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Lead program: Phase II
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EmyriaASX: EMD

Data updated

2 Drug Candidates

Australian clinical-stage biotech pioneering psychedelic-assisted therapies. In 2025, Emyria became the first company in the world to commercially deliver MDMA-assisted psychotherapy for PTSD, with insurance funding secured from Medibank. Also operates a clinical trial division and an MDMA analogue discovery program in collaboration with the University of Western Australia.

Pipeline Intelligence

Developer Momentum

Programme tracker
Active candidates
2

All tracked candidates active

Active programmes
2

All tracked programmes active

Lead stage
Phase II

Multiple active stages

Forecast coverage
2 of 2

2 active programmes with forecast fields

Latest sourced update

ANZCTR ACTRN12623000838617 - MDMA-Assisted Therapy for PTSD

Jun 27, 2026 - Registry update - ANZCTR - MDMA (EMDMA-001)

Next known catalyst

Phase II topline

Timing not specified - MDMA (EMDMA-001) / EMDMA-001 Phase 2 Open-Label (PTSD, TGA Authorised) - Confidence: 50%

5 sources0 pipeline-linked trials0 pipeline-linked papers1 Phase II1 Preclinical

Development Programmes

2

MDMA (EMDMA-001)

Phase II

PTSD

Programme Tracker

PTSD

Primary: Australia (TGA)
Phase IIActive

Forecast

Phase II topline

Open-label 12-month MDMA-AT study at PAX Centre Perth; MDMA supply for up to 70 patients secured; national expansion underway

Milestones

Phase II started

Completed

Actual: Oct 1, 2023

First patient dosed in Australia under TGA-authorised MDMA-assisted therapy (Emyria/PAX Centre, Perth) — first approved MDMA dosing in Australian history

Why it matters: Emyria's October 2023 first dosing was the first legally authorised MDMA-assisted therapy session in history (the US MAPS Phase 3 was under FDA IND, Australia was the first to fully reschedule and permit therapy).

Phase II topline

Completed

Actual: Jun 1, 2024

Interim results: 8-patient cohort — all 8 showed improved outcomes; clinically and statistically significant PTSD symptom reduction and quality of life improvements

Why it matters: 100% response rate in initial cohort is a compelling interim signal, though the open-label design limits causal inference. Real-world data from Australia's first authorised MDMA therapy programme will be closely watched by regulators and clinicians globally.

Watch next: Full cohort results (up to 70 patients); health insurer pilot data; national expansion outcomes

Regulatory review accepted

Completed

Actual: Jul 1, 2023

TGA deschedules MDMA in Australia — first country to permit MDMA-assisted therapy

Why it matters: Australia's TGA rescheduling enabled the first government-authorised MDMA therapy programme globally, giving Emyria a first-mover advantage in the world's first regulated MDMA-AT market.

Regulatory review accepted

Completed

Actual: Mar 1, 2025

Expansion to second Empax Centre; first funded pilot programmes with health insurers launched; treatment-resistant depression programme added

Why it matters: Health insurer engagement is the critical commercialisation milestone — it moves MDMA-AT from out-of-pocket payments to mainstream healthcare coverage, potentially enabling population-level access.

Recorded Events

Mar 1, 2025: Regulatory review accepted

Jun 1, 2024: Phase II topline

Oct 1, 2023: Phase II started

Jul 1, 2023: Regulatory review accepted

Evidence Links

Emyria Recruits First Patient to MDMA-Assisted Therapy Trial

Press release - ASX / Emyria - Jul 10, 2023 - Verified

ASX release describes EMDMA-001 as evaluating safety, efficacy, and cost-effectiveness of MDMA-assisted therapy for PTSD.

ANZCTR ACTRN12623000838617 - MDMA-Assisted Therapy for PTSD

Registry update - ANZCTR - Jun 27, 2026 - Verified

Australian/New Zealand registry entry for MDMA-assisted psychotherapy in PTSD, aligned with Emyria’s Australian regulated access pathway work.

Emyria's PTSD Program Delivers Lasting Recovery

Press release - Emyria - Feb 2, 2026 - Verified

Recent update reports clinically significant 12+ month follow-up data from Emyria’s PTSD treatment program under Australian regulated access pathways.

MDMA Analogue Library (UWA Partnership)

Preclinical

PTSD / Parkinson's L-DOPA dyskinesia

Programme Tracker

PTSD

Primary: Australia (TGA)
Pre-clinicalActive

UWA/Emyria MDMA-analogue programme remains preclinical, with UWA 2025 award coverage confirming Emyria rights to the analogue library and initial Parkinson disease focus.

Milestones

Pre-clinical completed

In progress

Why it matters: Emyria's MDMA analogue library targets two distinct design goals: a faster-acting MDMA for PTSD therapy (reducing session time) and a non-psychoactive MDMA analog for Parkinson's L-DOPA dyskinesia (LID) — a novel and commercially underappreciated indication where serotonergic modulation may reduce the involuntary movements caused by L-DOPA therapy.

Watch next: Lead compound nomination from 150+ library and IND-enabling study initiation

Evidence Links

Emyria and UWA Partner to Commercialise Novel Serotonin-Releasing Agents

Press release - Investing News / Emyria - Jan 1, 2024 - Verified

Announcement supports exclusive UWA licence for serotonin-releasing agents targeting mental health and neurological conditions.

UWA Research Recognised in Innovator of the Year Awards

university-news - University of Western Australia - Nov 1, 2025 - Verified

UWA says Emyria secured rights to a library of more than 100 novel MDMA analogues created in Matt Piggott research group.

Similar Developers

Reference points selected from shared pipeline stage, indications, compounds, regulatory pathways, and evidence footprint.

View landscape
Biomind Labs
Phase II2 active candidates3 trials
same indication: Neurocognitive DisordersPhase II peer2 overlapping stagessimilar active pipeline size
Mydecine Innovations
Phase II2 active candidates
same indication: PTSDPhase II peer2 overlapping stagessimilar active pipeline size
Gilgamesh Pharma
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same indication: PTSDPhase II peer2 overlapping stagesboth have forecast coverage
Apex Labs
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same indication: PTSDPhase II peersimilar active pipeline sizeboth have forecast coverage

Quick Facts

Type
Public Biotech
Founded
2016
Ticker
ASX: EMD
Lead Stage
Phase II
Website
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