ABOUT US


Plex Pharmaceuticals is a scientifically-driven company with a vision to improve the lives of patients diagnosed with complex, degenerative diseases. Plex Pharmaceuticals is focused on the treatment of diseases generally caused by  protein mis-folding such as ALS, Parkinson's Disease and cataracts.

Plex has a rich pipeline of drug discovery programs and a dedicated scientific team.  To date, Plex Pharmaceuticals has been primarily funded through grants from the NIH and the MJFF. Plex’s drug discovery lab and operations are located in San Diego, California.

 

  • Company founded in 2009.

  • Acquired by Collidion, Inc. in 2017.

Plex (Latin for fold) pharmaceuticals (formerly CalAsia Pharmaceuticals) is an early stage biotechnology company which is focusing its drug discovery expertise on diseases caused by protein misfolding: ALS, Parkinson’s disease and cataracts. CalAsia Pharmaceuticals, the predecessor to Plex Pharmaceuticals, was founded in 2009 and raised almost $3,000,000 in non-dilutive funding from the NIH and the Michael J.Fox Foundation to support its efforts in fragment-based screening and structure-based drug design. Plex pharmaceuticals additionally has a development program for Dengue, West Nile and Zika antiviral drugs which has also received support from the NIH and has worked on a novel brain-penetrant heat shock protein 90 (HSP90) inhibitor for glioblastoma.

MANAGEMENT


 
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Hoji Alimi, Chairman, CEO

Mr. Alimi has over 20 years of experience in the healthcare industry and has raised more than $170 million in capital throughout his career for different ventures. In 1999, he founded Micromed Laboratories Inc. to assist drug and device companies to navigate FDA and European Conformity (“CE”) mark approval processes. In 2002, Mr. Alimi founded Oculus Innovative Sciences, Inc., a company focused on topical anti- infective drugs as well as device-related applications. As CEO and Chairman, he led the company to successfully complete a randomized, double-blind, controlled phase II trial for improvement or cure of infection in diabetic ulcers.  Under his tenure, the company became publicly traded on Nasdaq and achieved dozens of regulatory approvals, including CE marks and 510(K) FDA clearances. In 2012, he founded Ruthigen, Inc. to focus on the development of a drug compound for the reduction of hospital acquired infections during invasive abdominal procedures. As CEO, Chairman and CSO, Ruthigen, Inc. completed an initial public offering and traded on NASDAQ, and later merged with Pulmatrix, a pulmonary-focused pharmaceutical company. Hoji Alimi holds more than 30 patents in areas of anti-infective, surgical, wound care and manufacturing of specific drugs and devices.   He received his B.A. in Biology - Sonoma State University 1995


 
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William H. Watson, III, Vice-President of Business Development

William Watson’s career stems from over 30 years in finance and has grown to provide pivotal business development strategy and implementation for Collidion, Inc. Mr. Watson has been a registered representative and registered principal with FINRA since the early 1980’s. From 2003 to 2007, he joined Brookstreet Securities as the Vice President of Corporate Finance, where he completed 21 engagements totaling over $250 million of private placements, PIPE transactions, initial public offerings, and secondary offerings for small capitalization growth companies.  He has completed an additional $100 million of financing in his career for a variety of other ventures. In addition to financing activities, he also assisted in the assembly of Collidion’s scientific advisory board, interfaced with the board of directors and management, and generated key business development leads with healthcare partners. Since 2013, Mr. Watson has served on the Board of Directors of the National Investment Bankers Association.


 

Sameer Harish, Director of Finance

Mr. Harish served as principal of Harish Life Science Advisors since 2011, an independent consulting firm he founded that provided financial, strategic and market research advisory services to life science companies. From 2013 until 2015 he served as Chief Financial Officer of Ruthigen, Inc. From 2005 until 2011, he served as an equity research analyst covering medical devices and diagnostics sectors with Needham & Co, and then subsequently at ThinkEquity. From 2002 through 2005, Mr. Harish worked as a research analyst at Symmetry Capital, a healthcare-focused hedge fund, where he guided investments in the medical device, biotechnology and specialty pharmaceutical companies. Mr. Harish also held research and laboratory positions at Guidant (now part of Abbott Laboratories) and Synteni (acquired by Incyte Corporation). Mr. Harish received a bachelor of arts from the University of California, Berkeley, where he studied molecular and cell biology with an emphasis in immunology.

 

BOARD OF DIRECTORS


 
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Hoji Alimi, Chairman, CEO

Mr. Alimi has over 20 years of experience in the healthcare industry and has raised more than $170 million in capital throughout his career for different ventures. In 1999, he founded Micromed Laboratories Inc. to assist drug and device companies to navigate FDA and European Conformity (“CE”) mark approval processes. In 2002, Mr. Alimi founded Oculus Innovative Sciences, Inc., a company focused on topical anti- infective drugs as well as device-related applications. As CEO and Chairman, he led the company to successfully complete a randomized, double-blind, controlled phase II trial for improvement or cure of infection in diabetic ulcers.  Under his tenure, the company became publicly traded on Nasdaq and achieved dozens of regulatory approvals, including CE marks and 510(K) FDA clearances. In 2012, he founded Ruthigen, Inc. to focus on the development of a drug compound for the reduction of hospital acquired infections during invasive abdominal procedures. As CEO, Chairman and CSO, Ruthigen, Inc. completed an initial public offering and traded on NASDAQ, and later merged with Pulmatrix, a pulmonary-focused pharmaceutical company. Hoji Alimi holds more than 30 patents in areas of anti-infective, surgical, wound care and manufacturing of specific drugs and devices.   He received his B.A. in Biology - Sonoma State University 1995


 
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William H. Watson, III, Vice-President of Business Development

William Watson’s career stems from over 30 years in finance and has grown to provide pivotal business development strategy and implementation for Collidion, Inc. Mr. Watson has been a registered representative and registered principal with FINRA since the early 1980’s. From 2003 to 2007, he joined Brookstreet Securities as the Vice President of Corporate Finance, where he completed 21 engagements totaling over $250 million of private placements, PIPE transactions, initial public offerings, and secondary offerings for small capitalization growth companies.  He has completed an additional $100 million of financing in his career for a variety of other ventures. In addition to financing activities, he also assisted in the assembly of Collidion’s scientific advisory board, interfaced with the board of directors and management, and generated key business development leads with healthcare partners. Since 2013, Mr. Watson has served on the Board of Directors of the National Investment Bankers Association.

 

SCIENTIFIC ADVISORY BOARD


 
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Nicholas DP Cosford, PhD

Dr. Cosford is Professor at Sanford Burnham Medical Research Institute, La Jolla, California. His research is involved in investigating the interactions of small molecule compounds with therapeutically important proteins and cellular signaling pathways. One aspect of his research emphasizes the use of medicinal chemistry and chemical biology approaches to probe intracellular pathways that regulate cell survival and cell growth. Another area of active research is the development of synthetic chemistry methodology using microfluidic technology for the rapid synthesis of biologically active small molecules. Therapeutically, his group is primarily focused on the discovery and optimization of compounds that have the potential to treat cancer, CNS diseases and infectious diseases. He has more than 20 years of experience leading small-molecule drug discovery projects in the pharmaceutical industry. At Sibia Neurosciences and at Merck Research Laboratories he directed multidisciplinary research teams focused on small- molecule hit-to-lead optimization and was responsible for moving several lead compounds through to the clinical phase. Examples include taking a nicotinic receptor agonist (Altinicline, SIB-1508Y) from initiation of research through to Phase II clinical for PD; taking mGluR5 negative allosteric modulators from HTS hits through in vivo proof-of-concept to Phase I clinical (ongoing); and design, synthesis and optimization of an mGluR5 PET tracer clinical candidate; design, synthesis and optimization of an Akt allosteric inhibitor preclinical candidate. To date, he has published more than 55 peer reviewed scientific publications, has more than 30 issued patents, and more than 30 additional patent applications pending. In 2006 he received the FRAXA Research Foundation Award for Outstanding Contributions to Fragile X Research.

 

 

Plex Pharmaceuticals, INC.  – Financial Conflict of Interest Disclosure Form Policy, August, 2017

Objective research is of utmost importance to Plex Pharmaceuticals, Inc. (Plex Pharma), and our sub-awardees and vendors with whom Plex conducts business, to ensure public trust and meet scientific, program and ethical goals of our National Institutes Health (NIH) grant efforts. To address the increasing complexities related to financial interests held by biomedical and behavioral researchers, the Public Health Service (PHS) and the Office of the Secretary of the U.S. Department of Health and Human Services (HHS) has published their final rules. Plex Pharma believes we have fully addressed the requirements (including those of our defined sub-level vendors) of this ruling although we will continue to update this policy as needed, particularly related to any changes in personnel FCOI issues or upon further DHHS guidance.

Effective August 10th, 2017, Plex Pharma’s policy requires that each investigator, subrecipients, subawardees and collaborators affiliated with Plex Pharma, by NIH or any other applicable grant or contract, be in compliance with 42 CFR Part 50, Subpart F for PHS grants and cooperative agreements (and 45 CFR Part 94 for contracts). In addition, this legislation spells out NIH’s commitment to preserving the public’s trust that the research supported by them is conducted without bias and with the highest scientific and ethical standards. Plex Pharma intends to use this same FCOI standard for all other Federal agency grant and contract efforts, as tailored or amended accordingly.

The following are key term definitions and Plex Pharma’s policy guidance for principal or program investigators, subrecipients, subgrantees and collaborators affiliated with Plex Pharma. This policy and all FCOI Plex Pharma guidance are also available at https://www.Plex Pharma.com/fcoipolicy/ (or this document, the Financial Conflict of Interest (FCOI) Policy, to Plex Pharma’s Employee Handbook) so that all interested parties, including the general public have access to this Company policy.

Investigator

An Investigator is any person (including subrecipients, subgrantees and collaborators) who is responsible for the design, conduct or reporting of research funded by PHS.

Training Requirement

Plex Pharma and all defined sub-level vendors are required to complete training related to Financial Conflict of Interest (FCOI). If any conflicts of interest are found or known, they must be disclosed. The training must be updated no-less than every four years or as designated based on grant or role circumstances. Information and other resources developed by NIH will be updated as appropriate and can be accessed through the NIH Web site. (http://grants.nih.gov/grants/policy/coi/tutorial2011/fcoi.htm).

Significant Financial Interest (SFI)

Significant Financial Interest is defined by the regulations as:

  1. A financial interest consisting of one or more of the following interests of the investigator (and those of the investigator’s spouse and dependent children) that reasonable appears to be related to the Investigators institutional responsibilities:

    • With regard to any publically traded entity a significant financial interest exists if the value of any remuneration received from the entity in the twelve months preceding the disclosure and the value of any equity interest in the entity as of the date of disclosure, when aggregated exceeds $5,000. For the purposes of this definition, remuneration includes salary and any payment for services not otherwise identified as salary (e.g. consulting fees, honoraria, paid authorship); equity interest in stock, stock options or other ownership interest, as determined through reference to public prices and other reasonable measures of fair market value;

    • With regard to any non-publicly traded entity, a significant financial interest exists if the value of any remunerations from the entity in the twelve months preceding the disclosure, when aggregated, exceeds $5,000, or when the Investigator (or the Investigator’s spouse or dependent children) holds any equity interests (e.g. stock, stock options, or other ownership interest) or

    • Intellectual property rights and interests (e.g. patents, copyrights), upon receipt of income related to such rights and interests.

  2. Investigators also must disclose the occurrence of any reimbursed or sponsored travel (i.e., that which is paid on behalf of the Investigator and not reimbursed to the Investigator so that the exact monetary value may not be readily available) related to their institutional responsibilities; provided, however, that this disclosure requirement does not apply to travel that is reimbursed or sponsored by a federal , state or local government agency, an institution of higher education as defined at 20 U.S.C. 1001(a), an academic teaching hospital, medical center, or research institute that is affiliated with an Institution of higher education. The Institution’s FCOI policy will specify the details of this disclosure, which will include, at a minimum, the purpose of the trip, the identity of the sponsor/organizer, the destination, and the duration. In accordance with the Institution’s FCOI policy, the institutional official(s) will determine if further information is needed, including a determination or disclosure of monetary value, in order to determine whether the travel constitutes a FCOI with the PHS-funded research.

 

  1. The term significant financial interest does not include the following types of financial interests: salaries, royalties or other remuneration paid by the institution to the Investigator if the Investigator is currently employed or otherwise appointed by the Institution, including intellectual property rights assigned to the Institution and agreements to share in royalties related to such rights; any ownership interest in the Institution held by the investigator, if the Institution is a commercial or for profit organization; income from investment vehicles, such as mutual funds and retirements accounts, as long as the Investigator does not directly control the investment decisions made in these vehicles; income from seminars, lectures or teaching engagements sponsored by a federal , state or local government agency an Institution of higher education as defined at 20 U.S.C. 1001(a), an academic teaching hospital, a medical center, research institute that is affiliated with an Institution of higher education; or income from service on advisory committees or review panels for a federal, state or local government agency an Institution of higher education as defined at 20 U.S.C. 1001(a), an academic teaching hospital, a medical center, or a research institute that is affiliated with an Institution of higher education.

Financial Conflict of Interest (FCOI)

A Financial conflict of interest exists when Plex Pharma reasonably determines that a Significant Financial Interest (defined above) could directly and significantly affect the design, conduct or reporting of NIH-funded research.

Management of a FCOI

Means taking action to address a FCOI, which can include reducing or eliminating the FCOI, to ensure, to the extent possible, that the design, conduct, and reporting of research will be free from bias.

PHS Awarding Component

The PHS awarding component is any sub-agency of the Public Health Service or Department of Health and Human Services.

Records Management

The records of all financial disclosures and all actions taken by Plex Pharma will be maintained for at least three years from the date of submission of the final expenditures report.

Research

PHS research is any project governed by PHS regulation, but excluding applications for Phase I support under the Small Business Innovation Research (SBIR) and Small Business Technology Transfer (STTR) programs

Disclosures/Reporting Process

Plex Pharma ‘s designated official(s) will review all “disclosure” and evaluate whether they contain any FCOI. If no FCOI is found the “disclosure forms” will be filed in the SFI binder. If a FCOI  is identified it will be put on the FCOI report through the eRA Commons FCOI module prior to expending any funds. If any interests are identified as conflicting subsequent to the initial report they must be reported to Plex Pharma within 30 days. Plex Pharma will then report it to the PHS awarding component that has issued the award within 60 days. Each investigator must submit an updated disclosure of an SFI not less than annually. If a PHS-funded project is conducted by an investigator or SO with a conflict that was not disclosed or managed, Plex Pharma is required to disclose the conflict in each public presentation related to the results of the research.

Compliance and Penalties for Non-Performance

If an investigator fails to comply with Plex Pharma’s FCOI policy, within 120 days, Plex Pharma shall complete a retrospective review of the Investigator’s activities to determine bias. If a bias is found, Plex Pharma shall submit a mitigation report to the NIH, in accordance with 42 CFR 50.605(b)(3), that shall address the impact of the bias on the research project and the actions it has taken to mitigate the bias. Plex Pharma will work with the Investigator to set up an FCOI management plan to mitigate the situation. Companywide, Plex Pharma is required to mandate the Investigator disclose the FCOI in each public presentation with research results if it was not reported up front. In extreme cases of bias, the Investigator may lose the right to work on the project or receive any future NIH funding.

Point of Contact

If you have a conflict of interest or if you have a question to discuss, contact the Plex Pharma Signing Official,

Hoji Alimi
(halimi@plexpharma.com)