Cases / 2020-03-15-D-514
completed2020-03-15D series

Brolucizumab

Neovaskuläre altersabhängige Makuladegeneration

Open official case page ↗
Brand
Beovu®
Manufacturer
Novartis Pharma GmbH

G-BA action

final resolution

2020-09-03

Arzneimittel-​​​Richtlinie/Anlage XII: Brolucizumab (Neovaskuläre altersabhängige Makuladegeneration)

Evidence-checked summary

The G-BA found no proven added benefit for Erwachsene mit neovaskulärer (feuchter) altersabhängiger Makuladegeneration. The appropriate comparator was - Ranibizumab oder Aflibercept. The G-BA issued a final resolution on 2020-09-03. The official page states that it took effect as follows: aufgehoben. 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.

Final benefit result

G-BA result by patient group

Open decision 4449 →

Patient group

Erwachsene mit neovaskulärer (feuchter) altersabhängiger Makuladegeneration

Added benefit not proven

Comparator
- Ranibizumab oder Aflibercept

Open official result PDF ↗

Official case record

What happened, in source order

No inferred stages

Consultation record

Oral hearing and Wortprotokoll

1 hearing

2020-07-27

36 parsed turns

Oral hearing: Brolucizumab (Neovaskuläre altersabhängige Makuladegeneration)

Official Wortprotokoll · 8 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.

A20-23

matched

Brolucizumab (neovascular age-related macular degeneration) - Benefit assessment according to §35a Social Code Book V

Official assessment PDF · 32 pages

G-BA decisions

Distinct actions and documents

1 decision

2020-09-03

final resolution

Arzneimittel-​​​Richtlinie/Anlage XII: Brolucizumab (Neovaskuläre altersabhängige Makuladegeneration)

The G-BA found no proven added benefit for Erwachsene mit neovaskulärer (feuchter) altersabhängiger Makuladegeneration. The appropriate comparator was - Ranibizumab oder Aflibercept. The G-BA issued a final resolution on 2020-09-03. The official page states that it took effect as follows: aufgehoben. The page lists Arzneimittel-Richtlinie, Anlage XII: Nutzenbewertung nach § 35a SGB V as the normative target.

3 official documents · 4 cited claims

Official sources

Case document package

7 source
Generic graph relations · 4