Interstitial Lung Disease Clinical Trials in Cincinnati, Ohio

5 studies are recruiting for interstitial lung disease in Cincinnati, Ohio right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.

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Studies now recruiting

  1. DeciPHer-ILD: A Real-world Patient Registry in Group 3 Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)

    This is a prospective, real world, multicenter, registry of patients with pulmonary hypertension associated with interstitial lung disease (PH-ILD) and interstitial lung disease (ILD).

    Stage
    Not phased
    Ages
    18 and older
    Site
    University of Cincinnati Medical Center, Cincinnati, Ohio
    Locations
    71 in total
    Run by
    United Therapeutics
  2. Efficacy and Safety Study of Treprostinil Palmitil Inhalation Powder (TPIP) in Participants With Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)

    The primary objective of this study is to evaluate the effect of 24-weeks of once daily treatment with TPIP versus placebo on exercise capacity in adults with PH-ILD.

    Stage
    Phase 3
    Ages
    18 and older
    Site
    USA015, Cincinnati, Ohio
    Locations
    145 in total
    Run by
    Insmed Incorporated
  3. Abatacept for the Treatment of Common Variable Immunodeficiency With Interstitial Lung Disease

    There is no standard of care therapy for patients with granulomatous-lymphocytic interstitial lung disease (GLILD) seen in common variable immunodeficiency (CVID). Abatacept has recently looked promising for the treatment of patients with complex CVID. This study is a multi-site, phase II, randomiz…

    Stage
    Phase 2
    Ages
    4 and older
    Site
    Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio
    Locations
    6 in total
    Run by
    Children's Hospital Medical Center, Cincinnati
  4. Study of the Efficacy and Safety of Inhaled Treprostinil in Subjects With Progressive Pulmonary Fibrosis (TETON-PPF)

    Study RIN-PF-305 is designed to evaluate the safety and efficacy of inhaled treprostinil in subjects with progressive pulmonary fibrosis (PPF) over a 52-week period.

    Stage
    Phase 3
    Ages
    18 and older
    Site
    University of Cincinnati Medical Center, Cincinnati, Ohio
    Locations
    165 in total
    Run by
    United Therapeutics
  5. An Open-Label ProSpective MultiCENTer Study to Evaluate Safety and Tolerability of Dry Powder Inhaled Treprostinil in PH

    Study LTI-401 is an open-label, multicenter study which will evaluate the safety and tolerability of LIQ861 in subjects who have WHO Group 1 \& 3 PH.

    Stage
    Not phased
    Ages
    18 to 80
    Site
    University of Cincinnati Health, Cincinnati, Ohio
    Locations
    23 in total
    Run by
    Liquidia Technologies, Inc.

How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.

What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.

Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.