[A19-103] Dolutegravir/lamivudine (HIV infection) - Second Addendum to Commission A19-55

Last updated 06.03.2020

Project no.:
A19-103

Commission:
Commission awarded on 09.12.2019 by the Federal Joint Committee (G-BA).

Report type:
Addendum

Status:
Commission completed

Department/Division:
Drug Assessment

Application field:
Immune system and infections

Indication:

Adults with HIV-1 infection whose virus has no known or suspected resistance to integrase inhibitors or lamivudine

Result of dossier assessment:

Now hint of lesser benefit in comparison with continuation of ongoing therapy for pretreated adults with HIV-1 infection without indication for a treatment switch (before: added benefit not proven)

Note:

If the need for additional work on a project commissioned by the G-BA arises during consultations, then IQWiG presents a report in the form of an "addendum". The G-BA subsequently decides on the extent of the added benefit, thus completing the early benefit assessment.

Federal Joint Committee (G-BA)

2020-02-06 A G-BA decision was published.

G-BA documents on this decision

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