Researcher in lab

Find clinical trials

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

Clear filter
665 clinical trials found
Clinical trials

AMALTHEA AZD7798

A Double-blind, Placebo-controlled Phase IIa Study to Evaluate the Efficacy and Safety of AZD7798 in Patients with Moderate to Severe Crohns Disease [AMALTHEA] (NCT06450197)

This is a randomised, double-blind, parallel group, placebo-controlled Phase IIa study designed to evaluate the efficacy and safety of AZD7798 subcutaneous (SC) every 4 weeks (Q4W) in participants with moderate to severe Crohn’s disease. The objectives of this study will be evaluated in a broad Crohn’s disease population, and in predefined subpopulations, according to the areas of active inflammation (ileal/ileocecal [L1], colonic [L2], ileocolonic [L3]).

Currently recruiting

AMBER

Administration of the BCL-2 antagonist, venetoclax, to promote apoptosis of HIV-infected cells and reduce the size of the HIV reservoir: An investigator-initiated phase I/IIb clinical trial in people living with HIV on antiretroviral therapy. The AMBER Study. (NCT05668026)

AMBER is a clinical trial to investigate if venetoclax, a medication which promotes cell death (apoptosis), can promote cell death of long-lived HIV infected cells and lead to a reduction of the latent HIV reservoir. The first part in Denmark used different doses of venetoclax to establish the safest dose to use in people with HIV. The second part of the study is taking place both in Aarhus, Denmark and here in Melbourne, Australia. All participants in part 2 of the study will stay on their ART and receive 3 cycles of the optimal dose of venetoclax determined in the first part of the trial. These cycles are 28 days consisting of 14 days on treatment and 14 days off treatment.  The main outcome of the study is to determine the safety of venetoclax in people with HIV and then blood samples will be collected to understand if veneotclax has an effect on the size of the HIV reservoir and whether the drug is leading to the loss of HIV-infected cells.
Currently recruiting

AMGEN 20240361

A Phase 1b Open-label, Multicenter Study Evaluating the Safety, Tolerability, and Efficacy of Xaluritamig in Combination With Androgen Receptor Pathway Inhibitors in Participants With Metastatic Hormone-sensitive Prostate Cancer (NCT07140900)

The main objective of the trial is to evaluate the safety and tolerability of xaluritamig in combination with darolutamide or abiraterone.
Currently recruiting

ANZHIT-2 study

A multi-centre, Australian and New Zealand, phase II exploratory study of amendments to conditioning regimens in haplo-identical stem cell transplantation (ANZHIT-2) (ACTRN12622001232729)

This study (ANZHIT-2) aims to improve the treatment protocols in haploidentical (half match) transplants. We will be using more targeted chemotherapy and total body irradiation in the transplants thus improving on their safety and success. We will also compare the cost-effectiveness and quality of life of haploidentical transplants to matched donor transplants.
Currently recruiting