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Immuron Ltd — Investor Presentation 2025
Aug 28, 2025
35121_rns_2025-08-28_6504bbbe-a59c-4728-bb47-bf00e54c2c49.pdf
Investor Presentation
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NASDAQ: IMRN ASX: IMC
FY25 Results Presentation
Steven Lydeamore Chief Executive Officer
SAFE HARBOR STATEMENT
Certain statements made in this presentation are forward-looking statements and are based on Immuron’s current expectations, estimates and projections. Words such as “anticipates,” “expects,” “intends,” “plans,” “believes,” “seeks,” “estimates,” “guidance” and similar expressions are intended to identify forward-looking statements.
Although Immuron believes the forward-looking statements are based on reasonable assumptions, they are subject to certain risks and uncertainties, some of which are beyond Immuron’s control, including those risks or uncertainties inherent in the process of both developing and commercializing technology. As a result, actual results could materially differ from those expressed or forecasted in the forward-looking statements.
The forward-looking statements made in this presentation relate only to events as of the date on which the statements are made. Immuron will not undertake any obligation to release publicly any revisions or updates to these forward-looking statements to reflect events, circumstances or unanticipated events occurring after the date of this presentation except as required by law or by any appropriate regulatory authority.
FY2025 results in this presentation are subject to audit review.
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Executive summary Immuron Ltd (NASDAQ:IMRN) (ASX:IMC) is a globally integrated biopharmaceutical company focused on developing, and commercialising, oral immunotherapeutics for the treatment of gut mediated diseases
Company Overview
Three commercial products: Travelan® (traveller’s diarrhoea), Protectyn® and ProIBS (irritable bowel syndrome) Three clinical programs : Travelan®: IMC: Phase 2 CHIM trial (n=60) Travelan®: USU: Field Study (n=866) IMM-529 (CDI): IMC: preparing IND for Phase 2 trial (n=60)
Clinical:
Business Update
Travelan® (IMM-124E) Travelan® Uniformed Services University IMM-124E trial 100% of 866 participants have been randomized and deployed
Commercial:
Continued quarter on quarter growth of Travelan® ProIBS launch stock ordered
Travelan® (IMM-124E) Travelan® Uniformed Services University IMM-124E trial topline results anticipated in October 2025
IMM-529 (CDI): Immuron anticipates submission of Investigational New Drug (IND) by end of September 2025
IMM-986 (VRE): Colostrum manufactured for preclinical studies; assay development in progress
Results, Upcoming Milestones & Outlook
Continued quarter on quarter growth of Travelan® from growth drivers
FY25 Results:
FY25 Global Sales Revenue of A$7.3 million up 49% on prior year – North American Travelan® sales A$2.0 million up 76% on prior year
Australian launch of ProIBS 1Q CY2026
Clinical Development
Profit[1] from Hyperimmune products for FY25 was A$1.35m, the same as FY24; FY25 increased selling & marketing investment A$1.4m
Travelan® IMM-124E: 1H 2026: End of Phase 2 FDA meeting (Phase 2; n=60)
IMM-529 (CDI): Immuron anticipates FDA approval of IND in December 2025
1 Segment reporting; excludes Research & Development and Corporate segments.
Financial Snapshot
| Financial Snapshot | |
|---|---|
| Shares on Issue 268,219,973 |
|
| Total Options 13,540,315 |
|
| Last Traded Price IMC: A$0.068 |
|
| 52 week High/Low IMC: A$0.11/0.054 IMRN: $2.87/1.50 Market Cap IMC: A$18.23m Cash & Term Deposit (30 June 2025) – Excludes A$2.8m raised from US placement (July 2025) A$5.9m |
Major Shareholders
| Major Shareholders | |
|---|---|
| Holder Units % of CSO |
|
| BNY Mellon Asset Management 113,417,824 42.29 % |
|
| Authentics Australia Pty. Ltd. 5,500,000 2.05 % |
|
| Grandlodge 3,846,712 1.43 % |
|
| Management & Board 3,234,153 1.21 % |
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1. FINANCIAL & OPERATIONAL HIGHLIGHTS
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FY25 Financial Summary
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Global Sales Australian Sales North American
Revenue Revenue Sales Revenue
$7.3m $5.3m $2.0m
Up 49% Up 40% Up 76%
Cash + Term
EBITDA (ex-R&D) [1]
Gross Profit
Deposit
$(3.1)m
Margin
$5.9m (excludes
$2.1m
65.4% A$2.8m raised from
improvement
the US placement) [2]
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1 ex-R&D: add back research & development, less R&D Tax Incentive and R&D grants; 2 30 June 2025, as reported in Immuron’s Appendix 4E (Cash $2.83m; Term Deposit $3.04m) and excludes the A$2.8m raised from the US placement of 32.9m shares at the AUD equivalent of $0.0824 per share conducted on the Nasdaq:IMRN completed 17 July 2025. The shares were purchased by US investors from Immuron’s US At-The-Market ( ATM ) facility. The ATM facility has now been fully utilised.
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Travelan® continued strong sales growth
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Global
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+ FY2025 AUD$7.3 million up 49% on prior year
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Australia
+ FY2025 AUD$5.2 million up 40% on prior year
+ Secured core ranging in additional nine pharmacy banner
groups
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North America
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- FY2025 AUD$2.0 million up 76% on prior year
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- Strongest sales growth on amazon.com
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- Secured distribution in ten pharmacy/grocery retailers in Canada
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Global Year to Date Net Sales ($AUD)
$8,000,000
$7,000,000
$6,000,000
$5,000,000
$4,000,000
$3,000,000
$2,000,000
$1,000,000
$-
Jul - Sep Oct - Dec Jan - Mar Apr - Jun
FY24 FY25
6
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Commercial – Operational Highlights
2H FY25 and 1H FY24 2H FY24 1H FY25 Outlook
-
Travelan ® / Protectyn®
-
• • • • $2.36m global sales $2.55m global sales $4.00m global sales $3.29m global sales
-
• • • •
-
Revenue $1.87m Australia $1.87m Australia $2.89m Australia $2.36m Australia • • • • $0.48m North America $0.67m North America $1.11m North America $0.93m North America • Australia: 3,700 pharmacies; 27m
-
Marketing & • peopleCanada: 10,000 pharmacies; 39m Distribution people • USA: 342m people
-
ProIBS
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• Exclusive distribution of ProIBS® for • Purchase order placed with the treatment of symptoms related anticipated delivery in 3Q2025.
-
Highlights to IBS in Australia and New Anticipated product launch in 1Q Zealand. CY2026.
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2. CLINICAL DEVELOPMENT PROGRAM
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Revenue generating with a strong clinical development pipeline
| Indication | 30 August 2024 | 29 August 2025 |
|---|---|---|
| Traveller’s Diarrhoea |
Travelan® (IMM-124E) Phase 2 Clinical study topline data reported in March 2024 |
Clinical study report submitted to FDA inJanuary 2025 Awaiting Travelan® Uniformed Services University clinical trial topline results (anticipatedOctober 2025) before requesting end of Phase 2 meeting |
| Travelan® Uniformed Services University clinical trial reaches77% recruitment of 866 patients |
Travelan® Uniformed Services University clinical trial100%of participants have been randomized and deployed Quality review of study data initiated October 2025anticipated top line results |
|
| Clostridioides Difficile |
IMM-529 pre-IND submission to the FDA inJuly 2024 | Planning IMM-529 FDA IND submission by end ofSeptember 2025 Anticipated IMM-529 FDA approvalDecember 2025 |
| Vancomycin Resistant Enterococci |
New project (IMM-986) initiation of pre-clinical research collaboration with Monash University targeting Vancomycin Resistant Enterococci (VRE) Colostrum manufactured for preclinical studies. In Vitro method development initiated. |
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Status of product portfolio and key milestones
| Indication | Compound | Peak U.S. sales Precl |
inical Phase 1 |
Phase 2 | Phase 3 | Registration | Collaborator or Funding Source |
Collaborator or Funding Source |
Current Status |
Anticipated Dates | Anticipated Dates |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2H 2025 | 1H 2026 | ||||||||||
| Traveller's Diarrhoea | Travelan® | US$ 102 m | Uniformed Services University |
100% of 866 participants recruited |
Topline Data | ||||||
| IMM-124E | Completed | End of Phase 2 FDA meeting |
|||||||||
| Clostridioides Difficile | IMM-529 | US$ 400 m | Pre-IND submission to FDA |
IND submission to FDA |
IND FDA approval (31 December 2025) |
||||||
| Vancomycin Resistant Enterococci |
IMM-986 | Manufacturing completed |
Preclinical activities |
In Vitro and In Vivo Preclinical data |
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3. UPCOMING MILESTONES & OUTLOOK
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Upcoming Milestones & Outlook
Commercial
-
- Continued quarter on quarter growth of Travelan® from growth drivers
-
- Australian launch of ProIBS in Q1 CY2026
-
- Planned growth in profitability[1] of Hyperimmune products net of planned increased investment in selling & marketing
Clinical
IMM-124E (Travelan®): Traveller’s Diarrhoea
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- IMM-124E: completed 100% recruitment, randomization and deployment
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(Phase 4; n=866)
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- IMM-124E: October 2025: Topline data (Phase 4; n=866)
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- IMM-124E: 1H 2026: End of Phase 2 FDA meeting (Phase 2; n=60)
IMM-529: Clostridioides difficile infection (C.diff, CDI)
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- IMM-529: 30 September: FDA IND Submission
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- IMM-529: 31 December: FDA IND Approval
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1 Segment reporting; excludes Research & Development and Corporate segments.
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STEVEN LYDEAMORE CHIEF EXECUTIVE OFFICER IMMURON LIMITED CONTACT INFORMATION:
EMAIL: [email protected] PHONE: AUSTRALIA: +61 438 027 172
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