Clinical Trial Results:
Randomized, controlled, double-blind multicenter safety study to evaluate the safety and immunogenicity of subcutaneous EPO HEXAL vs. ERYPO® in the treatment of anemia associated with chronic renal insufficiency in predialysis patients
Summary
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EudraCT number |
2007-001906-26 |
Trial protocol |
DE AT SK FR BG |
Global completion date |
11 Jan 2010
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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 |
29 Dec 2016
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First version publication date |
29 Dec 2016
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Other versions |
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Summary report(s) |
INJ-17 Clinical trial Results_Sandoz |
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.