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

21/07/2016
02/07/2024
EU PAS number:
EUPAS14290
Study
Finalised
Study summary
No information provided.
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

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