Study identification

EU PAS number

EUPAS14290

Study ID

42114

Official title and acronym

Rates of Suspected Hypersensitivity Reaction to Abacavir and Associated Rates of HLA-B*5701 Testing (206206)

DARWIN EU® study

No

Study countries

United States

Study description

Rates of suspected hypersensitivity reaction (HSR) associated with the use of abacavir (ABC) and associated rates of HLA-B*5701 testing in HIV positive patients living in the U.S. who have been exposed to ABC as part of an antiretroviral therapy (ART) regimen will be evaluated utilizing prospectively-collected electronic medical record (EMR) data obtained from the Observational Pharmaco-Epidemiology Research & Analysis (OPERA®) Observational Database

Study status

Finalised
Research institutions and networks

Institutions

ViiV Healthcare
First published:
01/02/2024
Institution

Contact details

GSK Clinical Disclosure Advisor GSK Clinical Disclosure Advisor Pharma.CDR@gsk.com

Study contact

GSK Clinical Disclosure Advisor GSK Clinical Disclosure Advisor

Primary lead investigator
Study timelines

Date when funding contract was signed

Planned:
Actual:

Study start date

Planned:
Actual:

Data analysis start date

Planned:
Actual:

Date of final study report

Planned:
Actual:
Sources of funding
Pharmaceutical company and other private sector 

More details on funding

ViiV Healthcare
Regulatory

Was the study required by a regulatory body?

No

Is the study required by a Risk Management Plan (RMP)?

Not applicable