Elvitegravir/Cobicistat/Tenofovir DF/Emtricitabine With Darunavir Treatment Simplification Strategy

HIV Infection Clinical Trial

— QuaDar  

Official title:

Elvitegravir/Cobicistat/Tenofovir DF/Emtricitabine With Darunavir in Treatment-experienced Patients: Quality Control Monitoring of a Treatment Simplification Strategy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02199613
• Other study ID #: H14-00490
• Secondary ID: H14-00490
• Status: Completed
• Phase: Phase 4
• First received: July 22, 2014
• Last updated: November 1, 2017
• Start date: October 2014
• Est. completion date: February 14, 2017

Study information

• Verified date: November 2017
• Source: University of British Columbia
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study aims to assess the safety and efficacy of darunavir 800mg plus the co-formulated elvitegravir/cobicistat/tenofovir disoproxil fumarate (DF)/emtricitabine (Stribild) tablet as a simplification strategy for the treatment of HIV infection in HIV-infected subjects who have had previous antiretroviral treatment experience with multiple-drug regimens.

We hypothesize that elvitegravir/cobicistat/tenofovir DF/emtricitabine with darunavir will offer a safe and efficacious treatment simplification strategy for HIV positive patients currently receiving multiple-drug regimens to control their HIV infection.

Description:

Eligible, consenting subjects will be assessed at baseline and weeks 2, 12, 24, 36, and 48. Study medications will be dispensed at all visits except week 2, and all participants will commence taking open-label darunavir 800mg in conjunction with the co-formulated tenofovir DF/emtricitabine/cobicistat/elvitegravir (Stribild) tablet, both taken together once daily with food, following study procedures at baseline.

Assessments at the study visits will include:

1. Complete physical exam including height and weight at baseline; symptom-directed physical exam and weight at other visits

2. Adverse clinical events including serious adverse events (hospitalizations etc.) and medication changes at every visit.

3. HIV RNA every 4 weeks.

4. CD4 and CD8 absolute counts and % at all visits except week 2.

5. Platelet count, aspartate amino transferase (AST), creatinine, estimated glomerular filtration rate (eGFR), phosphorus, urinalysis, and urine albumin to creatinine ratio (UACR) at each visit.

6. Fasting lipids (total, HDL, and LDL cholesterol and triglycerides), apolipoprotein B, high-sensitivity C- reactive protein (hsCRP) at baseline, week 24, and week 48.

7. Pregnancy test for women of child-bearing potential (as defined above) at every visit except week 2. In addition, pregnancy tests will be performed monthly for women of child-bearing potential; between study visits these may be done at home.

8. A plasma sample (3 mL) will be collected and stored once at baseline for all subjects, and used for measurement of darunavir trough (pre-dose) concentration in subjects receiving darunavir in their pre-study regimen.

9. All subjects will take their study medication under observation in the clinic on Day 14, and plasma samples (3mL) for pharmacokinetic testing will be drawn immediately pre-dose and at 1, 2, 3, 4, 5, 6, and 8 hours post-dose. Subjects will return the following day before taking their Day 15 dose for a 24-hour post-dose sample.

10. Peripheral blood mononuclear cells (PBMCs) will be collected and stored at baseline for possible future study-related testing.

11. The following questionnaires will be completed by participants prior to other study procedures at baseline and at weeks 24 and 48: MOS-HIV quality of life questionnaire; HIVTSQ; ACTG treatment adherence questionnaire; and the medication adherence self-report inventory (MASRI).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: February 14, 2017
• Est. primary completion date: February 14, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 19 Years and older

Eligibility

Inclusion Criteria:

• HIV positive adults > or = 19 years of age

• receiving stable therapy including one or two nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs), in conjunction with a once-daily protease inhibitor (PI) (atazanavir, lopinavir or darunavir) and twice daily raltegravir or once daily dolutegravir

• Virologic suppression for >6 months, defined as plasma viral load (VL) consistently < 200 copies/mL with no evidence of prior virologic rebound (VL > 1000 copies/mL) on the NRTI/PI/Raltegravir regimen, AND VL < 50 copies/mL at time of study screening

• Estimated glomerular filtration rate (eGFR) > o r= 70mL/min at screening

Exclusion Criteria:

• Prior documented viral rebound > 1000 copies/mL on any raltegravir-containing regimen

• Evidence of resistance mutations compromising raltegravir or elvitegravir activity on prior genotypes.

• Evidence of clinically significant resistance to tenofovir on any previous genotype tests: K65R mutation, or 3 or more thymidine-analogue associated mutations (TAMS) compromising tenofovir activity

• Evidence of resistance mutations significantly compromising darunavir activity on any previous genotypic tests

• Current use of any nonnucleoside reverse transcriptase inhibitor (NNRTI)

• Pregnancy or breast-feeding

• Contraindications to tenofovir/FTC, elvitegravir, or cobicistat (e.g. previous significant toxicity, intolerance or drug interactions

Related Conditions & MeSH terms

• HIV Infection
• HIV Infections

Intervention

Drug:
• Treatment simplification
Eligible, consenting subjects will start open-label darunavir 800mg plus the co-formulated tenofovir DF/FTC/cobicistat/elvitegravir (Stribild) tablet once daily with food, following the study procedures at the baseline visit. They will be assessed at weeks 2, 12, 24, 36, and 48 after starting the new regimen.

Locations

Country	Name	City	State
Canada	St. Paul's Hospital Immunodeficiency Clinic	Vancouver	British Columbia

Sponsors (2)

Lead Sponsor	Collaborator
University of British Columbia	Gilead Sciences

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Plasma HIV RNA	Proportion of individuals with plasma HIV RNA <200copies/mL at 12 weeks following regimen switch	12 weeks
Secondary	plasma HIV RNA	Proportion of individuals with plasma HIV RNA < 50 copies/mL at weeks 12, 24 and 48 post switch	weeks 12, 24 and 48
Secondary	plasma HIV RNA	Proportion of individuals with plasma HIV RNA < 200 copies/mL at week 24 and 48 post switch	week 24 and 48
Secondary	CD4 cell count, CD4% and CD4/CD8 ratio	Change in CD4 cell count, CD4% and CD4/CD8 ratio from study baseline to 12, 24 and 48 weeks after switch.	12, 24 and 48 weeks
Secondary	serum creatinine and estimated glomerular filtration rate (eGFR)	Change in serum creatinine and eGFR from baseline to 12, 24 weeks and 48 weeks.	12, 24, and 48 weeks
Secondary	Adverse event discontinuations	Proportion of adverse events experienced necessitating switch to original regimen	48 weeks
Secondary	fasting lipid parameters (total cholesterol, LDL, HDL, triglycerides, and apolipoprotein B [apoB]), AST to platelet ratio index (APRI) score, and high-sensitivity C-reactive protein (hsCRP)	Changes in fasting lipid parameters (total cholesterol, LDL, HDL, triglycerides, and apolipoprotein B [apoB]), AST to platelet ratio index (APRI) score, and high-sensitivity C-reactive protein (hsCRP) between baseline and 24 and 48 weeks.	24 and 48 weeks
Secondary	Darunavir plasma concentration	Change in darunavir trough concentration from baseline to week 2 for individuals receiving darunavir at baseline	week 2
Secondary	HIV Treatment Satisfaction Questionnaire (HIVTSQ) scores and quality of life indicators (MOS-HIV scores)	Changes in HIV Treatment Satisfaction Questionnaire (HIVTSQ) scores and quality of life indicators (MOS-HIV scores) between baseline and weeks 24 and 48 following switch.	weeks 24 and 48
Secondary	Adherence	Changes in antiretroviral adherence from baseline to 24 and 48 weeks. Adherence will be assessed using two measures: the ACTG treatment adherence questionnaire and the Medication adherence self-report inventory (MASRI).	24 and 48 weeks
Secondary	Elvitegravir plasma concentrations	Elvitegravir concentrations will be measured at day 14	Day 14
Secondary	Adverse events	Adverse events necessitating a resumption of the previous antiretroviral regimen, and all serious adverse events will be recorded.	48 weeks