Cyclo Therapeutics Appoints Lori McKenna Gorski as Global Head of Patient Advocacy
Cyclo Therapeutics, Inc. (Nasdaq: CYTH) announced the appointment of Lori McKenna Gorski as Global Head of Patient Advocacy. Gorski, with over 20 years of experience in biotechnology and rare disease advocacy, aims to enhance support for patients with Niemann-Pick Disease Type C1. The Company’s lead program, Trappsol® Cyclo™, is undergoing pivotal studies and aims to address significant unmet patient needs. Gorski's commitment aligns with Cyclo's mission to deliver patient-focused therapies, leveraging her expertise from Sanofi Genzyme and her consultancy work.
- Appointment of Lori Gorski as Global Head of Patient Advocacy brings extensive experience in rare disease advocacy.
- Gorski's leadership may enhance patient engagement and support for Niemann-Pick Disease Type C1.
- Trappsol® Cyclo™ is advancing towards pivotal studies, addressing urgent patient needs.
- None.
Cyclo Therapeutics, Inc. (Nasdaq: CYTH) (“Cyclo Therapeutics” or the “Company”), a clinical stage biotechnology company dedicated to developing life-changing medicines through science and innovation for patients and families suffering from diseases, announced today it has appointed Lori McKenna Gorski as Global Head of Patient Advocacy.
“The unmet needs of patients and their families remain at the forefront for Cyclo Therapeutics as we drive the development of our lead program, Trappsol® Cyclo™, towards our pivotal study in the treatment of Niemann-Pick Disease Type C1. Lori’s passion and commitment to helping patients with rare diseases, along with her specific experience with lysosomal storage disorders from her tenure at Sanofi Genzyme, are perfectly aligned with our vision to provide hope through patient-focused drug development to improve quality of life. She brings a wealth of relevant experience and we are thrilled to have Lori join the Cyclo Therapeutics family to lead our patient advocacy initiatives globally,” said N. Scott Fine, Chief Executive Officer of Cyclo Therapeutics.
Ms. Gorski added, “While there has been progress, there remains tremendous unmet need for those living with Niemann-Pick Disease, and I am honored to learn and help support this rare and resilient community. Our collective commitment at Cyclo Therapeutics is to work aggressively to advance our lead program, while we partner with the NPC patient community to better understand their journeys, support their patient advocacy goals and work together to improve the lives of patients and families in need.”
Ms. Gorski is a well-established biotechnology executive with over 20 years of experience specializing in patient advocacy for rare disease communities, including supporting clinical trial and access strategies, patient engagement and disease awareness communications. In 2017, Ms. Gorski founded a consultancy business to advise biotechnology companies in the U.S. and Europe on patient advocacy and communications strategies, working to support innovation and access to therapies that can address unmet medical needs and transform lives. She also spent several years at Sanofi Genzyme where she led global communications for rare diseases, including lysosomal storage disorders, for their clinical development programs, patient advocacy programs and disease awareness initiatives. She later joined Sanofi Genzyme’s Global Patient Advocacy team where she initiated programs to support disease awareness, provide caregiver support and communicate clinical program updates. She began her career at the global public relations agency Brodeur Worldwide and eventually moved to an in-house role at Thermo Fisher Scientific, where she oversaw communications activities for 12 divisions worldwide, financial media relations, and executive communications. Additionally, she currently serves as a board member of Our Odyssey, an organization dedicated to connecting young adults impacted by a rare or chronic condition with social and emotional support in the hope of improving our quality of life.
About Cyclo Therapeutics
Cyclo Therapeutics, Inc. is a clinical-stage biotechnology company dedicated to developing life-changing medicines through science and innovation for patients and families suffering from disease. The Company’s Trappsol® Cyclo™, an orphan drug designated product in the United States and Europe, is the subject of three ongoing formal clinical trials for Niemann-Pick Disease Type C, a rare and fatal genetic disease, (www.ClinicalTrials.gov NCT02939547, NCT02912793, NCT03893071 and NCT04860960). The Company is planning an early phase clinical trial using Trappsol® Cyclo™ intravenously in Alzheimer’s Disease based on encouraging data from an Expanded Access program for late-onset Alzheimer’s Disease (NCT03624842). Additional indications for the active ingredient in Trappsol® Cyclo™ are in development. For additional information, visit the Company’s website: www.cyclotherapeutics.com.
Safe Harbor Statement
This press release contains “forward-looking statements” about the company’s current expectations about future results, performance, prospects and opportunities, including, without limitation, statements regarding the satisfaction of closing conditions relating to the offering and the anticipated use of proceeds from the offering. Statements that are not historical facts, such as “anticipates,” “believes” and “expects” or similar expressions, are forward-looking statements. These statements are subject to a number of risks, uncertainties and other factors that could cause actual results in future periods to differ materially from what is expressed in, or implied by, these statements. The factors which may influence the company’s future performance include the company’s ability to obtain additional capital to expand operations as planned, success in achieving regulatory approval for clinical protocols, enrollment of adequate numbers of patients in clinical trials, unforeseen difficulties in showing efficacy of the company’s biopharmaceutical products, success in attracting additional customers and profitable contracts, and regulatory risks associated with producing pharmaceutical grade and food products. These and other risk factors are described from time to time in the company’s filings with the Securities and Exchange Commission, including, but not limited to, the company’s reports on Forms 10-K and 10-Q. Unless required by law, the company assumes no obligation to update or revise any forward-looking statements as a result of new information or future events.
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