The German Institute for Quality and Efficiency in Health Care (IQWiG) has released its findings with regard to added benefit on two oncology treatments, coming to different conclusions.
In its review of US biotech major Celgene’s (Nasdaq: CELG) Imnovid/Pomalyst (pomalidomide), the health care watchdog concluded that no such added benefit could be derived, because the dossier contained no suitable data.
Imnovid has been approved since 2013 for the treatment of multiple myeloma that has returned and is difficult to treat. The drug is an option for adults who have received two or more prior treatment regimens, including treatment with the drugs lenalidomide and bortezomib, and in whom the last treatment had no sufficient effect. Pomalidomide is used in combination with the drug dexamethasone.
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