Clinical Trial Results:
A 24-week, international, multi centre, randomised, open label, parallel group, phase IV clinical trial investigating changes in bone formation markers in postmenopausal women with primary osteoporosis treated with either PTH(1-84) or strontium ranelate
Summary
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EudraCT number |
2006-006065-16 |
Trial protocol |
AT ES |
Global completion date |
26 Jan 2009
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Paediatric regulatory details
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Is the trial part of an agreed EMA paediatric investigation plan? |
No
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Is the trial in scope of article 45 of Regulation (EC) No 1901/2006? |
No
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Is the trial in scope of article 46 of Regulation (EC) No 1901/2006? |
No
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Results information
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Results version number |
v1(current) |
This version publication date |
24 Jun 2016
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First version publication date |
24 Jun 2016
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Other versions |
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Summary report(s) |
Results Disclosure |
Note: The legislation allows summary attachments to be posted instead of the full dataset for this trial. Refer to Commission Guideline 2012/C 302/03
for further information.