Send to

Choose Destination
N Engl J Med. 2013 Jul 25;369(4):330-40. doi: 10.1056/NEJMoa1209655.

Riociguat for the treatment of pulmonary arterial hypertension.

Collaborators (139)

Bortman G, Keogh A, Kermeen F, Feenstra J, Williams T, Reeves G, Kilpatrick D, Lang I, Kahler C, Mascherbauer-Steringer R, Vachiery JL, Delcroix M, Meyer G, Arakaki J, Santana M, Waetge D, Granton J, Langleben D, Helmersen D, He J, Jing Z, Zhou D, Huang Y, Wang C, Jansa P, Neilsen-Kudsk JE, Hachulla E, De Groote P, Frachon I, Bourdin A, Pison C, Bauer F, Dromer C, Marquette CH, Degano B, Neurohr C, Wilkens H, Hoffken G, Hoeper M, Ghofrani A, Wirtz H, Rosenkranz S, Grünig E, Ewert R, Orfanos S, Kramer M, Ben Gal T, Scelsi L, Vizza C, Harari S, Confalonieri M, Albera C, Fukumoto Y, Sano M, Hatano M, Saji T, Tanaka S, Takeda Y, Takehara K, Matsubara H, Kihara Y, Shiohira Y, Kawai H, Homma S, Satoh T, Tokunaga T, Ishizaki T, Diaz C, Zamudio T, De Los Rios M, Estupian S, Cacho JR, Gamba M, Beckert L, Torbicki A, Castro G, Reis A, Agapito A, Martins S, Kim H, Lee S, Chang H, Song Y, Chazova I, Moiseeva O, Lim S, Yip J, Barbera J, Roman A, Palma Jdel C, Reitan O, Soderberg S, Jansson K, Speich R, Hsu HH, Lin HY, Cheng CC, Phrommintikul A, Jaimchariyatam N, Sayin T, Kultursay H, Ongen G, Pepke-Zaba J, Coghlan G, Peacock A, Gibbs J, Wagoner L, Badesch D, Frost A, Hill N, Allen R, Waxman A, Sood N, Torres F, Minai O, Shapiro S, Klinger J, Engel P, Garcia H, Schuller D, Poch D, Rosenzweig E, McConnell J, Rischard F, Ghofrani HA, Galiè N, Grimminger F, Humbert M, Keogh AM, Langleben D, Rubin LJ, Olschewski H, Haverkamp W, Lehmacher W, Hoischen S, Collamati S, Dehay J, Hallmann M, Menezes F.

Author information

University of Giessen and Marburg Lung Center, Giessen, Germany.



Riociguat, a soluble guanylate cyclase stimulator, has been shown in a phase 2 trial to be beneficial in the treatment of pulmonary arterial hypertension.


In this phase 3, double-blind study, we randomly assigned 443 patients with symptomatic pulmonary arterial hypertension to receive placebo, riociguat in individually adjusted doses of up to 2.5 mg three times daily (2.5 mg-maximum group), or riociguat in individually adjusted doses that were capped at 1.5 mg three times daily (1.5 mg-maximum group). The 1.5 mg-maximum group was included for exploratory purposes, and the data from that group were analyzed descriptively. Patients who were receiving no other treatment for pulmonary arterial hypertension and patients who were receiving endothelin-receptor antagonists or (nonintravenous) prostanoids were eligible. The primary end point was the change from baseline to the end of week 12 in the distance walked in 6 minutes. Secondary end points included the change in pulmonary vascular resistance, N-terminal pro-brain natriuretic peptide (NT-proBNP) levels, World Health Organization (WHO) functional class, time to clinical worsening, score on the Borg dyspnea scale, quality-of-life variables, and safety.


By week 12, the 6-minute walk distance had increased by a mean of 30 m in the 2.5 mg-maximum group and had decreased by a mean of 6 m in the placebo group (least-squares mean difference, 36 m; 95% confidence interval, 20 to 52; P<0.001). Prespecified subgroup analyses showed that riociguat improved the 6-minute walk distance both in patients who were receiving no other treatment for the disease and in those who were receiving endothelin-receptor antagonists or prostanoids. There were significant improvements in pulmonary vascular resistance (P<0.001), NT-proBNP levels (P<0.001), WHO functional class (P=0.003), time to clinical worsening (P=0.005), and Borg dyspnea score (P=0.002). The most common serious adverse event in the placebo group and the 2.5 mg-maximum group was syncope (4% and 1%, respectively).


Riociguat significantly improved exercise capacity and secondary efficacy end points in patients with pulmonary arterial hypertension. (Funded by Bayer HealthCare; PATENT-1 and PATENT-2 numbers, NCT00810693 and NCT00863681, respectively.).

[Indexed for MEDLINE]
Free full text

Supplemental Content

Full text links

Icon for Atypon
Loading ...
Support Center