Switch to Maraviroc + Integrase Inhibitor

HIV Clinical Trial

Official title:

Switch to Maraviroc and Integrase Strand Transfer Inhibitor Combination Therapy (a Triple Class-Sparing Regimen) for the Treatment of HIV-1-Infected Patients on Suppressive Antiretroviral Regimens

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01896921
• Other study ID #: HP-00056162
• Status: Completed
• Phase: Phase 3
• Start date: September 2013
• Est. completion date: December 2018

Study information

• Verified date: October 2021
• Source: University of Maryland, Baltimore
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This clinical study proposes to evaluate the combination of maraviroc with an integrase strand transfer inhibitor (either raltegravir or dolutegravir) in antiretroviral-experienced patients to document the efficacy, safety, and tolerability of this combination in order to provide clinicians with a treatment regimen that minimizes the risk of metabolic complications by avoidance of NRTI/NNRTIs and PIs. The development of an alternative ART regimen which lessens the risk of metabolic complications could improve long-term adherence and reduce the risk of certain co-morbidities associated with long-term ART use. If this new combination is found to be as efficacious as the standard regimen with enhanced tolerability and improved metabolic effects, there is great potential for altering the current practice of HIV medicine.

Description:

Description of the study design:

The study will enroll 30 HIV-infected patients on a stable ART regimen with a suppressed HIV RNA < 50 copies/ml for at least one year. Patients will be switched to the experimental regimen (maraviroc 300 mg twice a day plus either raltegravir 400 mg twice a day or dolutegravir 50 mg once a-day) and followed for 96 weeks. The decision to use raltegravir or dolutegravir will be left to investigator/subject preference, as the two integrate inhibitors are largely interchangeable aside from twice daily (raltegravir) vs. daily (dolutegravir) dosing.

Primary endpoint:

• The primary endpoint is the proportion of patients virologically suppressed (HIV RNA < 50 copies/ml) at 48 weeks.

Definitions:

• Virologic suppression is an HIV RNA < 50 copies/ml.

• Virologic failure is an HIV RNA ≥ 50 copies/ml confirmed on 2 separate occasions, separated by > 1 week after viral suppression.

Secondary endpoints:

• The percent change in total cholesterol, LDL, and HDL at 48 and 96 weeks.

• The number of adverse events.

• The proportion of patients who are virologically suppressed (HIV RNA < 50 copies/ml) at 96 weeks.

Exploratory endpoints:

• Telomerase activity and telomere length measured at baseline and 24, 48, and 96 weeks.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 7
• Est. completion date: December 2018
• Est. primary completion date: December 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• HIV-1 infection

• Age between 18 and 75 years

• CD4 count nadir = 250 cells/mm3

• HIV RNA = 50 copies/ml for = 12 months while taking any ART regimen

o One virologic blip = 400 copies/ml permissible within the 12 months

• CCR5 tropic virus as defined by:

• trofile/tropism testing if available, OR

• DNA trofile if no trofile/tropism test available and CD4 nadir 250-499 cells/mm3, OR

• CD4 nadir = 500 cells/mm3

Exclusion Criteria:

• Age < 18 or > 75 years

• CD4 count nadir < 250 cells/mm3

• Dual/mixed or X4 tropic virus if tested prior to viral suppression or if performed by DNA trofile testing at any time

• Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) >2.5 times the upper limits of normal

• Women who:

• are currently pregnant or breastfeeding

• are of child-bearing age and do not agree to remain abstinent or use (or have their partner use) an acceptable method of birth control throughout the study. Acceptable method of birth control is defined as intrauterine device (IUD), diaphragm with spermicide, contraceptive sponge, condom, vasectomy.

• History of any malignancy except non-melanoma skin cancer

• Concomitant use of drugs known to impact or be impacted in terms of pharmacokinetics or drug-drug interactions with either raltegravir or maraviroc. This includes:

• Inducers of UGT1A1 (such as rifampin, phenytoin, phenobarbital rifabutin, St. John's wort)

• CYP3A inhibitors (such as ketoconazole, itraconazole, clarithromycin, nefazodone, and telithromycin)

• CYP3A inducers (such as rifampin, carbamazepine, phenobarbital and phenytoin)

• Subject requires or is anticipated to require any of the prohibited medications noted in the protocol

• Enrollment in an experimental protocol having received investigational agents (antiretroviral or non-antiretroviral) within 30 days of study enrollment

• Chronic active hepatitis B infection as defined by presence of HBsAg

• Subject has a history or current evidence of any condition, therapy, laboratory abnormality or other circumstance that might interfere with the patient's participation for the full duration of the study, such that it is not in the best interest of the patient to participate.

• Subject is unlikely to adhere to the study procedures, keep appointments, or is planning to relocate during the study.

Related Conditions & MeSH terms

• HIV

Intervention

Drug:
• Switch to Maraviroc + Raltegravir or Dolutegravir
Change HIV-infected patients on stable, suppressed ART regimens for at least 1 year to experimental regimen of Maraviroc + Raltegravir or Dolutegravir for 48 weeks

Locations

Country	Name	City	State
United States	University of Maryland, Institute of Human Virology	Baltimore	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
University of Maryland, Baltimore

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Patients Virologically Suppressed (HIV RNA <50 Copies/ml) at 48 Weeks.	Number of patients virologically suppressed (HIV RNA <50 copies/ml) at 48 weeks.	48 weeks
Secondary	Number of Participants With Adverse Events	Number of participants with adverse events	96 weeks
Secondary	Number of Patients Who Are Virologically Suppressed (HIV RNA < 50 Copies/ml)	Number of patients who are virologically suppressed (HIV RNA < 50 copies/ml)	96 weeks