RAL+ATV/r in Comparison With TDF/FTC (or 3TC) +ATV/r in HIV Infected Patients

Chronic Infection With HIV Clinical Trial

— ARTE  

Official title:

A Pilot Randomized, Open Label Study to Evaluate Efficacy and Safety of the Combination of RAL+ATV/r in Comparison With TDF/FTC+ATV/r in HIV Infected Patients, Who Failed an Initial NNRTI Containing Regimen

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT01829802
• Other study ID #: FH-14
• Secondary ID: 50250
• Status: Active, not recruiting
• Phase: Phase 4
• First received: April 8, 2013
• Last updated: January 23, 2017
• Start date: May 2014
• Est. completion date: October 2017

Study information

• Verified date: January 2017
• Source: The Huesped Foundation
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this pilot study is to assess the efficacy and safety of the combination of RAL+ATV/r in comparison with TDF/FTC+ATV/r in HIV-1 infected patients presenting virologic failure and PI and TDF naïve.

Description:

Overall Study Design and Plan: Description

This is a pilot, randomized, open-label study. All the participants will be assigned to receive RAL+ATV/r or TDF/FTC+ATV/r. Patients will be evaluated at screening, randomization (day 0), and on weeks 4, 8, 12, 24, 36 and 48.

At the screening visit, subjects must be willing and able to give written (signed and dated) informed consent prior to any study specific procedures. They will receive a unique screening number and will undergo the study procedures associated with the screening visit. The investigator will evaluate whether the subject meets all eligibility criteria specified and record the details of the informed consent process and the results of this assessment in the subject's medical records. Two forms of the ICF will be signed, one for the subject and the other to file at the site.

At baseline visit, enrollment criteria will be reviewed and subjects who meet all of them will undergo study procedures. Subjects will receive instructions about study medications and dosing schedule. Subjects should start study medication within 24 hours of the baseline visit. Subjects will return to the investigator´s site for study visits and procedures. Subjects who prematurely discontinue the study must return for a discontinuation visit and undergo the study procedures identified for the discontinuation visit.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 50
• Est. completion date: October 2017
• Est. primary completion date: October 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female subject =18 years of age.

• Documented HIV-1 infection defined as a positive ELISA plus a confirmatory Western Blot; or a plasma HIV-1 RNA =10,000 copies/mL ever documented.

• Patients who have failed their initial treatment containing NNRTI(s) + 2NRTI(s) combination therapy, according to virological criteria defined by two consecutive (at least 7 days apart) HIV-1 RNA results =500 copies/mL. Subject must be on stable HAART for at least the last 4 weeks.

• No prior or current exposure to HIV-1 protease inhibitors and/or HIV-1 integrase inhibitors.

• Subject must have susceptibility to ATV/r and TDF, as resulted by resistance testing at screening. RAL sensitivity is not required for patients never exposed to this drug in the country.

• Subject has voluntarily signed ICF.

• Subject can comply with protocol requirements.

• Subject's general medical condition, in the investigator's opinion, does not interfere with assessments and completion of the trial.

• Subject agrees not to take any medication during the study, including over the counter medicines or herbal preparations, without the approval of the trial physician.

• If female, is not breastfeeding or pregnant.

• If female, subject must be either postmenopausal for at least one year, surgically sterile (bilateral tubal ligation, bilateral oophorectomy or hysterectomy), or she must use 2 different methods of birth control including, at least, one barrier method, that are acceptable to both the subject and investigator, and willing to continue their use for at least 30 days after the end of the treatment period.

• Subjects must have a life-expectancy of more than 1 year.

Exclusion Criteria:

• Patient has a current (active) diagnosis of acute hepatitis due to any cause OR chronic hepatitis B and/or C WITH aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) >2.5 x upper limit of normal (ULN) AND/OR is likely to require hepatitis treatment in the next year.

• Active hepatitis B infection (positive HBsAg), regardless of stage of infection.

• Subject has a currently active AIDS defining illness (Category C conditions according to the CDC Classification System for HIV infection 1993) in the last 30 days.

• Subjects with a laboratory abnormality Grade 3 or 4 with the following exceptions:

pancreatic amylase, cholesterol, triglycerides, gamma glutamyl transpeptidase.

• Screening laboratory analysis show any of the following abnormal results:

• Hemoglobin <8.0 g/dL

• Absolute neutrophil count <750 cells/µL

• Platelet count <50,000 mm3

• Creatinine >1.5 x ULN

• Any condition that, in the investigators opinion, could compromise the subject's safety or adherence to the trial protocol.

• The use of any study agent within 30 days prior to screening.

• Use of immunosuppressive drugs, cytokines inhibitors or other cytokines in the previous year.

• Any other condition (including, without limitation, the use of alcohol or drugs) that in the investigator's opinion may compromise the safety of the patient or his/her adherence to the protocol.

Related Conditions & MeSH terms

• Chronic Infection With HIV
• HIV Infections

Intervention

Drug:
• Ritonavir boosted Atazanavir
Ritonavir boosted Atazanavir 300/100 mg QD in combination with other drugs
• Raltegravir
Raltegravir 400 BID in combination with Ritonavir boosted Atazanavir 300/100 mg QD during 48 weeks
• TDF/FTC (or 3TC)
Fixed dose combination of Tenofovir 300 mg/Emtricitabine 200 mg or Tenofovir 300 mg/Lamivudine 300 mg plus Ritonavir Boosted Atazanavir 300/100mg given once a day

Locations

Country	Name	City	State
Argentina	Fundacion Huesped	Buenos Aires
Argentina	Dra Luna Norma	Cordoba

Sponsors (2)

Lead Sponsor	Collaborator
Pedro Cahn	Merck Sharp & Dohme Corp.

Country where clinical trial is conducted

Argentina, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Number and type of resistance mutations in case of virologic failure		Through 48 weeks
Primary	Proportion of subjects with plasma HIV-1 RNA below the limit of detection (<50 copies/mL)in an intention to treat (exposed) analysis.		48 weeks
Primary	Proportion of subjects with SAEs and proportion with AEs leading to discontinuation.		Through week 48
Secondary	Change from baseline on viral load		24 and 48 weeks
Secondary	Change from baseline in lipid profile and renal function		Through 48 weeks
Secondary	Change from baseline in inflammation markers		24 and 48 weeks