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Pharmaceuticals Directive (AM RL)
Federal Joint Committee (G-BA)
Annex XII – Benefit Assessment of Medicinal Products with New Active Ingredients According to Section 35a SGB V
Ivacaftor/Tezacaftor/Elexacaftor (Exceeding the € 50 Million Limit
Cystic Fibrosis
Combination Treatment with Ivacaftor in Patients 12 Years and Older (Homozygous for F508del Mutation))
Adobe PDF Library 15.0
Annex XII – Benefit Assessment of Medicinal Products with New Active Ingredients According to Section 35a SGB V
Ivacaftor/Tezacaftor/Elexacaftor (Exceeding the € 50 Million Limit, Cystic Fibrosis, Combination Treatment with Ivacaftor in Patients 12 Years and Older (Homozygous for F508del Mutation))
D:20210311152614
Gemeinsamer Bundesausschuss, (www.g-ba.de)
Anlage 1 zu TOP 8.1.13
Nr. XXX (S. XX XXX)
Arzneimittel-Richtlinie (AM-RL):
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