Disease

Pulmonary arterial hypertension (PAH)

27 orphan drug statuses21 medicines15 companies

Pulmonary arterial hypertension (PAH) counts as a rare disease in Switzerland: Swissmedic has granted 27 orphan drug statuses for this indication. A medicine receives the status when no more than 5 in 10,000 people in Switzerland are affected by the life-threatening or chronically debilitating disease (Art. 4 para. 1 let. a decies TPA).

21 medicines carry a Swissmedic authorisation number for it and 15 companies hold the status. The table below lists every published orphan indication with the date the status was granted.

Orphan designations

Swissmedic publishes one row per medicine and orphan indication: the indication in the wording of the decision, the date the status was granted and, where the status was withdrawn, the withdrawal date. The table below reproduces those rows unchanged and links every indication to the matching rare disease in the directory.

One row per orphan indication, exactly as Swissmedic publishes it.
Orphan indicationStatus grantedStatus withdrawn
Pulmonale arterielle Hypertonie25/09/2025Status active
Pulmonale arterielle Hypertonie (PAH)08/05/2024Status active
Traitement à long terme de l'hypertension artérielle pulmonaire (HTAP) chez les patients en classes fonctionelles II à III de l'OMS afin de réduire la morbidité et le risque de mortalité.18/12/2023Status active
Behandlung der pulmonalen arteriellen Hypertonie (PAH)28/08/2023Status active
Pulmonale arterielle Hypertonie (PAH)11/10/2022Status active
Behandlung der pulmonalen arteriellen Hypertonie26/06/2019Status active
Behandlung der pulmonalen arteriellen Hypertonie (PAH) der WHO-Funktionsklasse II und III zur Verbesserung der körperlichen Leistungsfähigkeit bei Erwachsenen.27/03/2019Status active
Langzeitbehandlung von primärer pulmonaler Hypertonie und pulmonal arterieller Hypertonie mit Bindegewebserkrankung bei Patienten mit NYHA III und IV (Einteilung nach der New Yorker Heart Association).27/03/2019Status active
Behandlung der pulmonalen arteriellen Hypertonie (PAH)18/01/2018Status active
Behandlung der pulmonalen arteriellen Hypertonie (PAH)08/09/2016Status active
Behandlung der pulmonalen arteriellen Hypertonie12/02/2016Status active
Behandlung der pulmonalen arteriellen Hypertonie und der chronisch thrombo-embolischen pulmonalen Hypertonie18/08/2015Status active
pulmonalen arteriellen Hypertonie08/10/2013Status active
Pulmonale arterielle Hypertonie (PAH)17/07/2012Status active
Pulmonale arterielle Hypertonie (PAH)17/07/2012Status active
Hypertension artérielle pulmonaire (WHO class I)23/03/2011Status active
Pulmonal-arterielle Hypertonie14/12/2010Status active
Pulmonale arterielle Hypertonie und idiopathische pulmonale Fibrose30/08/2010Status active
Behandlung der pulmonalen arteriellen Hypertonie und der chronischen thromboembolischen pulmonalen Hypertonie01/07/2010Status active
Behandlung der pulmonalen arteriellen Hypertonie und der chronischen thromboembolischen pulmonalen Hypertonie01/07/2010Status active
Behandlung der pulmonalen arteriellen Hypertonie und der chronischen thromboembolischen pulmonalen Hypertonie01/07/2010Status active
Behandlung der pulmonalen arteriellen Hypertonie09/02/2009Status active
Behandlung der pulmonalen arteriellen Hypertonie und der chronisch thromboembolischen pulmonalen Hypertonie.26/09/2007Status active
Behandlung der pulmonalen arteriellen Hypertonie und der chronisch thrombo-embolischen pulmonalen Hypertonie07/05/2007Status active
Behandlung der pulmonalen arteriellen Hypertonie und der chronisch thrombo-embolischen pulmonalen Hypertonie07/05/2007Status active
Behandlung der pulmonalen arteriellen Hypertonie und der chronisch thromboembolischen pulmonalen Hypertonie07/05/2007Status active
Behandlung der pulmonalen arteriellen Hypertonie und der chronisch thromboembolischen pulmonalen Hypertonie07/05/200725/01/2010

Medicines

Reimbursement

Whether compulsory health insurance pays for this medicine depends on the FOPH specialities list (SL). Medicines that are not listed can be reimbursed case by case under Art. 71a-71d KVV.

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Care in Switzerland

Switzerland concentrates rare-disease care in the centres recognised by kosek. Patient organisations are networked through ProRaris, and the Orphanet database maintains Swiss entries.

Frequently asked questions

Which medicines with orphan drug status are available in Switzerland for Pulmonary arterial hypertension (PAH)?

Swissmedic lists 21 medicines with orphan drug status for this indication, among them Adcirca, Adempas junior, Adempas, Ambrisentan OrPha, Bosentan-Mepha. The full list with authorisation number and date is in the table on this page.

Does Swiss health insurance cover the treatment?

A medicine is reimbursed once it is on the FOPH specialities list (SL). Without an SL listing, or for use outside the limitation, reimbursement in an individual case under Art. 71a to 71d KVV is possible: the insurer decides after consulting its medical adviser, normally within two weeks.

Where are patients treated in Switzerland?

Care is delivered by the rare-disease centres recognised by kosek at the university and cantonal hospitals. Patient organisations are united in the ProRaris alliance, and diagnoses and reference centres are documented in Orphanet.

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Bring your orphan drug to Switzerland

You can enquire about orphan drug status, authorisation and reimbursement in Switzerland. Any specialist service and its scope are agreed separately with the external partner.

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