A I M I M M U N O . C O M N Y S E A M E R I C A N : A I M
Corporate Presentation
Forward-Looking Statements
Some of the statements included in this presentation may be forward-looking statements that involve a number of risks and uncertainties. Among other things, for those statements, we claim the protection of safe harbor for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995. Any forward-looking statements set forth in this presentation speak only as of the date of this presentation. We do not undertake to update any of these forward-looking statements to reflect events or circumstances that occur after the date hereof. We are in various stages of seeking to determine whether Ampligen will be effective in the treatment of multiple types of viral diseases, cancers, and immune-deficiency disorders and the presentation sets forth our current and anticipated future activities. These activities are subject to change for a number of reasons. Significant additional testing and trials will be required to determine whether Ampligen will be effective in the treatment of these conditions. Results obtained in animal models do not necessarily predict results in humans. Human clinical trials will be necessary to prove whether or not Ampligen will be efficacious in humans. No assurance can be given as to whether current or planned clinical trials will be successful or yield favorable data and the trials are subject to many factors including lack of regulatory approval(s), lack of study drug, or a change in priorities at the institutions sponsoring other trials. In addition, initiation of planned clinical trials may not occur secondary to many factors including lack of regulatory approval(s) or lack of study drug. Even if these clinical trials are initiated, we cannot assure that the clinical studies will be successful or yield any useful data or require additional funding. Some of the world's largest pharmaceutical companies and medical institutions are racing to find a treatment for COVID-19. Even if Ampligen proves effective in combating the virus, no assurance can be given that our actions toward proving this will be given first priority or that another treatment that eventually proves capable will not make our efforts ultimately unproductive. Even if Ampligen proves effective in combating the virus, no assurance can be given that our actions toward proving this will be given first priority or that another treatment that eventually proves capable will not make our efforts ultimately unproductive, as multiple vaccines are now available and major pharma companies are working to develop their own disease treatments. We recognize that all cancer centers, like all medical facilities, must make the pandemic their priority. Therefore, there is the potential for delays in clinical trial enrollment and reporting in ongoing studies. No assurance can be given that future studies will not result in findings that are different from those reported in the studies referenced in the presentation. Operating in foreign countries carries with it a number of risks, including potential difficulties in enforcing intellectual property rights. In addition, many countries, including Argentina, are dealing with COVID-19 outbreaks and have made that their primary focus. We believe that this may be delaying our commercialization of Ampligen in Argentina until COVID-19 is more under control. We cannot assure that our potential foreign operations will not be adversely affected by these risks.
Please review the "Risk Factors" section in our latest annual report on Form 10-K and subsequent quarterly reports on Form 10-Q. Our filings are available at www.aimimmuno.com. The information found on our website is not incorporated by reference into this presentation and is included for reference purposes only.
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Investor Highlights
We are an immuno-pharma company focused on the development of therapeutics to treat multiple types of cancers, viral diseases and immune-deficiency disorders
Lead program Ampligen is an immuno-modulator with broad spectrum activity potentially applicable in multiple high-value indications
Approved in Argentina as | Six (6) ongoing oncology | Antiviral studies, including |
safe and effective for the | clinical trials with multiple | COVID-19, either underway or in |
treatment of severe Chronic | data readouts expected over | development. Initial COVID-19 |
Fatigue Syndrome (CFS) | the next 6-12 months | clinical data expected by Q2 |
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Broad Oncology Pipeline Across High-Value Indications
Indications | Approach | Partner | Preclinical | Phase 1 | Phase 2 | Phase 3 | Approval |
Ovarian Cancer | Chemokine | ||
(Advanced, Recurrent) | Modulatory Regimen | ||
Colorectal Cancer | Chemokine | ||
(Metastatic) | Modulatory Regimen | ||
Breast Cancer | Chemokine Modulatory | ||
(Metastatic Triple-Negative) | Regimen / Pembrolizumab | ||
Ovarian Cancer | Combination: | ||
(Advanced, Recurrent) | Pembrolizumab | ||
Prostate Cancer | Combination: Intron A | ||
(Early-Stage) | |||
Pancreatic Cancer | Single Agent | EAP | |
Breast Cancer | Chemokine Modulatory | ||
(Early-Stage Triple- Negative) | Plus Neoadjuvant Chemo | ||
Pancreatic Cancer | Single Agent | ||
Melanoma | Combination: | Under Development | |
(Refractory) | Intron A | ||
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Extensive Viral and
Immune System Disorder Pipeline
Indications | Approach | Preclinical | Phase 1 | Phase 2 | Phase 3 | Approval |
Viral Infections | ||
COVID-19 in Cancer Patients | Combination: Interferon | |
Alpha-2b and Ampligen Alone | ||
Immune System Disorder | ||
Severe CFS | Single Agent | Approved in |
Argentina | ||
Planning 2nd Phase | ||
ME/CFS | Single Agent | |
3 Confirmatory Trial | ||
Long COVID-19* | Single Agent | |
Under | ||
Post-COVID-19 | Single Agent | |
Cognitive Impairment | Development | |
*included in ongoing ME/CFS trial | 5 |
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AIM ImmunoTech Inc. published this content on 26 January 2022 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 26 January 2022 14:36:08 UTC.