Trial Profile
A multicenter, prospective, randomized, 2-way crossover, open-label study in postmenopausal women with osteoporosis examining subject satisfaction and compliance when risedronate sodium [risedronic acid](Actonel) is administered 35mg once a week or 5mg once daily.
Status:
Completed
Phase of Trial:
Phase IV
Latest Information Update: 16 Jul 2009
Price :
$35
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At a glance
- Drugs Risedronic acid (Primary)
- Indications Postmenopausal osteoporosis
- Focus Therapeutic Use
- Sponsors Sanofi
- 07 Jun 2007 New trial record.