Pharmacoeconomic review report: Riociguat (Adempas)

Riociguat (Adempas) is a soluble guanylate cyclase (sGC) stimulator indicated for the treatment of pulmonary arterial hypertension (PAH, World Health Organization [WHO] Group 1), as monotherapy or in combination with endothelin receptor antagonists (ERAs) in adult patients (≥ 18 years of age) with W...

Full description

Bibliographic Details
Corporate Author: Canadian Agency for Drugs and Technologies in Health
Format: eBook
Language:English
Published: [Ottawa, Ontario] Canadian Agency for Drugs and Technologies in Health December 2015, 2015
Series:CADTH common drug review
Subjects:
Online Access:
Collection: National Center for Biotechnology Information - Collection details see MPG.ReNa
Description
Summary:Riociguat (Adempas) is a soluble guanylate cyclase (sGC) stimulator indicated for the treatment of pulmonary arterial hypertension (PAH, World Health Organization [WHO] Group 1), as monotherapy or in combination with endothelin receptor antagonists (ERAs) in adult patients (≥ 18 years of age) with WHO functional class II or III pulmonary hypertension. It is available in 0.5 mg, 1 mg, 1.5 mg, 2 mg, and 2.5 mg oral tablets, with a recommended dose of 1 to 2.5 mg three times daily, based on a 0.5 mg incremental titration phase. The manufacturer submitted a price of $42.75 per tablet for all dosage strengths based on its current list price, which corresponds to a cost of $128.25 daily per patient or $46,811 annually per patient. The manufacturer is requesting riociguat to be listed for patients who are unable to achieve disease control with another PAH therapy. Riociguat is also indicated for the treatment of inoperable chronic thromboembolic pulmonary hypertension (CTEPH, WHO Group 4) and persistent or recurrent CTEPH after surgical treatment in adult patients (≥ 18 years of age) with WHO functional class II or III pulmonary hypertension. Riociguat was previously reviewed for this indication (at the same submitted price) and received a "list with conditions" recommendation by the CADTH Canadian Drug Expert Committee (CDEC) in July 2014, one of which was the requirement of a substantial reduction in price
Physical Description:1 PDF file (ii, 17 pages) illustrations