Full Press Release Details
NASH clinical trial presentation and
continued revenue growth
Australia, November 9, 2018: Immuron Limited (ASX: IMC; NASDAQ: IMRN), an Australian microbiome biopharmaceutical company focused
on developing and commercializing oral immunotherapeutics for the treatment of many gut mediated diseases, today announced that
the IMM-124E NASH clinical study findings will be presented by Professor Arun Sanyal at the American Association for the study
of Liver Disease which will be held in San Francisco, California during the 9th - 13th of November
The presentation entitled "IMM-124E
Improves Metabolic Endotoxemia and Markers of Liver Injury in Non-Alcoholic Steatohepatitis" will be on the 11th
of November 2018 at the Novel Therapeutics for NASH session. A copy of the presentation will be made available on Immuron's
website at www.immuron.com.
Travelan was on display at HealthEd, the
Australian General Practitioner conference series, in Sydney, Melbourne and Brisbane. At these events, Dr. Bernie Hudson, a respected
key opinion leader in Travel Medicine, presented the latest research on travellers' diarrhoea to an audience of over 2,000
medical professionals. Key research data on Travelan and its efficacy was included in this educational piece.
The company is pleased to report the sales
results of its commercially available and over-the-counter gastrointestinal and digestive health supplement Travelan ,
for the fiscal year first quarter ending on September 30, 2018.
Australian Travelan sales
reached $340K AUD in the first quarter of CY19, compared to $330K in the same period of last financial year. In the month of September
2018, Australian Travelan sales climbed to $142K AUD, showing a strong 20% increase from the same month of last financial year.
Global Immuron Limited revenue for Q1 CY2018,
reached $482K AUD before rebates, compared to $475K last financial year.
CEO Jerry Kanellos states "we are pleased that Professor Arun Sanyal will be sharing our clinical study findings at this
important meeting. The company's focus since reporting the topline results of the study in March this year has been
on completing the final clinical study report and we are currently working with our contract research organization partners to
complete the final analysis of the data generated, and additional tests currently being performed. The final clinical study report
should be completed by the end of this year and the plan is to submit it in the new year according to the FDA Code of Federal Regulations
(42 CFR Part 11) - Clinical Trials Registration and Result Information Submission guidelines."
Immuron Limited (ASX: IMC, NASDAQ: IMRN),
is an Australian microbiome biopharmaceutical company focused on developing and commercializing orally delivered targeted polyclonal
antibodies for the treatment of inflammatory mediated and infectious diseases. Immuron has a unique and safe technology platform
that enables a shorter development therapeutic cycle. The Company currently markets and sells Travelan for the
prevention of Travelers' Diarrhea and its lead clinical candidate, IMM-124E, is in Phase II clinical trials for Non-Alcoholic
Steatohepatitis (NASH), Severe Alcoholic Hepatitis (SAH) and Pediatric Nonalcoholic Fatty Liver Disease (NAFLD).
Immuron's second clinical stage asset, IMM-529, is targeting Clostridium difficile Infections (CDI). These
products together with the Company's other preclinical immunotherapy pipeline products targeting immune-related diseases
currently under development, will meet a large unmet need in the global immunotherapy market.
For more information visit: http://www.immuron.com.
FORWARD-LOOKING STATEMENTS:
This press release may contain "forward-looking
statements" within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act
of 1934, each as amended. Such statements include, but are not limited to, any statements relating to our growth strategy and product
development programs and any other statements that are not historical facts. Forward-looking statements are based on management's
current expectations and are subject to risks and uncertainties that could negatively affect our business, operating results, financial
condition and stock value. Factors that could cause actual results to differ materially from those currently anticipated include:
risks relating to our growth strategy; our ability to obtain, perform under and maintain financing and strategic agreements and
relationships; risks relating to the results of research and development activities; risks relating to the timing of starting and
completing clinical trials; uncertainties relating to preclinical and clinical testing; our dependence on third-party suppliers;
our ability to attract, integrate and retain key personnel; the early stage of products under development; our need for substantial
additional funds; government regulation; patent and intellectual property matters; competition; as well as other risks described
in our SEC filings. We expressly disclaim any obligation or undertaking to release publicly any updates or revisions to any forward-looking
statements contained herein to reflect any change in our expectations or any changes in events, conditions or circumstances on
which any such statement is based, except as required by law.