PRJ2203: Dolutegravir Post Authorization Safety Study (PASS)

Completed

• Conditions: Infection, Human Immunodeficiency Virus I
• Interventions: Drug: DTG based ARV regimen with ABC; Drug: RAL or EGV based regimens without ABC; Drug: Any other DTG based ARV regimen as monotherapy; Drug: DTG based ARV regimen without ABC; Drug: RAL or EGV based ARV regimens with ABC

• Registration Number: NCT03327740
• Lead Sponsor: ViiV Healthcare

Brief Summary

Dolutegravir (DTG) is recommended for both treatment-naïve and treatment-experienced, HIV infected adults and paediatric subjects aged 12 years and older and weighing at least 40 kg. One case of suspected DTG hypersensitivity (HSR) reaction from among over 1500 subjects exposed to the drug at the time of submission in 4Q2012, has been identified; this subject experienced a diffuse maculopapular rash with fever and elevated liver enzymes. Isolated rash was uncommon in the DTG programme with less than 1% of clinical trial subjects experiencing treatment related rash. The pharmacovigilance strategy for DTG and DTG-containing products is to implement a post-marketing risk management program to further quantify the risk of HSR and compare it to that of other integrase inhibitors, and to possibly determine associated risk factors. In addition, the post-authorization safety study will monitor and compare hepatotoxicity and severe skin rash following initiation of DTG or other integrase inhibitor (raltegravir (RAL) or elvitegravir (EGV) based antiretroviral regimens (ARV). Further to be able to distinguish the above symptoms and reactions caused by DTG or the other integrase inhibitor regimen from that of abacavir (ABC), known to cause hypersensitivity reaction, the integrase inhibitor groups will be compared in combinations with and without ABC. This five year-long safety study will be conducted through collaboration with EuroSIDA, a well established prospective observational cohort study of more than 18,200 subjects followed in 107 hospitals in 31 European countries, plus Israel and Argentina. This is a five year-long non-interventional prospective cohort study nested within the EuroSIDA study. The study population will include HIV positive subjects over the age of 16 years from EuroSIDA clinical sites, who are new users of DTG or other integrase inhibitors with and without ABC. Following initiation of DTG with ABC based antiretroviral regimen or DTG without ABC or regimens containing other integrase inhibitors (RAL, EGV) with or without ABC or any other DTG based ARV regimen as monotherapy or two-drug regimens, the study will aim to a) Monitor and compare hypersensitivity reaction, b) Monitor and compare hepatotoxicity, and c) Monitor and compare severe skin rash among all subjects discontinuing DTG or other integrase inhibitor regimens for any reason.

Detailed Description

Not available

Study Timeline

• Study Start: 2014-09-30
• Study First Submitted: 2017-10-27
• Study First Submitted QC: 2017-10-27
• Study First Posted: 2017-10-31
• Primary Completion: 2019-12-31
• Study Completion: 2019-12-31
• Status Verified: 2020-02
• Last Update Submitted: 2020-02-05
• Last Update Posted: 2020-02-06

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 1

Inclusion Criteria

• New users of DTG or users of other integrase inhibitor regimens (RAL and EGV)

Exclusion Criteria

• None

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Subjects on DTG based ARV with ABC	DTG based ARV regimen with ABC	These are subjects who begin a DTG based ARV regimen that includes ABC
Subjects on other integrase inhibitor based regimen but no ABC	RAL or EGV based regimens without ABC	These are subjects that start non-ABC containing RAL or EGV based regimens
Subjects that start any other DTG based ARV regimen	Any other DTG based ARV regimen as monotherapy	These are subjects who begin any other DTG based ARV regimen that will include DTG as monotherapy or two-drug regimens
Subjects that start DTG based ARV regimen but without ABC	DTG based ARV regimen without ABC	These are subjects who begin a DTG-based ARV regimen that does not contain ABC
Subjects on other integrase inhibitor based regimen with ABC	RAL or EGV based ARV regimens with ABC	These are subjects who begin other integrase inhibitor based regimens (RAL and EGV) that contains ABC

Primary Outcome Measures

Name	Time	Method
Number of subjects with hepatic dysfunction	Up to 5 years	Hepatic dysfunction will be indicated by liver chemistry tests
Number of subjects with occurrence of hypersensitivity reactions (HSR), of any grade	Up to 5 years	Hypersensitivity reactions including fever, rash, gastrointestinal symptoms, constitutional symptoms, respiratory symptoms and eosinophilia will be summarized.