WHO ICTRP trial

SAFETY AND TOLERABILITY OF ODM-201 IN PATIENTS WITH PROSTATE CANCER: EXTENSION…

EUCTR2010-022803-24-GB · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2010-022803-24-GB
Public title SAFETY AND TOLERABILITY OF ODM-201 IN PATIENTS WITH PROSTATE CANCER: EXTENSION STUDY TO STUDY 3104001
Scientific title SAFETY AND TOLERABILITY OF ODM-201 IN PATIENTS WITH CASTRATE RESISTANT PROSTATE CANCER: OPEN, NON-RANDOMISED, UNCONTROLLED, MULTICENTRE, EXTENSION STUDY TO STUDY 3104001 - Arades-Ext Phase II
Primary sponsor Orion Corporation Orion Pharma
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries France;United States;Estonia;Czech Republic;Finland;United Kingdom
Conditions Progressive castration resistant prostate cancer (MedDRA: hormone-refractory prostate cancer) MedDRA version: 14.1 Level: LLT Classification code 10062904 Term: Hormone-refractory prostate cancer System Organ Class: 10029104 - Neoplasms…
Interventions Product Name: ODM-201 Product Code: ODM-201 Pharmaceutical Form: Capsule INN or Proposed INN: . Current Sponsor code: ODM-201 Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 100-
Registration date Nov 15, 2010
Target size 130
Secondary IDs 3104002
Registry page clinicaltrialsregister.eu

At a glance

  • Yes Results available

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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