Expired Study
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Los Angeles, California 90036


Subjects with HIV who have viral suppression on current regimen but also have side effects/intolerance will change their current regimen to a combination of Raltegravir and Atazanavir and be monitored for viral and immunological response and quality of life.

Study summary:

Subjects with intolerance to current regimen will receive Raltegravir 400 mg twice daily and Atazanavir 400 mg daily will be monitored for viralogical and immunological outcomes, changes in lipids, renal and hepatic safety and quality of life.


Inclusion Criteria - History of no PI resistance or antiretroviral failure while receiving a PI. - On a current antiviral regimen with plasma HIV viral load (VL) < 400 copies/ml for 4 months or longer. - Intolerance to or toxicity with current or alternative regimen(s) with side effects including but not limited to gastrointestinal, neurological, metabolic, or dysmorphic symptoms and/or dyslipidemia. - Continuously using the same regimen for 3 months prior to Screening. - Women of childbearing potential must be willing to use effective method(s) of contraception throughout their study participation and for 30 days following the end of the study (see Section 1.10). -Women who are postmenopausal for at least 2 years, women with total hysterectomy and women with tubal ligation are considered of non-childbearing potential. - Willing to adhere to the prohibitions and restrictions specified in this protocol. Exclusion Criteria: - Use of any drug contraindicated in the current US package insert for Atazanavir or in the investigators brochure for Raltegravir, including PPI inhibitors. - Use of any investigational drug up to 4 weeks prior to screening. - Prior or current therapy with Raltegravir. - Allergy to Raltegravir or Atazanavir - History of medication non-compliance significant to the study regimen as deemed significant by the investigator. - Known achlorhydria that would inhibit the absorption of Atazanavir - Concurrent active chronic Hepatitis B requiring therapy with 3TC, FTC or Tenofovir (entecavir permitted). - AST or ALT >5 times ULN - Calculated CrCl < 30 ml/min. - Female subject who is pregnant or breastfeeding. - General medical condition that may interfere with the assessments and completion of the trial.



Primary Contact:

Principal Investigator
Peter J Ruane, MB
Peter J Ruane MD Inc

Peter J Ruane, MB
Phone: 3239541072
Email: pjruane@lightsourcemedical.com

Backup Contact:

Email: balas@lightsourcemedical.com
Brian Alas
Phone: 3239541072

Location Contact:

Los Angeles, California 90036
United States

There is no listed contact information for this specific location.

Site Status: Recruiting

Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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