A Pilot Study of LTB4 in HIV-1 Infected Adults

LTB4 Sweden

Status and phase: Completed; Phase 2

Conditions: HIV Infections

Treatments: Drug: LTB4

Study type: Interventional

Funder types: Industry

Identifiers

NCT00251537

LTB4 200501

Details and patient eligibility

About

This is a pilot study to assess the safety and antiretroviral activity of a naturally occuring substance known as Leukotriene B4(LTB4). The aim of the study is to determine the effect of LTB4 on viral load during a period of 6 weeks, 4 weeks of active treatment and 2 additional weeks after the end of active treatment for safety follow-up. 40 patients in seven clinics in Canada will be randomized into three treatment arms, either of two doses of LTB4 or placebo. Study drug is administered intravenously once daily. LTB4 can activate and stimulate various white blood cells and by the activation release natural substances in the body and this process is an important part of the body's defense against infections.

Full description

The objective of this pilot study is to investigate whether LTB4, administered at a dose that provides an increase in alfa-defensin release from neutrophils, can affect HIV viral load in HIV-1 infected individuals. The safety, tolerability and effect will be assessed of 28 days of daily intravenous dosing of LTB4 on HIV viral load. Safety and tolerability will also be assessed.

The study is randomized, double-blind, placebo controlled. All subjects will be randomly assigned to one of three treamtent groups, LTB4 at two different dose levels or corresponding placebo. Treatment duration is 4 weeks and follow-up period is 2 weeks. Subjects will visit the clinic on a daily basis during the treatment period to receive a daily intravenous injection of the study drug. 40 subjects will be enrolled, seven clinics in Canada will participate in the study.

Primary endpoint: Change in viral load over the treatment period of 28 days. Secondary endpoint: CD4, CD8 and neutrophil counts, alfa-defensins and CC-che, mokine release in blood.

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Male and female subjects between 18 and 65 years of age
2. Diagnosis of HIV-1 infection
3. Plasma HIV RNA level greater or equal to 5,000 copies/mL at the screening visit
4. A CD4 cell count equal or greater than 250 cells/mm3 and CD4 fraction equal or greater than 14% at the screening visit within one month of study entry
5. No ART within two months of study entry
6. Karnofsky score equal to or above 80
7. If female of childbearing potential, a negative serum pregnancy test at screening.
8. In the opinion of the investigator, the subject will be able to comply with the requirements of the protocol, including ability to present for all required visits
9. Subject is capable of understanding and signing an informed consent form

Exclusion criteria

1. Primary HIV-1 infection
2. Use of investigational therapy in the preceding month prior to screening visit
3. Prior screening for entry into this study
4. Use of G-CSF, GM-CSF, IL-2, IFNs, erythropoietin, systemic or inhaled steroids within one month of the screening visit
5. HIV-vaccine within one year of the screening visit
6. Concurrent disease or conditions that may present a risk to the subjects
7. Females who are pregnant or breast feeding
8. History of any malignancy or any active malignancy, except cutaneous Kaposis sarcoma
9. Unexplained temperature of 38.5 degrees Celsius
10. Chronic diarrhea (>3 liquid stools per day persisting for 15 days) within one month prior to study entry
11. Calculated creatinine clearance outside normal limits
12. Urinalysis: hemoglobinuria, present
13. Liver transaminases > 3 x ULN
14. Absolute neutrophil count < 500/mm3
15. Hemoglobin < 8.0g/dL
16. Platelet count < 75,000/mm3

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind