Ceretas Enrols First Patient in Phase 2 Ultrasound Alzheimer’s Trial

Ceretas has enrolled the first patient in its Ceretas CERE-CALM Alzheimer's trial, a 66-patient study testing whether a portable ultrasound device can ease dementia symptoms without drugs or surgery.
By Josua Ferreira -
  • Ceretas has enrolled the first patient in its CERE-CALM trial, moving the company from trial preparation into treating patients and collecting data.
  • The randomised, double-blind, sham-controlled study targets 66 patients, with a minimum of 60, and is expected to finish in the first half of calendar 2028.
  • The company calls the trial fully funded, with $3.4 million from its share offer set aside for it.
  • An earlier study of 12 patients found the ultrasound treatment fast, safe and well tolerated, with early signs of better behaviour symptoms.
  • Recruitment is open at one Sydney site, with St Vincent's Hospital and the John Hunter Medical Research Institute expected to start shortly.
Summarise with AI:

First patient enrolled in Ceretas Phase 2 CERE-CALM Alzheimer’s trial

Ceretas Limited (ASX:CTS) has enrolled the first patient in its Phase 2 CERE-CALM trial, a clinical milestone for its portable, non-invasive therapeutic ultrasound platform. The Phase 2 Alzheimer’s trial is evaluating low-intensity focused ultrasound neuromodulation for behavioural and psychological symptoms of dementia (BPSD).

The announcement, dated 29 October 2026, sets out the following trial parameters:

  • 66 patients targeted (minimum 60)
  • Randomised, double-blind, sham-controlled design
  • Trial described as fully funded
  • Completion anticipated in H1 CY28

The Company states that $3.4 million of its IPO proceeds is allocated to CERE-CALM.

Dr Rachel de las Heras, CEO/MD

“The enrolment of our first patient in CERE-CALM represents an important milestone for Ceretas as we advance our therapeutic ultrasound technology through clinical development.”

The company also noted that CERE-CALM is designed to build on Phase 1 findings through a larger, placebo-controlled study. For investors, enrolment moves Ceretas from trial preparation into active patient treatment and data generation.

Inside the CERE-CALM trial design

Trial structure and endpoints

CERE-CALM is a Phase 2 randomised, double-blind, sham-controlled trial. A sham procedure is a placebo, which allows researchers to compare outcomes between treated and untreated groups.

Feature Detail
Population Adults aged 50 and over with probable Alzheimer’s disease and BPSD
Randomisation 2:1 to active treatment or sham control
Treatment schedule Six treatments over 12 weeks: four weekly sessions followed by two monthly sessions
Primary endpoint Change in Neuropsychiatric Inventory (NPI) total score, baseline to week 6, active treatment versus sham control
Secondary endpoints Caregiver distress at week 6 and week 12, durability of treatment effect at week 12, and overall safety and tolerability

The trial is listed on the Australian and New Zealand public clinical trial registry under code ACTRN12626000738325.

Where recruitment is happening

Patient recruitment is underway at Cognivus Research in Sydney. Recruitment at St Vincent’s Hospital in Sydney and the John Hunter Medical Research Institute is expected to commence shortly.

Additional sites could support the pace of enrolment across the multi-site Australian study.

Understanding focused ultrasound neuromodulation and BPSD

Three concepts sit behind the trial.

  1. Neuromodulation: a technique used to influence the activity of nerves and neural circuits in the brain.
  2. How the technology works: Ceretas’ technology delivers low-intensity ultrasound waves through the skull to specific areas of the brain, without requiring surgery. It is designed to influence neural activity in targeted circuits and does not rely on medication to produce a therapeutic effect. It is being developed as a portable treatment platform.
  3. BPSD: behavioural and psychological symptoms of dementia, including agitation, aggression, anxiety, depression and apathy. They affect over 90% of patients with Alzheimer’s disease and are associated with increased hospitalisation and earlier admission to residential aged care.

The company describes an area of substantial unmet clinical need. It states that drug-based treatments can have limited effectiveness for certain symptoms and may be associated with significant side effects, particularly in older and more vulnerable patients.

Ceretas is investigating whether focused ultrasound neuromodulation could provide an additional, non-invasive treatment option. Any potential differentiation from drug-based approaches depends on safety and effectiveness being demonstrated.

Investment case: Phase 1 foundation and market opportunity

CERE-CALM follows a first-in-human Phase 1 study undertaken in 2024 by researchers at The University of Queensland’s Queensland Brain Institute (QBI). The study involved 12 patients with Alzheimer’s disease and found the treatment to be fast, safe and well tolerated, with preliminary signals of improvement in behavioural symptoms. The results were published in Brain Communications in December 2025.

The technology is based on more than a decade of research at The University of Queensland and QBI.

On market size, Alzheimer’s is the most common cause of dementia, which impacts 57 million people globally, with a new case diagnosed every 3 seconds.

The Ceretas device acts on brain tissue via two mechanisms: neuromodulation, and blood-brain barrier opening, which may facilitate clearance of disease-associated proteins and enhance delivery of therapeutic agents to the brain. CERE-CALM evaluates the neuromodulation approach for BPSD.

QBI researchers are separately running a Phase 2 AGIFUS trial (ACTRN12626000687392) evaluating the same technology in Alzheimer’s-related agitation. That trial is funded independently by Queensland Health and is distinct from CERE-CALM.

Ceretas is also progressing development of a next-generation therapeutic ultrasound device, supporting its longer-term objective of a scalable, non-invasive treatment platform for Alzheimer’s disease and other neurological conditions.

What happens next for Ceretas

Two stated milestones lie ahead.

  1. Additional site recruitment: recruitment at St Vincent’s Hospital in Sydney and the John Hunter Medical Research Institute is expected to commence shortly, as Ceretas progresses enrolment across the clinical sites.
  2. Trial completion: the trial is anticipated to complete in the first half of CY2028. Results are intended to inform the next stage of clinical development, including the design of subsequent studies and engagement with regulatory authorities regarding the requirements for potential approval.

The company describes CERE-CALM as fully funded, with $3.4 million of IPO proceeds allocated to the trial.

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Frequently Asked Questions

What is the Ceretas CERE-CALM Alzheimer's trial?

It is a Phase 2 trial testing low-intensity focused ultrasound on the behavioural and psychological symptoms of dementia, such as agitation and anxiety. It aims to enrol 66 adults aged 50 and over with probable Alzheimer's disease.

What is a sham-controlled trial?

In a sham-controlled trial, some patients get a fake treatment that looks real, which works like a placebo. Researchers then compare results between the treated group and the sham group.

When will the CERE-CALM trial results be available?

Ceretas expects the trial to finish in the first half of calendar 2028. The company says results will guide later studies and talks with regulators.

Where is the Ceretas Alzheimer's trial taking place?

Recruitment is underway at Cognivus Research in Sydney. St Vincent's Hospital in Sydney and the John Hunter Medical Research Institute are expected to start shortly.

How is the CERE-CALM trial being funded?

Ceretas describes the trial as fully funded, with $3.4 million of its share offer proceeds set aside for it.

Josua Ferreira
By Josua Ferreira
Partnership Director
Josua Ferreira holds a Bachelor of Commerce in Marketing and Advertising and brings a background in publication, business development, and ASX market storytelling. He has worked with listed companies across the resource sector and broader market, combining sharp commercial instincts with a genuine commitment to keeping investors informed.
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