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Home » Find Clinical Trials » The efficacy and safety of a daily oral administration of S06911 (strontium ranelate 2g/vitamin D3 1000 IU fixed combination) on vitamin D deficiency in the treatment of osteoporotic postmenopausal women and men. A 12 month, prospective, open labelled, one treatment group international phase III study.

The efficacy and safety of a daily oral administration of S06911 (strontium ranelate 2g/vitamin D3 1000 IU fixed combination) on vitamin D deficiency in the treatment of osteoporotic postmenopausal women and men. A 12 month, prospective, open labelled, one treatment group international phase III study.

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Study Phase	Phase 3

Therapeutic Area	Rheumatology

Indication	Osteoporosis

Sponsor	Institut de Recherches Internationales Servier (I.R.I.S)

Active substance/ Medical device	STRONTIUM RANELATE, VITAMINE D, S006911

Active Substance Code	S006911

Protocol Code	CL3-06911-003

EudraCT Code	2009-014270-18

ISRCTN Code	ISRCTN47943635

Documents and links

Results summary	READ MORE

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