Histogen Announces Investigational Device Exemption Application for HST 002
CONATUS PHARMACEUTICALS INC (CNAT)
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Source: GlobeNewswire
SAN DIEGO, April 20, 2020 (GLOBE NEWSWIRE) -- Histogen Inc., a regenerative medicine company with a novel biological platform that replaces and regenerates tissues in the body, announced today that it has submitted an Investigational Device Exemption (IDE) application with the U.S. Food and Drug Administration (FDA) for the initiation of a Phase 1 clinical trial of HST 002 for the treatment of facial folds and wrinkles. HST 002 is a naturally produced collagen and extracellular matrix dermal filler targeting the treatment of facial folds and wrinkles. The planned Phase 1 clinical trial is designed to assess the safety and tolerability of HST 002, as well as look for early indications of efficacy versus a placebo control. “The submission of this Investigational Device Exemption for HST 002 is an important milestone for Histogen as we continue to advance our development pipeline following the recent submission of our Investigational New Drug Application Amendment for HST 001 for hai
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