Double Protease Inhibitor to Darunavir Switch Study

St Stephens Aids Trust

Status and phase: Completed; Phase 4

Conditions: HIV Infections

Treatments: Drug: Darunavir ritonavir

Study type: Interventional

Funder types: Other

Identifiers

NCT00531557

SSAT022

Details and patient eligibility

About

The purpose of the study is to study the effects of switching from an antiretroviral combination that includes two ritonavir boosted protease inhibitors to replacement of these two protease inhibitors with a new protease inhibitor called Darunavir (also boosted with ritonavir).

The study will investigate the effect of the switch on viral load (the levels of the HIV virus in the blood), on immunological parameters (CD4 count) and on other safety parameters and also on quality of life.

In a subgroup of patients the impact of the switch on the body's response to the hormone insulin will also be measured (Euglycaemic clamp sub group)

Full description

HIV-RNA and CD4+ cell count to monitor virological and immunological response on switching to DRV/r.

Routine safety bloods to include haematology and biochemistry (including U&E, fasted glucose and insulin, liver function test, fasting cholesterol and triglycerides and serum lactate measurements).

Quality of life EuroQOL questionnaires at baseline, and throughout the study to evaluate quality of life in the continued treatment/ treatment switch arms.

A sub group of 10 patients will undergo two euglycaemic clamp procedures in order to determine the extent of glucose disposal. The first clamp will be performed prior to the switching from a double boosted PI therapy to DRV/r and the second one following administration of DRV/r for 4 weeks.

Enrollment: 12 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. HIV-1 infected as documented by a licensed HIV-1 antibody ELISA test
2. At least 18 years of age
3. Currently on an antiretroviral regimen including a ritonavir boosted double protease inhibitor
4. The subject is virologically suppressed with a viral load < 50 copies/mL for three months or longer
5. The subject has a CD4+ count above 100 cells/mL
6. ≤ Three DRV associated mutations on previous genotypic resistance test -or if no resistance test available, likely to have ≤ four protease inhibitor mutations based on their clinical history
7. If the subject is a woman of child bearing potential, she must agree to use a barrier method of contraception
8. The ability to understand and sign a written informed consent form, prior to participation in any screening procedures and must be willing to comply with all study requirements

Exclusion criteria

1. Pregnant or lactating women

2. Individuals with prior darunavir exposure

3. Previous allergic or hypersensitivity reaction to darunavir

4. Clinical or laboratory evidence of significantly decreased hepatic function or decompensation, irrespective of liver enzyme levels (liver insufficiency)

5. Subjects diagnosed with acute viral hepatitis at screening

6. Subjects with a grade 3 or 4 laboratory abnormality as defined by DAIDS grading table (see appendix 3: DAIDS AE grading Table), with the following exceptions unless clinical assessment foresees an immediate health risk to the subject:

   • Subjects with pre-existing diabetes or with asymptomatic glucose grade 3 or 4 elevations
   • Subjects with asymptomatic triglyceride or cholesterol elevations of grade 3 or 4.

7. Presence of any currently active AIDS defining illness (Category C conditions according to the CDC Classification System for HIV Infection 1993) with the following exceptions: Stable cutaneous Kaposi's Sarcoma (i.e., no internal organ involvement other than oral lesions) that is unlikely to require any form of systemic therapy during the study; Wasting syndrome due to HIV infection.

   Note: An AIDS defining illness that is not clinically stabilized for at least 30 days will be considered as currently active.

8. Active drug abuse, including alcohol or recreational drugs, which, in the opinion of the investigator, is expected to interfere with the subject's ability to adhere to the study procedures and treatment regimen. Subjects on a methadone program will be accepted if deemed appropriate by the investigator.

Trial design

12 participants in 1 patient group

1

Other group

Description:

Darunavir 600mg BID with ritonavir 100mg BID administered orally.

Treatment:

Drug: Darunavir ritonavir