Lead Product(s) : CAS 492-27-3
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Study Phase : Phase II/ Phase III
Sponsor : Nutrasource
Deal Size : Inapplicable
Deal Type : Inapplicable
Post-Operative Use of FS2 to Mitigate Scarring in Burn Patients
Details : Kynurenic Acid is a Other Small Molecule drug candidate, which is currently being evaluated in phase II/ phase III clinical studies for the treatment of Burn Scar.
Product Name : Undisclosed
Product Type : Miscellaneous
Upfront Cash : Inapplicable
February 04, 2025
Lead Product(s) : CAS 492-27-3
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Highest Development Status : Phase II/ Phase III
Sponsor : Nutrasource
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Human Acellular Vessel
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Study Phase : Phase II/ Phase III
Sponsor : Undisclosed
Deal Size : $15.0 million
Deal Type : Public Offering
Humacyte Announces Pricing of $15.0 Million Registered Direct Offering
Details : The proceeds will fund the development of the product candidates in company's pipeline and the planned commercial launch of the ATEV in the vascular trauma indication.
Product Name : Humacyl
Product Type : Cell & Gene Therapy
Upfront Cash : Undisclosed
November 14, 2024
Lead Product(s) : Human Acellular Vessel
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Highest Development Status : Phase II/ Phase III
Sponsor : Undisclosed
Deal Size : $15.0 million
Deal Type : Public Offering
Lead Product(s) : Human Acellular Vessel
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Study Phase : Phase II/ Phase III
Sponsor : EF Hutton
Deal Size : $30.0 million
Deal Type : Public Offering
Humacyte Announces Pricing of $30.0 Million Registered Direct Offering
Details : The company will use the proceeds to fund the development of the product candidates in its pipeline, including
Product Name : Humacyl
Product Type : Cell & Gene Therapy
Upfront Cash : Undisclosed
October 04, 2024
Lead Product(s) : Human Acellular Vessel
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Highest Development Status : Phase II/ Phase III
Sponsor : EF Hutton
Deal Size : $30.0 million
Deal Type : Public Offering
Lead Product(s) : Dexmedetomidine Hydrochloride
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Study Phase : Phase II/ Phase III
Sponsor : Canadian Critical Care Trials Group
Deal Size : Inapplicable
Deal Type : Inapplicable
Effects of Dexmedetomidine on Agitation in Critically Ill TBI Patients
Details : Dexmedetomidine is a Other Small Molecule drug candidate, which is currently being evaluated in phase II/ phase III clinical studies for the treatment of Brain Injuries, Traumatic.
Product Name : Undisclosed
Product Type : Miscellaneous
Upfront Cash : Inapplicable
October 01, 2024
Lead Product(s) : Dexmedetomidine Hydrochloride
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Highest Development Status : Phase II/ Phase III
Sponsor : Canadian Critical Care Trials Group
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : iCM012
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Study Phase : Phase II/ Phase III
Sponsor : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : ICM012 is a drug candidate, which is currently being evaluated in phase II/ phase III clinical studies for the treatment of Reperfusion Injury.
Product Name : Undisclosed
Product Type : Undisclosed
Upfront Cash : Inapplicable
September 03, 2024
Lead Product(s) : iCM012
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Highest Development Status : Phase II/ Phase III
Sponsor : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Human Acellular Vessel
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Study Phase : Phase II/ Phase III
Sponsor : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Humacyte FDA Review of ATEV™ For Vascular Trauma Requires Extra Time
Details : The company submitted a Biologics License Application (BLA) to the USFDA for its RMAT-designated product, V005 Human Acellular Vessel, meant for the treatment of vascular trauma.
Product Name : Humacyl
Product Type : Cell & Gene Therapy
Upfront Cash : Inapplicable
August 09, 2024
Lead Product(s) : Human Acellular Vessel
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Highest Development Status : Phase II/ Phase III
Sponsor : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : TPX-115
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Study Phase : Phase II/ Phase III
Sponsor : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
A Phase 2b/3 Study of TPX-115 on Partial-thickness Rotator Cuff Tear
Details : TPX-115 is a drug candidate, which is currently being evaluated in phase II/ phase III clinical studies for the treatment of Rotator Cuff Injuries.
Product Name : Undisclosed
Product Type : Undisclosed
Upfront Cash : Inapplicable
May 14, 2024
Lead Product(s) : TPX-115
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Highest Development Status : Phase II/ Phase III
Sponsor : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Human Acellular Vessel
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Study Phase : Phase II/ Phase III
Sponsor : TD Cowen
Deal Size : $40.2 million
Deal Type : Public Offering
Humacyte, Inc. Announces Pricing of $40.2 Million Public Offering of Common Stock
Details : Humacyte intends to use the net proceeds for the clinical development of HAV (human acellular vessel) for the treatment of arterial repair following extremity vascular trauma.
Product Name : Humacyl
Product Type : Cell & Gene Therapy
Upfront Cash : Undisclosed
February 29, 2024
Lead Product(s) : Human Acellular Vessel
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Highest Development Status : Phase II/ Phase III
Sponsor : TD Cowen
Deal Size : $40.2 million
Deal Type : Public Offering
Lead Product(s) : Human Acellular Vessel
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Study Phase : Phase II/ Phase III
Sponsor : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
HAV Biologics License Application Granted Priority Review for Vascular Trauma
Details : HAV is an acellular graft made of human collagen and extracellular matrix proteins, under development for life-threatening vascular trauma.
Product Name : Humacyl
Product Type : Cell & Gene Therapy
Upfront Cash : Inapplicable
February 09, 2024
Lead Product(s) : Human Acellular Vessel
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Highest Development Status : Phase II/ Phase III
Sponsor : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Human Acellular Vessel
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Study Phase : Phase II/ Phase III
Sponsor : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : Company submitted a Biologics License Application (BLA) to USFDA for its RMAT designated product, Human Acellular Vessel, meant for the treatment of vascular trauma.
Product Name : Humacyl
Product Type : Cell & Gene Therapy
Upfront Cash : Inapplicable
December 12, 2023
Lead Product(s) : Human Acellular Vessel
Therapeutic Area : Trauma (Emergency, Injury, Surgery)
Highest Development Status : Phase II/ Phase III
Sponsor : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable