[A20-09] Dulaglutide (type 2 diabetes mellitus) - Benefit assessment according to §35a Social Code Book V

Last updated 04.05.2020

Project no.:
A20-09

Commission:
Commission awarded on 03.02.2020 by the Federal Joint Committee (G-BA).

Report type:
Dossier assessment

Status:
Commission completed

Department/Division:
Drug Assessment

Application field:
Digestion, metabolism and hormones

Indication/Intervention:

Adults with type 2 diabetes mellitus; monotherapy for patients in whom diet and exercise alone do not provide sufficient glycaemic control and for whom metformin is considered inappropriate due to intolerance or contraindications; combination therapy for patients in whom diet and exercise and the treatment with other blood-glucose lowering drugs do not provide sufficient glycaemic control

Result of dossier assessment:

Combination therapy for patients in whom diet and exercise and treatment with short-acting insulin (with or without another blood-glucose lowering drug) do not provide sufficient glycaemic control: hint of considerable added benefit if the treatment goal is a not near-normal blood glucose level. All other therapeutic indications and goals: added benefit not proven.

Note:

After completion of the assessment by IQWiG the Federal Joint Committee (G-BA) conducts a commenting procedure. This may provide supplementary information and as a result lead to a modified benefit assessment. Further information and the decision on the early benefit assessment can be found on the relevant page of the G-BA website.

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Accompanying information

Further information for consumers and patients is provided on IQWiG's health information website www.informedhealth.org.

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