Latvia Squeezes Access for 123,000 Patients Out of Price Deals as 124 Drugs Wait
Latvia’s National Health Service (NVD) told the Saeima public health subcommittee on 29 September that reimbursement widens from 1 October, with capecitabine covered for solid tumours at any site, spinal muscular atrophy therapy extended to adults and adalimumab made a first-line biologic in moderate to severe Crohn’s disease and ulcerative colitis. Family doctors can now start dementia treatment, direct oral anticoagulants and GLP-1 receptor agonists. NVD said the gains came largely from manufacturer participation, price negotiations and internal savings rather than new funding, while forecasting higher reimbursement spending than last year on seven months of data.
Latvia is buying access with manufacturers’ money. NVD credits most of this round to manufacturer participation and price negotiation, inside a reimbursement budget it already expects to overrun. For any company with a product in the 124-medicine queue, the entry ticket is a commercial offer.
- Spend per patient is what the budget office sees. Reimbursement spending rose 94% from 2018 to 2025, from €175.21 million to €339.48 million, while unique patients rose 6% to 760,047. Every new inclusion adds cost per patient, which is why each one is now negotiated against budget impact.
- Primary care initiation is the commercial lever in this round. From 1 October family doctors can start GLP-1 receptor agonists, direct oral anticoagulants and dementia treatment without a specialist visit, which NVD says will speed treatment starts. For those classes, field force targeting and volume forecasts should shift toward general practice now.
- The 2027 budget decides the queue. The health ministry has identified €130.3 million in additional need for reimbursed medicines within €663 million of total need, but has prioritised €319.5 million for 2027. Until funding moves, expect inclusion on stepwise criteria and price concessions, the route NVD describes for chronic migraine.
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