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Efficacy and Safety of Actonel® After Denosumab Discontinuation in Postmenopausal Osteoporosis Women

Efficacy and Safety of Actonel® After Denosumab Discontinuation in Postmenopausal Osteoporosis Women

Non Recruiting
50-80 years
Female
Phase 4
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Overview

To evaluate the effect of 1 year of risedronate treatment on the prevention of bone loss after denosumab discontinuation in denosumab-treated post-menopausal osteoporosis for a year

Eligibility

Main Inclusion Criteria:

  1. Postmenopausal women
  2. Patients diagnosed with postmenopausal osteoporosis and administered denosumab for 1 year

Main Exclusion Criteria:

  1. Any contraindication to risedronate
  2. Those evaluated as inappropriate at the discretion of the investigator

Study details
    Postmenopausal Osteoporosis

NCT05630768

Dong-A ST Co., Ltd.

20 August 2025

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