Cases / 2022-01-01-D-780
discontinued2022-01-01D series

Diroximelfumarat

Schubförmig remittierende Multiple Sklerose

Open official case page ↗
Brand
Vumerity
Manufacturer
Biogen GmbH

G-BA action

discontinuation

2023-07-06

Arzneimittel-Richtlinie/Anlage XII: Diroximelfumarat (Schubförmig remittierende Multiple Sklerose) – Einstellung eines Verfahrens zur Nutzenbewertung

Evidence-checked summary

The G-BA issued a discontinuation on 2023-07-06. The official page states that it took effect as follows: 06.07.2023. The page lists Arzneimittel-Richtlinie, Anlage XII: Nutzenbewertung nach § 35a SGB V as the normative target.

This is the latest validated public action attached to this case. It is separate from the IQWiG assessment result.

Official case record

What happened, in source order

No inferred stages

Consultation record

Oral hearing and Wortprotokoll

1 hearing

2022-05-09

64 parsed turns

Oral hearing: Diroximelfumarat (Schubförmig remittierende Multiple Sklerose)

Official Wortprotokoll · 12 pages

IQWiG comparison

Assessment record versus G-BA action

1 reference

IQWiG assessment findings and the later G-BA action are separate records. Open both to compare them.

A21-172

matched

Diroximel fumarate (relapsing remitting multiple sclerosis) - Benefit assessment according to §35a Social Code Book V

Official assessment PDF · 42 pages

G-BA decisions

Distinct actions and documents

2 decision

2022-06-16

suspension

Arzneimittel-Richtlinie/Anlage XII: Diroximelfumarat (Schubförmig remittierende Multiple Sklerose) – Aussetzung des Verfahrens der Nutzenbewertung

The G-BA issued a suspension on 2022-06-16. The official page states that it took effect as follows: mit Beschlussdatum. The page lists Arzneimittel-Richtlinie, Anlage XII: Nutzenbewertung nach § 35a SGB V as the normative target.

2 official documents · 3 cited claims

2023-07-06

discontinuation

Arzneimittel-Richtlinie/Anlage XII: Diroximelfumarat (Schubförmig remittierende Multiple Sklerose) – Einstellung eines Verfahrens zur Nutzenbewertung

The G-BA issued a discontinuation on 2023-07-06. The official page states that it took effect as follows: 06.07.2023. The page lists Arzneimittel-Richtlinie, Anlage XII: Nutzenbewertung nach § 35a SGB V as the normative target.

2 official documents · 3 cited claims

Official sources

Case document package

8 source
Generic graph relations · 5