Study identification

PURI

https://redirect.ema.europa.eu/resource/42090

EU PAS number

EUPAS6186

Study ID

42090

Official title and acronym

Survey of prescriber understanding of specific risks associated with TROBALT (201426)

DARWIN EU® study

No

Study countries

Austria
Belgium
Bulgaria
France
Hong Kong
Italy
Norway
Poland
Slovenia
Spain
Switzerland
United Kingdom

Study status

Finalised
Research institutions and networks

Institutions

Contact details

GSK Clinical Disclosure Advisor GSK Clinical Disclosure Advisor

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:

Date of final study report

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

More details on funding

GlaxoSmithKline
Study protocol
Initial protocol
English (736.84 KB - PDF)View document
Updated protocol
English (765.63 KB - PDF)View document
Regulatory

Was the study required by a regulatory body?

No

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

EU RMP category 3 (required)