Study of Tenofovir Disoproxil Fumarate (TDF) for Prevention of HIV

NCT ID: NCT00122512

Last Updated: 2006-02-10

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 500 participants
• Study Classification: INTERVENTIONAL

Brief Summary

This Phase 2a study involving Tenofovir Disoproxil Fumarate (TDF) will provide extended safety data for high-risk men. Secondarily, the study will assess the feasibility of conducting the trial and evaluate the preliminary effectiveness of TDF 300 mg as an HIV prevention method when taken once a day.

Detailed Description

TDF has been selected for investigation as prophylaxis against HIV in high-risk men because of its unique pharmacologic profile. In addition to the convenience of being a once daily single tablet, TDF's safety profile is comparable to placebo among HIV infected persons, it has striking anti-HIV potency, and it has low potential for selection of resistant viruses. TDF is cleared from the body by the kidneys and is not metabolized by the liver. Therefore, TDF has limited potential to have pharmacokinetic interactions with other hepatically metabolized drugs. Each of these properties is necessary given the realities of the intended target populations. Moreover, initial prevention studies in simian models have provided encouraging results. Finally, the drug's sponsor is supportive of investigating the potential use of TDF as a preventive, as well as therapeutic agent, will provide TDF for the study, and is willing to make a good faith effort to make TDF available for public health use should it prove to be effective for HIV prevention.

Conditions

HIV Infections

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: PREVENTION
• Blinding Strategy: DOUBLE

Interventions

Tenofovir Disoproxil Fumarate

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Be willing and able to give informed consent
• Be 18 years or older
• Be willing to use study product as directed
• Be willing to adhere to follow-up schedule
• Be willing to participate in the study for up to 12 months
• Be in general good health (no active, serious infections that require parenteral antibiotics, no active clinically significant medical conditions, including heart disease, diabetes, asthma, alcoholism, and cancer)
• Meet at least one of these three high risk criteria: *Sex with sex worker/bar girl in last 3 months;

• Sex with 2 or more women in last 3 months;
• Sexually transmitted disease (STD) in last 3 months
• Have absence of HIV antibodies by rapid test (at screening and enrollment visit)
• Have absence of hepatitis B (HB) surface antigen (sAg)
• Have adequate renal function (serum creatinine <1.5 mg/dL)
• Have adequate liver function (hepatic transaminases (ALT <54 U/L and AST<46 U/L)
• Have adequate serum phosphorus (>2.2 mg/dL)
• Not be intending to relocate out of the area for the duration of the study participation and does not have a job or other obligations that may require long absences from the area
• Not be receiving an experimental HIV vaccine

• Minimum Eligible Age: 18 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

FHI 360

OTHER

Sponsor Role: lead

Principal Investigators

Irving Hoffman, PA, MPH

Role: PRINCIPAL_INVESTIGATOR

UNC Center for Infectious Diseases

Locations

UNC Project, Kamuzu Central Hospital

Lilongwe, , Malawi

Countries

Malawi

Other Identifiers

9876

Identifier Type: -

Identifier Source: org_study_id