IQWiG says Octapharma provided no suitable data on Nuwiq to show added benefit
The German Institute for Quality and Efficiency in Health Care (IQWiG) has examined data on independent Swiss biotech firm Octapharma's Nuwiq (simoctocog alfa), concluding that an added benefit cannot be derived from the dossier because the drug manufacturer did not submit any suitable data.
The European Commission approved Nuwiq for the treatment and prophylaxis of bleeding in all age groups with hemophilia A (congenital factor VIII [FVIII] deficiency) last year.
Studies only compared single-dose administration of the drugs
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