History of Myasthenia gravis. * History of any serious neurological disorder or seizure. * History of immunodeficiency or immune-mediated disorders, including active psoriasis. * History of type I or type II diabetes mellitus including cases controlled with diet alone. * Thyroid disease including history of thyroidectomy and diagnoses requiring medication. * Asthma requiring daily steroid or long acting β-agonist prevention. * Unstable asthma defined as: * Sudden acute attacks occurring in less than three hours without an obvious trigger. * Hospitalization for asthma in the last two years. * Food- or wine-induced asthma. * Known sensitivity to sulfites or aspirin. * History of major congenital defect. * History of chronic fatigue syndrome or fibromyalgia. * History of malignancy. * Splenectomy. * Morbid obesity. * Clinically relevant hypertension. * Subjects with a history of, or current, alcohol or substance abuse. * Use of any investigational or non-registered product other than the study vaccines within 30 days preceding the first dose of study vaccines, or planned use during the study period. * Concurrently participating in another clinical study, at any time during the study period, in which the subject has been or will be exposed to an investigational or a non-investigational product (pharmaceutical product or device). * Previous inclusion in a HIV vaccines trial other than study NCT00434512. * Subject is seropositive for HIV, as determined by the test results performed.

Locations (1)

GSK Investigational Site

Ghent, Belgium

Outcomes

Primary Outcomes

Number of Subjects With Frequency of Cluster of Differentiation 8 (CD8+) T Cells Expressing at Least One Cytokine to at Least 1, 2, 3 or All 4 Antigens

Among expressed cytokines were interleukin-2 (IL-2), tumour necrosis factor alpha (TNF-α) and interferon gamma (INF-γ), as determined by intracellular cytokine staining (ICS).

Time frame: At Day 14

Number of Subjects With Solicited Local Symptoms

Assessed solicited local symptoms were pain, redness and swelling. Any = occurrence of the symptom regardless of intensity grade. Grade 3 pain = pain that prevented normal activity. Grade 3 redness/swelling = redness/swelling spreading beyond 50 millimeters (mm) of injection site.

Time frame: During the 7 Day (Days 0-6) post-vaccination period

Number of Subjects With Solicited General Symptoms

Assessed solicited general symptoms were fatigue, temperature \[defined as axillary temperature equal to or above 37.5 degrees Celsius (°C)\], gastrointestinal symptoms \[nausea, vomiting, diarrhoea and/or abdominal pain\] and headache. Any = occurrence of the symptom regardless of intensity grade. Grade 3 symptom = symptom that prevented normal activity. Grade 3 fever = fever \> 39.0 °C. Related = symptom assessed by the investigator as related to the vaccination.

Time frame: During the 7 Day (Days 0-6) post-vaccination period

Number of Subjects With Unsolicited Adverse Events (AEs)

An unsolicited AE covers any untoward medical occurrence in a clinical investigation subject temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product and reported in addition to those solicited during the clinical study and any solicited symptom with onset out-side the specified period of follow-up for solicited symptoms. Any was defined as the occurrence of any unsolicited AE regardless of intensity grade or relation to vaccination. Grade 3 AE = an AE which prevented normal, everyday activities. Related = AE assessed by the investigator as related to the vaccination.

Time frame: During the 32 Day (Days 2-29) post-chloroquine administration and during the 30 Day (Days 0-29) post-vaccine administration period

Data from ClinicalTrials.gov

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Secondary Outcomes

Magnitude of Antigen Specific CD8+ T Cells Expressing at Least One Cytokine

Magnitude was defined as the frequency of CD8+ T cells group-specific antigen (Gag) proteins 17, 24; negative regulatory factor (Nef); reverse transcriptase (RT) and fusion protein of all 4 antigens (F4co). Determination of F4co was done by stimulating the F4 antigen with a peptide pool spanning (pool\_F4co) or by adding individual frequencies of the CD8+ T cell response to each of the 4 antigens (F4co\_est). Among the cytokines expressed were IL-2, TNF-α and INF-γ.