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FDA grants STeP designation for Pear Therapeutics’ neurobehavioral digital therapeutic

April 13, 2022 By Sean Whooley

Pear TherapeuticsPear Therapeutics (Nasdaq:PEAR) announced today that it received STeP designation from the FDA for its Pear-010 product candidate.

Boston-based Pear Therapeutics designed its Pear-010 prescription digital therapeutic (PDT) candidate to provide a neurobehavioral intervention (virtual reality-delivered pain reduction) to patients 18 and older with acute postoperative and acute postprocedural pain.

Get the full story at our sister site, MassDevice.

Filed Under: Drug-Device Combinations, Food & Drug Administration (FDA), Neurological, Regulatory/Compliance, Technology Tagged With: FDA, Pear Therapeutics

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About Sean Whooley

Sean Whooley is an associate editor who mainly produces work for MassDevice, Medical Design & Outsourcing and Drug Delivery Business News. He received a bachelor's degree in multiplatform journalism from the University of Maryland, College Park. You can connect with him on LinkedIn or email him at [email protected].

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