Clinical trial

Phase II/III Clinical Study of R484iv (Ibandronic Acid) for Primary Osteoporosis

NCT00447915 · Chugai Pharmaceutical, Industry · Completed

Key facts

NCT number NCT00447915
Title Phase II/III Clinical Study of R484iv (Ibandronic Acid) for Primary Osteoporosis
Official title Phase II/III Clinical Study of R484iv (Ibandronic Acid) for Primary Osteoporosis - Comparative Study With Sodium Risedronate Hydrate(RIS) With Vertebral Fracture as an Index -
Lead sponsor Chugai Pharmaceutical, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Primary Osteoporosis
Intervention type Dietary Supplement, Drug
Interventions ibandronic acid 0.5mg, RIS placebo, 1.0mg ibandronic acid, ibandronic acid placebo, 2.5mg RIS, Calcium and Vitamine D3
Enrollment 1,265
Start date Mar 1, 2007
Primary completion Aug 1, 2011
Completion Dec 1, 2011
First posted Mar 15, 2007
Last update posted Aug 2, 2012
Countries Japan

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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