TrialSignal
Clinical trial intelligence report
EXPEDITE: A 16-Week, Multicenter, Open-label Study of Remodulin Induction Followed by Orenitram Optimization in Subjects With Pulmonary Arterial Hypertension
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT03497689-Jul 28, 2026
NCT ID
NCT03497689
Status
COMPLETED
Phase
PHASE4
Sponsor
United Therapeutics
Executive brief
Investment-Ready Snapshot
EXPEDITE: A 16-Week, Multicenter, Open-label Study of Remodulin Induction Followed by Orenitram Optimization in Subjects With Pulmonary Arterial Hypertension is a PHASE4 clinical asset sponsored by United Therapeutics in Pulmonary Arterial Hypertension. SEO and diligence focus: Intravenous/Subcutaneous Treprostinil; Oral Treprostinil, endpoint relevance, enrollment feasibility, competitive positioning, readout timing and IP durability.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03497689
Indication
Pulmonary Arterial Hypertension
Modality
small molecule
Target
Intravenous/Subcutaneous Treprostinil; Oral Treprostinil
Intervention
Intravenous/Subcutaneous Treprostinil; Oral Treprostinil
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.