Data from EMA (European Medicines Agency) - Curated by EPG Health - Last updated 09 August 2018

Indication(s)

Lenvima is indicated for the treatment of adult patients with progressive, locally advanced or metastatic, differentiated (papillary/ follicular/ Hürthle cell) thyroid carcinoma (DTC), refractory to radioactive iodine (RAI).

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Category Value
Agency product number EMEA/H/C/003727
Orphan designation Yes
Date First Approved 28-05-2015
Type Medicinal product subject to restricted medical prescription
Marketing authorisation holder Eisai Europe Ltd
Warnings This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions