In July 2024, the Committee for Medicinal Products for Human Use of the European Medicines Agency adopted a positive opinion, recommending the granting of a marketing authorization for the medicinal product
Anzupgo, intended for the treatment of chronic hand eczema.[1][6] The applicant for this medicinal product is LEO Pharma A/S.[1] Anzupgo was approved for medical use in the European Union in September 2024.[1]
References
^ abcd"Anzupgo EPAR". European Medicines Agency. 25 July 2024. Retrieved 25 July 2024. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
^"Anzupgo PI". Union Register of medicinal products. 23 September 2024. Retrieved 27 September 2024.