← Back to all trials
Not Yet Recruiting
NCT07748000
A Study of LIQ861 (Inhaled Treprostinil) in Adults With Systemic Sclerosis Who Have Symptomatic Raynaud's Phenomenon Attacks
Conditions: Raynaud's Phenomenon Secondary to Systemic Sclerosis
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: PHASE2
Enrollment: 75
Sponsor: Liquidia Technologies, Inc.
Summary
Systemic sclerosis (SSc) is a rare autoimmune disease in which many patients experience Raynaud's phenomenon (RP) - painful episodes where commonly fingers or toes change color and become painful, numb, or tingly, usually triggered by cold or stress. This open-label study is testing an inhaled powder form of treprostinil (LIQ861) to find out which doses can be taken safely and comfortably by adults with SSc who have frequent symptomatic RP attacks. About 75 adults will be randomly assigned (2 to 1) to either a dose-titration group or a fixed low-dose group. The study also explores whether treatment reduces the number, severity, and impact of RP attacks. The main goal is to identify tolerated dose(s).
Eligibility Criteria
Inclusion Criteria:
* Male or female ≥18 years of age
* Classification of SSc per the 2013 ACR/EULAR criteria.
* Diagnosis or history of Raynaud's phenomenon
* Minimum of 12 (maximum 100) symptomatic RP attacks documented in the ePRO diary over ≥4 separate days
Exclusion Criteria:
* ≥3 digital ulcers at screening; a new digital ulcer between screening and randomization; gangrene or amputation within 6 months; digital ulcer infection within 3 months.
* History of cervical/digital sympathectomy or hand botulinum toxin injections within 90 days (or planned during the study).
* Clinically significant bleeding risk, coagulation disorder, or platelet count \
Source: ClinicalTrials.gov (NCT07748000). StuddyBuddy aggregates publicly available trial information.