DAC Meeting Outcome

DAC Meeting Outcome - Feb 2026

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The HA Drug Advisory Committee (DAC), comprising doctors, clinical pharmacologists and pharmacists, systematically appraises new drugs every three months. DAC is supported by expert panels which provide specialist views on the selection of drugs for individual specialties.

Drug Advisory Committee February 2026 Meeting Outcome


 

Generic / Brand name

Meeting outcome

Primary reason for unsuccessful application1

1

Amivantamab (Rybrevant)

Unsuccessful

The justification of the treatment’s cost in relation to its benefits is insufficient

2

Belimumab (Benlysta)

Approved

 

3

Bempedoic acid (Nilemdo)

Approved

 

4

Bimekizumab (Bimzelx)

Pending

Pending further information

5

Brentuximab Vedotin (Adcetris)

Approved

 

6

Capivasertib (Truqap)

Unsuccessful

The justification of the treatment’s cost in relation to its benefits is insufficient

7

Elacestrant (Orserdu)

Unsuccessful

The justification of the treatment’s cost in relation to its benefits is insufficient

8

Empagliflozin (Jardiance)

Unsuccessful

Alternative(s) available in HADF with comparable benefits

9

Luspatercept (Reblozyl)

Approved

 

10

Marstacimab (Hympavzi)

Unsuccessful

The justification of the treatment’s cost in relation to its benefits is insufficient

11

Methoxyflurane (Penthrox)

Unsuccessful

Alternative(s) available in HADF with comparable benefits

12

Nintedanib (Ofev)

Approved

 

13

Pertuzumab / Trastuzumab (Phesgo)

Approved

 

14

Ranibizumab (Lucentis)

Approved

 

15

Repotrectinib (Augtyro)

Unsuccessful

The justification of the treatment’s cost in relation to its benefits is insufficient

16

Ruxolitinib (Jakavi)

Approved

 

17

Selpercatinib (Retsevmo)

Approved

 

18

Tislelizumab (Tevimbra)

Unsuccessful

Insufficient evidence to demonstrate significant clinical outcome benefits

19

Vutrisiran (Amvuttra)

Unsuccessful

The justification of the treatment’s cost in relation to its benefits is insufficient


1The evaluation embraces the principles of safety, efficacy and cost-effectiveness and takes into account other relevant factors, including international recommendations and practices, advance in technology, disease state, patient compliance, quality of life, actual experience in the use of drugs as well as views of professionals and patients groups.