WHO ICTRP trial

An Observational follow-up study to Protocol 018

EUCTR2013-001526-26-IT · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2013-001526-26-IT
Public title An Observational follow-up study to Protocol 018
Scientific title An Observational Follow-Up Study for: A Phase III Randomized, Placebo-Controlled Clinical Trial to Assess the Safety and Efficacy of Odanacatib (MK-0822) to Reduce the Risk of Fracture in Osteoporotic Postmenopausal Women Treated With Vitamin D and Calcium (Protocol 018) - An Observational follow-up…
Primary sponsor Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.
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): no Therapeutic confirmatory - (Phase III): yes Therapeutic use (Phase IV): no
Countries Serbia;United States;Philippines;Hong Kong;Estonia;Taiwan;Spain;Ukraine;Lebanon;Russian Federation;Chile;Colombia;Switzerland;Italy;India;France;Denmark;Peru;Australia;South Africa;Latvia;China;Korea…
Conditions Osteoporosis MedDRA version: 16.0 Level: PT Classification code 10031282 Term: Osteoporosis System Organ Class: 10028395 - Musculoskeletal and connective tissue disorders ;Therapeutic area: Diseases [C] - Musculoskeletal Diseases [C05]
Interventions Product Code: MK-0822 Pharmaceutical Form: Tablet CAS Number: 603139-19-1 Current Sponsor code: MK-0822 Other descriptive name: Odanacatib Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 0-
Registration date Sep 8, 2013
Target size 6000
Secondary IDs 083
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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