<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(5)</volume><submitter>Boettcher M</submitter><funding>Bayer</funding><funding>Merck</funding><funding>Merck Sharp and Dohme</funding><pubmed_abstract>Vericiguat was developed for the treatment of symptomatic chronic heart failure (HF) in adult patients with reduced ejection fraction who are stabilized after a recent decompensation event. Guidelines recommend long-acting nitrates, such as isosorbide mononitrate, for angina prophylaxis in chronic coronary syndromes (CCS), common comorbidities in HF. This study evaluated safety, tolerability, and the pharmacodynamic (PD) interaction between co-administered vericiguat and isosorbide mononitrate in patients with CCS. In this phase Ib, double-blind, multicenter study, patients were randomized 2:1 to receive vericiguat plus isosorbide mononitrate (n = 28) or placebo plus isosorbide mononitrate (n = 13). Isosorbide mononitrate was uptitrated to a stable dose of 60 mg once daily, followed by co-</pubmed_abstract><journal>Clinical and translational science</journal><pagination>1204-1214</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9099120</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Vericiguat in combination with isosorbide mononitrate in patients with chronic coronary syndromes: The randomized, phase Ib, VISOR study.</pubmed_title><pmcid>PMC9099120</pmcid><pubmed_authors>Dungen HD</pubmed_authors><pubmed_authors>Schulz-Burck D</pubmed_authors><pubmed_authors>Hung J</pubmed_authors><pubmed_authors>Mikus G</pubmed_authors><pubmed_authors>Werner N</pubmed_authors><pubmed_authors>Boettcher M</pubmed_authors><pubmed_authors>Karakas M</pubmed_authors><pubmed_authors>Gerrits M</pubmed_authors><pubmed_authors>Besche N</pubmed_authors><pubmed_authors>Donath F</pubmed_authors><pubmed_authors>Becker C</pubmed_authors><pubmed_authors>Trenk D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Vericiguat in combination with isosorbide mononitrate in patients with chronic coronary syndromes: The randomized, phase Ib, VISOR study.</name><description>Vericiguat was developed for the treatment of symptomatic chronic heart failure (HF) in adult patients with reduced ejection fraction who are stabilized after a recent decompensation event. Guidelines recommend long-acting nitrates, such as isosorbide mononitrate, for angina prophylaxis in chronic coronary syndromes (CCS), common comorbidities in HF. This study evaluated safety, tolerability, and the pharmacodynamic (PD) interaction between co-administered vericiguat and isosorbide mononitrate in patients with CCS. In this phase Ib, double-blind, multicenter study, patients were randomized 2:1 to receive vericiguat plus isosorbide mononitrate (n = 28) or placebo plus isosorbide mononitrate (n = 13). Isosorbide mononitrate was uptitrated to a stable dose of 60 mg once daily, followed by co-</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-05-09T23:39:02.78Z</modification><creation>2025-04-04T19:33:03.672Z</creation></dates><accession>S-EPMC9099120</accession><cross_references><pubmed>35299288</pubmed><doi>10.1111/cts.13238</doi></cross_references></HashMap>