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.

Find Melbourne Sexual Health Centre research studies and clinical trials

Data source: Bayside Health Alfred Powertrials list of active trials
Last updated: 3 September 2026

Clear filter
682 clinical trials found
Clinical trials

ATIS

Antigen Triggers in Inflammatory Skin-disease (Trial Not Registered)

The study aims to enrol 150 people with inflammatory skin conditions such as psoriasis. The study will collect samples from volunteers. These will be used to try and understand the role of antigen presentation in people with these diseases. Specifically, the research aims to identify pathogenic peptides in lesional vs. Non lesional skin. This could lead to more personalised and effective treatments for psoriasis and ultimately improve patient care.
Currently recruiting

BAF_FRontier-1

BAF_FRontier-1, A First-in-Human, Phase 1 Trial to Assess Safety, Tolerability, and Preliminary Efficacy of LY4152199, a B-cell Activation Factor Receptor [BAFF-R] T-Cell Engager Bispecific Antibody, in Adult Participants with Previously Treated B-cell Malignancies (NCT07101328)

LY4152199 is a human BAFF-R×CD3 bispecific antibody that engages BAFF-R on the surface of B-cells and CD3 on the surface of T-cells, with the goal of T-cell-mediated elimination of BAFF-R expressing malignant B-cells. Cohort A will assess the safety, tolerability, PK, and preliminary efficacy of escalating doses of LY4152199, administered via intravenous (IV) infusion, in participants with select relapsed/refractory B-cell malignancies. Cohort B will further assess the safety, tolerability, PK, and preliminary efficacy of LY4152199 in participants with relapsed/refractory diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL).
Coming soon

BEACON

A Phase 2/3 Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Investigate the Safety and Efficacy of Oral Brepocitinib in Adults with Cutaneous Sarcoidosis (NCT06978725)

This is a 16-week double blind study to evaluate the safety and effectiveness of an oral investigational study drug in adults with cutaneous sarcoidosis (CS), a condition where inflammatory disease affects the skin. Eligible participants will be randomly assigned to receive the study drug or placebo for 16 weeks. After this period, all participants will receive the study drug for 36 weeks. What is involved? A screening period of up to 30 days to check eligibility; A 16-week treatment period where participants receive either the study drug or placebo; A 36-week open-label extension period where all participants receive the study drug; A 4-week safety follow-up after treatment ends; Regular clinic visits for safety checks and physical assessments; Possible tapering of oral corticosteroids during the study, if applicable; Blood and urine tests to monitor safety and treatment response; Completion of questionnaires and clinical assessments related to skin disease and quality of life.
Coming soon