Open-Label Study Comparing Efficacy and Safety of ATV/RTV+3TC With ATV/RTV+TDF/FTC in HIV-Infected, Treatment Naïve Subjects, Followed by Treatment With ATV/RTV+3TC

NCT ID: NCT01620944

Last Updated: 2024-01-10

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE3
• Total Enrollment: 3 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-07-31
• Study Completion Date: 2013-01-22

Brief Summary

The primary objective of this study in antiretroviral (ARV)-naïve Human immunodeficiency virus 1 (HIV-1) ribonucleic acid infected subjects is to compare the response rate at Week 48 of a daily regimen of Atazanavir (ATV)/ Ritonavir (RTV)HS 300/100 mg combined with either one additional drug [Lamivudine (3TC) 300 mg daily] or 2 additional drugs [Tenofovir/Emtricitabine(TDF/FTC) 300/200 mg daily].

Conditions

HIV

Study Design

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

Study Groups

Arm1: ATV/RTVHS+3TC

Group Type: EXPERIMENTAL

Atazanavir

Intervention Type: DRUG

Capsule, oral, 300 mg, Once daily (QD), 96 weeks

Ritonavir

Intervention Type: DRUG

Tablets, oral, 100 mg, QD, 96 Weeks

Lamivudine

Intervention Type: DRUG

Tablet, oral, 300 mg, QD, 96 Weeks

Arm2: ATV/RTVHS+TDF/FTC

Group Type: ACTIVE_COMPARATOR

Atazanavir

Intervention Type: DRUG

Capsule, oral, 300 mg, Once daily (QD), 96 weeks

Ritonavir

Intervention Type: DRUG

Tablets, oral, 100 mg, QD, 96 Weeks

Tenofovir/Emtricitabine

Intervention Type: DRUG

Tablets, oral, 300/200 mg, QD, 48 Weeks

Interventions

Atazanavir

Capsule, oral, 300 mg, Once daily (QD), 96 weeks

Intervention Type: DRUG

Ritonavir

Tablets, oral, 100 mg, QD, 96 Weeks

Intervention Type: DRUG

Lamivudine

Tablet, oral, 300 mg, QD, 96 Weeks

Intervention Type: DRUG

Tenofovir/Emtricitabine

Tablets, oral, 300/200 mg, QD, 48 Weeks

Intervention Type: DRUG

Other Intervention Names

Ritonavir high sensitivity (RTV HS)

Eligibility Criteria

Inclusion Criteria

• Signed Written Informed Consent.

i) Freely given informed consent must be obtained from subjects prior to clinical trial participation, including informed consent for any screening procedures conducted to establish subject eligibility for the trial.

ii) A freely given Pharmacokinetics (PK) sub-study consent form must be obtained from the subset of subjects participating in the intensive PK sub-study.

• Target Population.

i) Treatment-naive HIV-1-infected subjects (< 48 hours of any ARV is allowed).

ii) Subjects who have an HIV-1 Ribonucleic acid (RNA) level ≥ 1000 c/mL at screening.

iii) Subjects who have a Antigenic marker of helper/inducer T lymphocytes (CD4) + cell count > 100 cells/mm3.

• Age and Reproductive Status.

i) Men and women, 18 years of age or older (or minimum age as determined by local regulatory or legal requirements).

ii) Women of childbearing potential (WOCBP) must use highly effective methods of birth control for up to 8 weeks after the last dose of investigational product to minimize the risk of pregnancy. WOCBP must follow instructions for birth control for the entire duration of the study including a minimum of 30 days after dosing has been completed.

iii) Acceptable methods of highly effective birth control include:.

A. Condom with spermicide.

B. Diaphragm and spermicide.

C. Cervical cap and spermicide

• Since acceptable and available methods of contraception vary among different countries, participating women may choose their preferred contraceptive method atazanavir AI424494 BMS-232632 Clinical Protocol Date: 31-01-2012 33 based on physician recommendations. Caution is warranted with co-administration of oral contraceptives (ethinyl estradiol and norethindrone).

i) Women must have a negative serum or urine pregnancy test [minimum sensitivity 25 IU/L or equivalent units of Human chorionic gonadotropin (HCG)] within 24 hours prior to the start of investigational product.

ii) Women must not be breastfeeding.

iii) Sexually active fertile men must use highly effective birth control if their partners are WOCBP.

Exclusion Criteria

• Target Disease Exceptions.

i) Subjects who have an HIV-1 RNA level ≥500,000 c/mL at screening.

ii) Screening HIV genotype showing resistance to any component of the study regimen (ATV, RTV, 3TC, TDF/FTC).

iii) Previously documented HIV-2 infection.

• Medical History and Concurrent Diseases.

i) Acute or chronic hepatitis B virus (HBV) or Acute hepatitis C virus (HCV) co-infection.

i) Presence of a newly diagnosed HIV-related opportunistic infection (OI) or any medical condition requiring acute therapy at the time of enrollment. Subjects on stable maintenance therapy for an OI may be enrolled.

ii) Primary HIV infection.

iii) History or current cardiac disease, defined by presence of arrhythmias, ischemic disease, or a conduction abnormality including left bundle branch block (LBB) or left anterior fascicular block (LAFB), 2nd or 3rd-degree atrioventricular block (AVB), or any cardiac abnormality deemed clinically significant by the investigator. In addition, the following Electrocardiogram (ECG) findings are exclusionary:.

A. PR Interval > 260 msec (severe 1st degree AV Block).

B. QRS Interval > 120 msec.

iv) Moderate-to-severe hepatic insufficiency.

v) Obstructive liver disease.

vi) Recent therapy with agents having significant systemic myelosuppressive, neurotoxic, pancreatotoxic, hepatotoxic or cytotoxic potential within 3 months of study start or the expected need for such therapy at the time of enrollment, or therapy with methadone or ribavirin/interferons or treatment with neurotoxic drugs or drugs that affect CYP3A4.

vii) Concomitant administration of a proton pump inhibitor (PPI) or H2 blocker or any other drug with potential interaction with the investigational products.

viii) Life expectancy < 1 year according to the judgment of the investigator.

ix) Active alcohol or substance use sufficient, in the investigator's opinion, to prevent adequate compliance with study therapy or to increase the risk of developing pancreatitis or chemical hepatitis.

x) History or ongoing psychiatry disorder.

xi) Any other clinical conditions or prior therapy that, in the opinion of the investigator, would make the subject unsuitable for study or unable to comply with the dosing requirements.

• Physical and Laboratory Test Findings.

i) Screening laboratory analysis shows any of the following abnormal laboratory results:.

A. Grade IV glucose.

B. Grade IV electrolytes.

C. Grade IV transaminases.

D. Grade IV hematology.

ii) Calculated creatinine clearance < 60 mL/min as estimated by the Cockcroft-Gault equation.

• Allergies and Adverse Drug Reaction.

i) Hypersensitivity to any component of the study drug formulations.

• Sex and Reproductive Status.

i) Pregnancy.

i) Prisoners or subjects who are involuntarily incarcerated.

ii) Subjects who are compulsorily detained for treatment of either a psychiatric or physical (eg, infectious disease) illness.

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

Sponsors

Bristol-Myers Squibb

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Bristol-Myers Squibb

Role: STUDY_DIRECTOR

Bristol-Myers Squibb

Related Links

http://bms.com/studyconnect/Pages/home.aspx

BMS Clinical Trial Patient Recruiting

http://www.bms.com/clinical_trials/Pages/Investigator_inquiry_form.aspx

Investigator Inquiry Form

Other Identifiers

2011-006187-47

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

AI424-494

Identifier Type: -

Identifier Source: org_study_id