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Our clinical trial portfolio is one of the largest in the country. We have more than 700 clinical trials open across 30 clinical units.

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665 clinical trials found
Clinical trials

Actair study

Patient Stratification and Monitoring of ACTAIR® Treatment Efficacy Using New Objective Immune Markers (Trial Not Registered)

Investigated initiated study - prospective controlled (three-arm) trial of 18 months of Actair (extended to 36 months total) whereby patients who had a clinical history of perennial rhinitis confirmed with a HDM skin prick of >5mm and serum HDM specific IgE > class 3 were recruited. Now a further extension of the study has been approved to include patients who are currently receiving a licensed house dust mite sublingual immunotherapy tablet (Actair or Acarizax) treatment for 2 or 3 years.
Coming soon

ADR

Australasian Dermatology Registry (Trial Not Registered)

The Australasian Dermatology Registry captures real world data to enable monitoring and surveillance of current and emerging treatments and provides a platform for dermatology research, helping dermatologists provide the best care to their patients. The Australasian Dermatology Registry is a national collaboration between dermatologists, facilitated and coordinated by the Skin Health Institute.
Currently recruiting

AF and sexual dysfunction

Assessing the impact of atrial fibrillation and catheter ablation on sexual function: an observational study (Trial Not Registered)

This study aims to ask patients about how their AF has affected intimate relationships and whether catheter ablation has any effect on this.
Currently recruiting

ALLAY-HFrEF

Safety and Efficacy of the Alleviant No-Implant Interatrial Shunt in Patients with Heart Failure and Reduced Ejection Fraction (NCT06812533)

This study is to evaluate the safety and efficacy of the Alleviant ALV1 System in patients with reduced ejection fraction (HFrEF), who remain symptomatic despite optimal maximally tolerated guideline directed medical therapy (GDMT).

Currently recruiting

Alpha Orbit - STAR0215-301

A Phase 3, Multicenter, randomised, double-blind, placebo controlled trial to evaluate the efficacy and safety of Navenibart in participants with Hereditary Angioedema (NCT06842823)

Navenibart is being developed as a prophylactic treatment for the prevention of Hereditary Angioedema attacks.

No longer recruiting

Alpha-9 GRPR Study

A Phase 1 Study Investigating the Safety, Tumor Uptake, Biodistribution, and Dosimetry of [68Ga]Ga-A9-6217 in Participants with Select Advanced or Metastatic Solid Tumors (ACTRN12625000268448)

A study is testing a new diagnostic product, to detect tumour tissue throughout the body using a radioactive substance a positron emission tomography (PET) tracer, that targets a protein Gastrin-Releasing Peptide Receptor (GRPR) which is found in various cancer types. This is not a treatment study. No treatment will be provided to you as part of this study. This study is testing a new imaging product only.

Currently recruiting