SWEET: Once Daily Truvada Versus Twice Daily Combivir for the Treatment of HIV Infection

NCT ID: NCT00323544

Last Updated: 2008-07-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 220 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-10-31
• Study Completion Date: 2007-10-31

Brief Summary

This study will investigate whether the simplified regimen of a once daily fixed dose combination of Truvada (emtricitabine and tenofovir disoproxil fumarate [DF]) will be associated with a reduced rate of adverse events, seen with long term use of antiretrovirals, as well as improved adherence compared to a twice daily fixed dose combination of Combivir.

Detailed Description

The success of HAART is largely dependant on an individual's ability to adhere strictly to an antiretroviral regimen. Regimen characteristics that affect adherence include dosing frequency and pill burden. Several studies have shown improved adherence with lower pill burden and a meta-analysis of the virological outcome in relation to pill burden has shown a significant correlation between lower pill burden and better virological outcome. A systematic review of studies across a range of medical specialties demonstrated that once daily therapy improves adherence relative to more frequent dosing although statistical significance was not demonstrated relative to twice daily regimens.

Conditions

HIV Infections

Keywords

HIV 1; HIV 1 infection

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Interventions

zidovudine and lamivudine (Combivir®)

Intervention Type: DRUG

emtricitabine and tenofovir DF

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Patients of either sex aged > 18 years.

2. HIV positive.

3. Stable antiretroviral therapy consisting of efavirenz (EFV) given with Combivir® or zidovudine (AZT) + lamivudine (3TC) for at least 6 months.

4. Patients with viral loads < 50 copies/ml on last 2 consecutive tests and < 400 copies/ml for > 3 months.

5. Patients requiring a lipid lowering agent must be established on a stable dose/frequency for at least 12 weeks prior to Baseline and be expected to continue on stable dose/frequency for the duration of the study.

6. Negative serum pregnancy test (females of childbearing potential only).

7. Willingness to use effective contraception (such as barrier or coil methods) by both males and females while on study treatment and for 30 days following study drug completion.

8. The ability to understand and sign a written informed consent form, which must be obtained prior to initiation of study procedures.

Exclusion Criteria

1. Pregnant or lactating female.

2. History of AZT monotherapy.

3. Use of anabolic steroids, with the exception of testosterone for documented hypogonadism, within 90 days prior to the Baseline visit.

4. Documented parvovirus infection.

5. Use of erythropoietin within the last six weeks.

6. Patients who have had a blood transfusion in the last six weeks.

7. Karnofsky score < 50.

8. Prior history of significant renal disease.

9. Prior history of osteopenia/osteoporosis.

10. Creatinine clearance < 60mL/min.

11. AST/ALT > 5 x upper limits of normal (ULN).

12. Previous adefovir dipivoxil or cidofovir therapy.

13. Known history of resistance (including primary resistance) to any of the study medications - tenofovir disoproxil fumarate (TDF), emtricitabine (FTC), AZT, 3TC, or EFV.

14. Patients receiving ongoing therapy with any of the following (administration of any of the following medications must be discontinued at least 30 days prior to the Baseline visit and for the duration of the study period):

• Nephrotoxic agents
• Probenecid
• Systemic chemotherapeutic agents (i.e. cancer treatment medications)
• Systemic corticosteroids
• Interleukin 2 (IL 2)
• Drugs that interact with efavirenz
• Dihydroergotamine
• Ergotamine
• Midazolam
• Triazolam
• Cisapride
• Rifampin
• Ergonovine
• Methylergonovine

15. Patients with known hypersensitivity to any of the study medications or excipients.

16. Active, serious infections (other than HIV-1 infection) requiring parenteral antibiotic therapy within 15 days prior to Screening.

17. Patients who are currently taking part in any other clinical trial or have taken part in a clinical trial of a new chemical entity within 1 month prior to Screening.

18. Any other clinical condition or prior therapy that, in the opinion of the investigator, would make the patient unsuitable for the study or unable to comply with the dosing requirements.

19. Patients with cancer (except basal cell carcinoma).

20. Co-infection with hepatitis B virus

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Gilead Sciences

INDUSTRY

Sponsor Role: lead

Responsible Party

Gilead Sciences

Principal Investigators

Claudio Avila, MD

Role: STUDY_DIRECTOR

Gilead Sciences, Ltd.

Locations

Gilead Sciences

Cambridge, , United Kingdom

Countries

United Kingdom

References

Fisher M, Moyle GJ, Shahmanesh M, Orkin C, Kingston M, Wilkins E, Ewan J, Liu H, Ebrahimi R, Reilly G; SWEET (Simplification With Easier Emtricitabine Tenofovir) group UK. A randomized comparative trial of continued zidovudine/lamivudine or replacement with tenofovir disoproxil fumarate/emtricitabine in efavirenz-treated HIV-1-infected individuals. J Acquir Immune Defic Syndr. 2009 Aug 15;51(5):562-8. doi: 10.1097/QAI.0b013e3181ae2eb9.

Reference Type: DERIVED

PMID: 19561519 (View on PubMed)

Related Links

http://www.gileadclinicaltrials.com/pdf/GS-MC-164-011_Synopsis_Public%20Disclosure_Final.pdf

Study Results

Other Identifiers

GS-MC-164-0111

Identifier Type: -

Identifier Source: org_study_id