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Study to assess the efficacy, safety and pharmacokinetics of risedronate [risedronic acid] upon oral administration of a 35 mg delayed-release, a 50 mg delayed-release or a 35 mg immediate-release administered weekly for 13 weeks to postmenopausal women.

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Trial Profile

Study to assess the efficacy, safety and pharmacokinetics of risedronate [risedronic acid] upon oral administration of a 35 mg delayed-release, a 50 mg delayed-release or a 35 mg immediate-release administered weekly for 13 weeks to postmenopausal women.

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 10 Nov 2021

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At a glance

  • Drugs Risedronic acid (Primary)
  • Indications Postmenopausal osteoporosis
  • Focus Therapeutic Use
  • Sponsors Procter & Gamble

    • Most Recent Events

    • 12 Jan 2012 Actual patient number is 181 as reported by ClinicalTrials.gov.
    • 24 Mar 2010 Additional lead trial centre identified as reported by ClinicalTrials.gov.
    • 24 Mar 2010 Actual number of patients added to 168 as reported by ClinicalTrials.gov.

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