An Expanded Access Study to Assess Treprostinil Palmitil Inhalation Powder (TPIP) for Participants With Pulmonary Arterial Hypertension (PAH) and Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)

Trial statusAvailable
Trial phaseNot listed
Trial typeExpanded Access
Biological sexAll
Age18+
SponsorInsmed Incorporated

About this trial

The purpose of this study is to provide continued access to TPIP for participants who have successfully completed the open-label extension (OLE) studies of INS1009-203 for PAH or INS1009-212 for PH-ILD.

Eligibility criteria

Qualifiers

The participant is ineligible for or cannot be treated satisfactorily with alternative commercially available therapy for PAH or PH-ILD.

Participant provides their informed consent to participate as per local requirements.

Participant must have successfully completed the OLE INS1009-203 or INS1009-212 studies.

Based on the treating physician's judgement on participant's medical history and an evaluation of the overall risk-benefit profile, the participant will be determined to be suitable for continued TPIP treatment within this program.

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Treprostinil Palmitil

Treatment groups

No treatment groups listed

Locations

This trial has no locations

Sponsors and collaborators