Takeda Secures EMA Approval for Additional Injection Option for Hereditary Angioedema Drug

MT Newswires Live

02-24

武田製藥1.30%

Takeda Pharmaceutical Co (TAK) said Monday that the European Medicines Agency has approved an additional subcutaneous administration option for hereditary angioedema drug TAKHZYRO, or lanadelumab.

The drug now comes in a 2 mL pre-filled pen for adolescent and adult patients, the company said.

Hereditary angioedema is a rare genetic disease that causes severe swelling in the body.

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