Cases / 2025-07-15-D-1224
completed2025-07-15D series

Sepiapterin

Hyperphenylalaninämie bei Phenylketonurie

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Brand
Sephience
Manufacturer
PTC Therapeutics International Limited

G-BA action

final resolution

2026-01-22

Arzneimittel-​​​Richtlinie/Anlage XII: Sepiapterin (Hyperphenylalaninämie bei Phenylketonurie)

Evidence-checked summary

The G-BA found a hint of non-quantifiable added benefit for Erwachsene und pädiatrische Personen mit Phenylketonurie-assoziierter Hyperphenylalaninämie. The G-BA issued a final resolution on 2026-01-22. The official page states that it took effect as follows: 22.01.2026. 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 7657 →

Patient group

Erwachsene und pädiatrische Personen mit Phenylketonurie-assoziierter Hyperphenylalaninämie

Hint of non quantifiable added benefit

Comparator

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Official case record

What happened, in source order

No inferred stages

Consultation record

Oral hearing and Wortprotokoll

1 hearing

2025-11-24

55 parsed turns

Oral hearing: Sepiapterin (Hyperphenylalaninämie bei Phenylketonurie)

Official Wortprotokoll · 11 pages

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

2026-01-22

final resolution

Arzneimittel-​​​Richtlinie/Anlage XII: Sepiapterin (Hyperphenylalaninämie bei Phenylketonurie)

The G-BA found a hint of non-quantifiable added benefit for Erwachsene und pädiatrische Personen mit Phenylketonurie-assoziierter Hyperphenylalaninämie. The G-BA issued a final resolution on 2026-01-22. The official page states that it took effect as follows: 22.01.2026. 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

10 source
Generic graph relations · 7