Year
DEALS // DEV.
Country
Therapeutic Area
Study Phase
Deal Type
Product Type
Dosage Form
Lead Product
Target
Lead Product(s) : CLS001
Therapeutic Area : Ophthalmology
Study Phase : IND Enabling
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Cellusion Receives U.S. FDA Orphan Drug Designation for CLS001
Details : U.S. FDA has granted Orphan Drug Designation for Cellusion CLS001, a therapeutic regenerative medicine product. It is currently undergoing IND Enabling studies for the treatment of bullous keratopathy.
Product Name : CLS001
Product Type : Cell and Gene therapy
Upfront Cash : Inapplicable
December 22, 2023
Lead Product(s) : CLS001
Therapeutic Area : Ophthalmology
Highest Development Status : IND Enabling
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : CLS001
Therapeutic Area : Ophthalmology
Study Phase : Preclinical
Sponsor : Hangzhou Celregen Therapeutics
Deal Size : $100.0 million
Deal Type : Licensing Agreement
Details : Under the Agreement, Celregen will have the exclusive right to develop, manufacture and commercialize CLS001 for bullous keratopathy in the Greater China region, including Mainland China, Hong Kong, Macau and Taiwan.
Product Name : CLS001
Product Type : Cell and Gene therapy
Upfront Cash : Undisclosed
December 09, 2022
Lead Product(s) : CLS001
Therapeutic Area : Ophthalmology
Highest Development Status : Preclinical
Sponsor : Hangzhou Celregen Therapeutics
Deal Size : $100.0 million
Deal Type : Licensing Agreement