Overview

Extension Study of Efficacy and Safety of LTP001 in Pulmonary Arterial Hypertension Participants

Status:
Not yet recruiting
Trial end date:
2025-07-21
Target enrollment:
Participant gender:
Summary
The purpose of this study is to measure the long-term safety and efficacy profile of LTP001 in participants with pulmonary arterial hypertension (PAH). The study offers participants who had completed the CLTP001A12201 double-blind parent study in PAH an opportunity to receive LTP001 (whether they were on LTP001 or not). Unblinding of the treatment received in CLTP001A12201 is generally not needed, but can occur on request by the investigator.
Phase:
Phase 2
Details
Lead Sponsor:
Novartis Pharmaceuticals