Cases / 2025-01-01-D-1143
discontinued2025-01-01D series

Bulevirtid

Neues Anwendungsgebiet: Hepatitis-Delta-Virus (HDV)-Infektion, HDV-RNA-positiv, ≥ 3 bis < 18 Jahre, ≥ 10 kg KG

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Brand
Hepcludex
Manufacturer
Gilead Sciences GmbH

G-BA action

discontinuation

2025-06-18

Arzneimittel-Richtlinie/Anlage XII: Bulevirtid (Hepatitis-Delta-Virus (HDV)-Infektion, HDV-RNA-positiv, ≥ 3 bis < 18 Jahre, ≥ 10 kg KG) – Einstellung eines Verfahrens zur Nutzenbewertung

Evidence-checked summary

The G-BA issued a discontinuation on 2025-06-18. The official page states that it took effect as follows: 18.06.2025. 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

0 hearing

The official source states that the planned oral hearing on 2025-05-05 did not take place. No Wortprotokoll exists.

IQWiG comparison

Assessment record versus G-BA action

0 reference

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

No IQWiG assessment reference is present on the validated official case page. This is an explicit absence, not a broken graph link.

G-BA decisions

Distinct actions and documents

1 decision

2025-06-18

discontinuation

Arzneimittel-Richtlinie/Anlage XII: Bulevirtid (Hepatitis-Delta-Virus (HDV)-Infektion, HDV-RNA-positiv, ≥ 3 bis < 18 Jahre, ≥ 10 kg KG) – Einstellung eines Verfahrens zur Nutzenbewertung

The G-BA issued a discontinuation on 2025-06-18. The official page states that it took effect as follows: 18.06.2025. 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

5 source
Generic graph relations · 3