Efficacy and Safety of Oral Salmon Calcitonin in Patients With Knee Osteoarthritis (OA 2 Study)

Stopped early · Phase 3 · Has a placebo group

Conditions studied: Osteoarthritis

In brief

The purpose of this phase III study is to Evaluate the Efficacy and Safety of Oral Salmon Calcitonin in the Treatment of Patients with Osteoarthritis of the Knee

Key facts

Study ID

NCT00704847

Run by

Nordic Bioscience A/S

People needed

1030

Starts

2008-06-01

Expected to finish

2011-06-01

Last updated by the study team

2019-04-24

Who can join

Age: 51 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Medical history and symptoms of knee osteoarthritis

You may not qualify if…

• Any other disease or medication affecting the bone or cartilage.
• Any clinical signs or laboratory evidence diseases, which in the Investigator's opinion would preclude the participant from adhering to the Protocol or completing the trial.
• Other protocol defined inclusion/exclusion criteria may apply

Where it is running

• Achieve Clinical Research, LLC — Tuscaloosa, Alabama, United States
• Center for Healthy Aging — Sacramento, California, United States
• Northwestern Center for Clinical Research — Chicago, Illinois, United States
• Midwest Pharmaceutical Research — City of Saint Peters, Missouri, United States
• Thurston Arthritis Research Center — Chapel Hill, North Carolina, United States
• Rheumatology Clinical Research Unit — Beachwood, Ohio, United States
• Hospital Universitaire St. Luc, UCL 5390 — Brussels, Belgium
• Centre de Rhumatologie St-Louis — Sainte-Foy (Québec), Canada
• CCBR Czech — Pardubice, Czechia
• CCBR Aalborg — Aalborg, Denmark
• CCBR Ballerup — Ballerup Municipality, Denmark
• CCBR Vejle — Vejle, Denmark
• CCBR Hong Kong — Hong Kong, Hong Kong
• Centrum Osteoporozy i Chorób Kostno Stawowych, ul. Waryńskiego 6/2 — Bialystok, Poland
• CCBR Poland — Warsaw, Poland
• CCBR Romania — Bucharest, Romania
• Hospital Universitario de la Paz — Madrid, Spain
• Little Common Surgery — Bexhill-on-Sea, East Sussex, United Kingdom

Full record on ClinicalTrials.gov

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