TrialsWest

Current Studies

Breakthrough treatment starts here. Browse our open clinical trials across
Western Australia and find one that's right for you.

  • Recruiting

    Respiratory

    PROPEL-IPF

    A Phase 2 clinical trial evaluating an oral investigational medication for people with idiopathic pulmonary fibrosis (IPF).

    Condition

    Idiopathic Pulmonary Fibrosis

    Study Duration

    up to 36 weeks

    Location

    Spearwood

    Read more: PROPEL-IPF
  • Closed

    Respiratory

    Bronchiectasis | AIRTIVITY™ 

    Study testing a new oral medication for bronchiectasis to reduce flare-ups and improve symptoms.

    Condition

    Bronchiectasis

    Study Duration

    1.5 years

    Location

    Spearwood

    Read more: Bronchiectasis | AIRTIVITY™ 
  • Recruiting

    Respiratory

    Bronchiectasis | CSL787_2001

    The study aims to determine whether an inhalant medication can delay or reduce lung flare‑ups, improve quality of life, and remain safe and well tolerated.

    Condition

    Non-cystic Fibrosis Bronchiectasis

    Study Duration

    12 months

    Location

    Osborne Park

    Read more: Bronchiectasis | CSL787_2001
  • Recruiting

    Metabolic

    MASH | INI-822-001

    This early study is testing a new drug in people with a liver condition to check if it’s safe and how well people tolerate it. It also looks at how the drug moves through the body and what effects it has, using gradually increasing doses.

    Condition

    Metabolic Dysfunction-Associated Steatotic Liver Disease (MASH)

    Study Duration

    12 weeks

    Location

    Mandurah

    Read more: MASH | INI-822-001
  • Recruiting

    Respiratory

    COPD | PRESTO

    This study is testing different doses of a new medication to see how safe it is and how well it works compared to a placebo in people with moderate to very severe COPD.

    Condition

    Chronic Obstructive Pulmonary Disease (COPD)

    Study Duration

    6 months

    Location

    Osborne Park

    Read more: COPD | PRESTO
  • Recruiting

    Metabolic

    MASH | SYNERGY-Outcomes

    The main goal of this study is to see if two different drugs can protect people with a specific type of high-risk fatty liver disease from developing severe, life-threatening liver problems.

    Condition

    Metabolic Dysfunction-Associated Steatotic Liver Disease (MASH)

    Study Duration

    2.5 years

    Location

    Osborne Park

    Read more: MASH | SYNERGY-Outcomes
  • Recruiting

    Gastroenterology

    Haemochromatosis | FERROCLEAR

    This study is testing a new medicine called Vamfeport in adults with a genetic condition that causes the body to absorb too much iron

    Condition

    Hereditary Haemochromatosis

    Study Duration

    12 months

    Location

    Osborne Park

    Read more: Haemochromatosis | FERROCLEAR
  • Recruiting

    Respiratory

    COPD | THESEUS

    A study evaluating the efficacy, safety, and tolerability of a new drug in adults with inadequately controlled Chronic Obstructive Pulmonary Disease (COPD).

    Condition

    Chronic Obstructive Pulmonary Disease (COPD)

    Study Duration

    up to 1 year

    Location

    Osborne Park

    Read more: COPD | THESEUS
  • Recruiting

    Respiratory

    COPD | VIGILANT

    A clinical research study to evaluate an investigational drug as an add-on treatment for Chronic Obstructive Pulmonary Disease (COPD)

    Condition

    Chronic Obstructive Pulmonary Disease (COPD)

    Study Duration

    up to 3 years

    Location

    Mandurah

    Read more: COPD | VIGILANT
  • Recruiting

    Liver - Metabolic

    MASH | SF-CSP-002

    The purpose of this study is to test the effectiveness and safety of the investigational medication in the treatment of Metabolic Dysfunction-Associated Steatohepatitis (MASH) in at risk adults.

    Condition

    Metabolic Dysfunction-Associated Steatohepatitis (MASH)

    Study Duration

    34 weeks

    Location

    Spearwood, Osborne Park and Mandurah

    Read more: MASH | SF-CSP-002
  • Recruiting

    Cardiovascular

    Cardiovascular | PREVENT_HF

    Heart Failure D697300001 Prevent-HF Study

    Condition

    Heart Failure

    Study Duration

    Up to 2 years

    Location

    Osborne Park

    Read more: Cardiovascular | PREVENT_HF
  • Closed

    Otolaryngology

    Chronic Rhinosinusitis | CEREN-2

    EFC18419 / Ceren 2

    Condition

    Chronic Sinusitis

    Study Duration

    Up to 76 weeks

    Location

    Spearwood

    Read more: Chronic Rhinosinusitis | CEREN-2
  • Closed

    Respiratory

    CALM-2 | BUS-P3-02

    BUS-P3-02 / CALM-2 Study

    Condition

    Chronic Cough

    Study Duration

    Up to 71 weeks

    Location

    Spearwood

    Read more: CALM-2 | BUS-P3-02
  • Closed

    Respiratory

    COPD | AER-01-002

    A Phase 2a, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Fexlamose (AER-01) Inhalation Solution in the Treatment of Adults with Moderate to Severe Chronic Obstructive Pulmonary Disease

    Condition

    Chronic Obstructive Pulmonary Disease (COPD)

    Study Duration

    Up to 10 weeks

    Location

    Spearwood & Osborne Park

    Read more: COPD | AER-01-002

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