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NMPA (China) approves Gamifant for primary haemophagocytic lymphohistiocytosis- SOBI .

Read time: 1 mins
Published: 19th Mar 2022

Sobi announced that the National Medical Products Administration of China (NMPA) has approved Gamifant (emapalumab) for use in China. The indication is for treatment of adult and paediatric (newborn and older) patients with primary haemophagocytic lymphohistiocytosis (HLH) with refractory, recurrent or progressive disease or intolerance to conventional HLH therapy.

 

The approval followed the recommendation announced in February 2022. Primary HLH is an ultra-rare, life-threatening, hyperinflammatory disorder, characterised by uncontrolled activation of the immune system. Morbidity and mortality are high due to lack of detection and non-specific symptoms, but if diagnosed early and appropriately treated, the inflammation and damage can be reduced. Gamifant represents a new treatment option for patients with progressive disease through a targeted mode of action.

Condition: Primary Hemophagocytic Lymphohistiocytosis
Type: drug
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