Observational prospective study describing the global patient care and follow-up of prostate cancer patients treated with Degarelix (DUO study (Dialogue in Uro-Oncology))

20/06/2017
02/04/2024
EU PAS number:
EUPAS18906
Study
Finalised
Study summary
No information provided.
Study identification

EU PAS number

EUPAS18906

Study ID

46959

Official title and acronym

Observational prospective study describing the global patient care and follow-up of prostate cancer patients treated with Degarelix (DUO study (Dialogue in Uro-Oncology))

DARWIN EU® study

No

Study countries

France

Study description

The DUO study's main objective is to evaluate, in the real life, the prevalence of cardiovascular comorbidities among prostate cancer patients receiving Degarelix, before treatment. This study will also assess, at the initiation of therapy, the prevalence of osteoporosis, metabolic comorbidities, depression, sexual and geriatric patients suffering from prostate cancer.

Study status

Finalised
Research institutions and networks

Institutions

Multiple centres: 60 centres are involved in the study

Contact details

Pierre Mongiat-Artus

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

Ferring SAS
Regulatory

Was the study required by a regulatory body?

No

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

Not applicable