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orBec® is a registered trademark and Oraprine™, RiVax™, LPM™, LPE™, PLP™ and MicroVax™ are trademarks of Soligenix, Inc. Registrations exist in the United States and various countries throughout the world. Biothrax™ is a trademark of the Bioport Corporation. Imuran® is a registered trademark of Glaxo Wellcome. Taxol® is a registered trademark of Bristol-Myers Squibb. Lupron® is a registered trademark of TAP Pharmaceuticals, Inc. For more complete information regarding the status of a particular trademark in a particular country, please contact Soligenix.
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Please understand that when you access another website through this one, Soligenix can accept no responsibility for your experience with the site. In addition, a link to a non-Soligenix site does not mean that Soligenix endorses or recommends that site or its contents.
The information provided in the Investor Relations section of this site is provided through a hypertext link to a third party website. (See above for important information about links to third party websites.) Under no circumstances will Soligenix be liable for any loss or direct, indirect, incidental, special or consequential damages caused by reliance on this information or for the inherent risks of the stock market.
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Policy on Financial Conflicts of Interest (FCOI) in Public Health Service (PHS) Funded Research
This Policy implements Financial Conflicts of Interest (FCOI) disclosure requirements found in 42 CFR Part 50 and 45 CFR Part 94 which are applicable to Research funded by the U.S. Public Health Service. This regulation does not apply to Phase I Small Business Innovation Research (SBIR) or Small Business Technology Transfer (STTR) program applications or awards. As a condition for receiving PHS funding, these regulations require Soligenix to maintain an appropriate written policy on financial conflict of interest disclosure. These requirements are applicable to all Research projects for which Soligenix submits a proposal to or receives Research funding from PHS, except for Phase I SBIR or STTR Research projects, as noted above. Each Investigator, as defined in the Policy, that is planning to participate in, or is participating in such Research, must follow this process and complete the required training. Subcontractors/consultants who perform services within the definition of an Investigator must maintain a policy that complies with the aforementioned regulatory requirements or comply with this Policy. Questions regarding this Policy should be directed to Soligenix’s Institutional Official.
Consistent with these requirements, Soligenix’s Policy, Soligenix FCOI Disclosure Form (pdf) and required FCOI Disclosures are available. The FCOI Disclosure information is current as of October 12, 2012 and is subject to updates at least annually as well as within 60 days of Soligenix’s identification of a new Financial Conflict of Interest.
This website may contain forward-looking statements that reflect Soligenix, Inc.’s current expectations about its future results, performance, prospects and opportunities, including but not limited to, potential market sizes, patient populations and clinical trial enrollment. Statements that are not historical facts, such as “anticipates,” “estimates,” “believes,” “intends,” “potential,” or similar expressions, are forward-looking statements.
These statements are subject to a number of risks, uncertainties and other factors that could cause actual events or results in future periods to differ materially from what is expressed in, or implied by, these statements. Soligenix cannot assure you that it will be able to successfully develop, achieve regulatory approval for or commercialize products based on its technologies, particularly in light of the significant uncertainty inherent in developing vaccines against bioterror threats conducting preclinical and clinical trials of vaccines, obtaining regulatory approvals and manufacturing vaccines, that product development and commercialization efforts will not be reduced or discontinued due to difficulties or delays in clinical trials or due to lack of progress or positive results from research and development efforts, that it will be able to successfully obtain any further funding to support product development and commercialization efforts, including grants and awards, maintain its existing grants which are subject to performance requirements, enter into any biodefense procurement contracts with the US Government or other countries, that it will be able to compete with larger and better financed competitors in the biotechnology industry, that changes in health care practice, third party reimbursement limitations and Federal and/or state health care reform initiatives will not negatively affect its business, or that the US Congress may not pass any legislation that would provide additional funding for the Project BioShield program. These and other risk factors are described from time to time in filings with the Securities and Exchange Commission, including, but not limited to, Soligenix’s reports on Forms 10-Q and 10-K. Unless required by law, Soligenix assumes no obligation to update or revise any forward-looking statements as a result of new information or future events.
About Soligenix, Inc.
Located in Princeton, New Jersey, Soligenix, Inc. is a late-stage biopharmaceutical company developing products to treat life-threatening side effects of cancer treatments and serious gastrointestinal diseases, and vaccines for certain bioterrorism agents.
Through our BioDefense Division, the company is developing biomedical countermeasures pursuant to the Project BioShield Act of 2004. Specifically, Soligenix is developing stable bioengineered vaccines designed to protect against the deadly effects of ricin toxin, botulinum toxin and anthrax, all of which are considered serious bioterrorism threats.