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Pear Therapeutics to Participate in the BTIG Digital Health Forum
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Pear Therapeutics, the leader in prescription digital therapeutics (PDTs), announces participation in the virtual BTIG Digital Health Forum on November 15. CEO Corey McCann will join a panel discussion titled “Setting the Pace: Commercializing Prescription Digital Therapeutics and Expanding the Pipeline” at 2:00 p.m. ET, moderated by Marie Thibault. Pear is known for pioneering FDA-approved PDTs such as reSET, reSET-O, and Somryst. These products aim to redefine treatment approaches in various therapeutic areas, enhancing patient outcomes and clinician engagement.
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BOSTON--(BUSINESS WIRE)--
Pear Therapeutics, Inc., the leader in developing and commercializing prescription digital therapeutics (PDTs) to treat serious disease, today announced management’s participation in the virtual BTIG Digital Health Forum being held on Monday, November 15.
Corey McCann, M.D., Ph.D., President and CEO, will participate in a panel discussion at 2:00 p.m. ET. The panel, “Setting the Pace: Commercializing Prescription Digital Therapeutics (PDTs) and Expanding the Pipeline,” will be moderated by Marie Thibault, BTIG Medical Technology and Digital Health Analyst.
BTIG hosted events are intended for prospective and existing BTIG clients only. To listen to the live event, please contact your BTIG representative with interest.
About Pear Therapeutics
Pear Therapeutics is the leader in prescription digital therapeutics, or PDTs. Pear aims to redefine medicine by discovering, developing, and delivering clinically validated software-based therapeutics to provide better outcomes for patients, smarter engagement and tracking tools for clinicians, and cost-effective solutions for payers. Pear has a pipeline of products and product candidates across therapeutic areas, including the first three PDTs with disease treatment claims from FDA. Pear’s lead product, reSET®, for the treatment of substance use disorder, was the first PDT to receive marketing authorization from FDA to treat disease. Pear’s second product, reSET-O®, for the treatment of opioid use disorder, was the first PDT to receive Breakthrough Designation. Pear’s third product, Somryst®, for the treatment of chronic insomnia, was the first PDT submitted through FDA’s traditional 510(k) pathway while simultaneously reviewed through FDA’s Software Precertification Pilot Program. For more information, visit Pear at www.peartherapeutics.com.
