Physician Survey to Reassess Effectiveness of Strattera Risk Minimisation Activities

23/08/2013
22/02/2024
EU PAS number:
EUPAS4577
Study
Finalised
Study identification

EU PAS number

EUPAS4577

Study ID

8929

Official title and acronym

Physician Survey to Reassess Effectiveness of Strattera Risk Minimisation Activities

DARWIN EU® study

No

Study countries

Denmark
Netherlands
Sweden
United Kingdom

Study description

This is a survey to re-assess the effectiveness of the atomoxetine risk minimisation activities among physicians who prescribe Strattera and/or monitor patients being treated with Strattera.

Study status

Finalised
Research institutions and networks

Institutions

GfK Health
First published:
01/02/2024
Institution

Contact details

Nicole Kellier

Primary lead investigator

Study timelines

Date when funding contract was signed

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

Eli Lilly and Company
Regulatory

Was the study required by a regulatory body?

No