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Clinical trialNCT01725269TerminatedPhase 2Interventional

Long-term Study of AIR001 in Subjects With WHO Group 1 Pulmonary Arterial Hypertension Who Completed AIR001-CS05

SponsorAires Pharmaceuticals, Inc.Enrollment17Pulmonary Arterial Hypertension
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The AIR001-CS05 study evaluated the safety and efficacy (effectiveness) of AIR001 over 16 weeks in subjects who have PAH. The purpose of the AIR001-CS06 study is to evaluate the intermediate / long-term safety of AIR001 in subjects who have completed the AIR001-CS05 study. Assessments to evaluate the effectiveness of the study drug will include measurements of exercise ability and evaluations of PAH disease symptoms.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

25 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Australia
  • St. Vincent'S Hospital

    Darlinghurst, New South Wales, Australia

  • the Prince Charles Hospital

    Chermside, Queensland, Australia

  • Royal Hobart Hospital

    Hobart, Tasmania, Australia

  • the Alfred Hospital

    Melbourne, Victoria, Australia

Hungary
  • Gottsegen Gyorgy Hungarian

    Budapest, Hungary

  • Semmelweis University

    Budapest, Hungary

  • University of Debrecen

    Debrecen, Hungary

  • University of Szeged

    Szeged, Hungary

United States
  • Ucsd Medical Center

    La Jolla, California, United States

  • Ucla Medical Center

    Torrance, California, United States

  • University of Colorado Denver

    Aurora, Colorado, United States

  • Kentuckiana Pulmonary Associates

    Louisville, Kentucky, United States

  • University of Maryland Medical Center

    Baltimore, Maryland, United States

  • Boston University School of Medicine

    Boston, Massachusetts, United States

  • Brigham and Women'S Hospital

    Boston, Massachusetts, United States

  • Tufts Medical Center

    Boston, Massachusetts, United States

  • Washington University School of Medicine

    St Louis, Missouri, United States

  • Duke University Medical Center

    Durham, North Carolina, United States

  • University of Cincinnati

    Cincinnati, Ohio, United States

  • the Ohio State University Medical Center

    Columbus, Ohio, United States

  • University of Pittsburgh Medical Center

    Pittsburgh, Pennsylvania, United States

  • University of Texas Southwestern Medical Center

    Dallas, Texas, United States

  • Adaani Frost, M.D.

    Houston, Texas, United States

  • Inova Fairfax Hospital

    Falls Church, Virginia, United States

  • Aurora St. Luke'S Medical Center

    Milwaukee, Wisconsin, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

AIR001
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Mar 2013
Primary completion
30 Apr 2014
Completion
30 Apr 2014
Last update posted
9 Apr 2014
Registered enrollment
17
Registry id
NCT01725269

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.