{"id":17467,"date":"2022-11-07T09:46:48","date_gmt":"2022-11-07T09:46:48","guid":{"rendered":"https:\/\/touchrespiratory.com\/?post_type=media_gallery&p=17467"},"modified":"2022-12-14T10:28:42","modified_gmt":"2022-12-14T10:28:42","slug":"marc-simon-chest-2022-clinical-benefits-with-a-higher-dose-of-liq861-in-pulmonary-arterial-hypertension-analysis-of-the-lti-301-clinical-trial","status":"publish","type":"media_gallery","link":"https:\/\/touchrespiratory.com\/pulmonary-hypertension\/conference-hub\/marc-simon-chest-2022-clinical-benefits-with-a-higher-dose-of-liq861-in-pulmonary-arterial-hypertension-analysis-of-the-lti-301-clinical-trial\/","title":{"rendered":"Marc Simon, CHEST 2022: Clinical benefits with a higher dose of LIQ861 in pulmonary arterial hypertension – analysis of the LTI-301 clinical trial"},"content":{"rendered":"
INSPIRE (LTI-301 clinical trial) was a phase 3 study investigating the long-term safety and tolerability of LIQ861 in patients with pulmonary arterial hypertension (NCT03399604<\/a>). touchRESPIRATORY were delighted to talk with Dr. Marc Simon<\/strong> (UCSF Health, San Francisco, CA, USA) around the aims, design and eligibility criteria of the LTI-301 clinical trial and the findings from his exploratory efficacy analysis of the study looking at clinical benefits with a higher dose of LIQ861.<\/p>\n