Year
DEALS // DEV.
Country
Therapeutic Area
Study Phase
Deal Type
Product Type
Dosage Form
Lead Product
Target
Lead Product(s) : Fosdenopterin,Lonafarnib
Therapeutic Area : Genetic Disease
Study Phase : Approved FDF
Recipient : Erkim
Deal Size : Undisclosed
Deal Type : Agreement
Er-Kim, Sentynl Therapeutics Partner on Nulibry® and Zokinvy® for Ultra-Rare Diseases
Details : The agreement aims to Commercialization of Nulibry (fosdenopterin), targeting phosphoro-derivatives for Molybdenum cofactor deficiency Type A.
Product Name : Nulibry
Product Type : Miscellaneous
Upfront Cash : Undisclosed
September 24, 2025
Lead Product(s) : Fosdenopterin,Lonafarnib
Therapeutic Area : Genetic Disease
Highest Development Status : Approved FDF
Recipient : Erkim
Deal Size : Undisclosed
Deal Type : Agreement
Lead Product(s) : Copper Histidine
Therapeutic Area : Rare Diseases and Disorders
Study Phase : Phase III
Sponsor : Fortress Biotech
Deal Size : Inapplicable
Deal Type : Inapplicable
Sentynl Therapeutics Announces FDA Acceptance of CUTX-101 for Menkes Disease
Details : CUTX-101 is a subcutaneous injectable formulation of copper histidinate, which is being evaluated for the treatment of menkes disease.
Product Name : Undisclosed
Product Type : Vitamins/Minerals/Inorganic Salts
Upfront Cash : Inapplicable
January 06, 2025
Lead Product(s) : Copper Histidine
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Phase III
Sponsor : Fortress Biotech
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Lonafarnib
Therapeutic Area : Genetic Disease
Study Phase : Approved FDF
Recipient : Eiger BioPharmaceuticals
Deal Size : Undisclosed
Deal Type : Acquisition
Sentynl Acquires Zokinvy® for Hutchinson-Gilford Progeria Syndrome
Details : Sentynl will commercialize Zokinvy (lonafarnib) globally, the first FDA-approved treatment targeting progeria symptoms.
Product Name : Zokinvy
Product Type : Miscellaneous
Upfront Cash : Undisclosed
May 03, 2024
Lead Product(s) : Lonafarnib
Therapeutic Area : Genetic Disease
Highest Development Status : Approved FDF
Recipient : Eiger BioPharmaceuticals
Deal Size : Undisclosed
Deal Type : Acquisition
Lead Product(s) : Fosdenopterin
Therapeutic Area : Rare Diseases and Disorders
Study Phase : Approved FDF
Sponsor : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Sentynl Receives MHRA Authorization for NULIBRY® in MoCD Type A
Details : Nulibry (fosdenopterin) is the first therapy for patients in Great Britain with molybdenum cofactor deficiency Type A, an ultra-rare genetic disorder that often progresses rapidly in infants.
Product Name : Nulibry
Product Type : Miscellaneous
Upfront Cash : Inapplicable
April 16, 2024
Lead Product(s) : Fosdenopterin
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Approved FDF
Sponsor : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Copper Histidine
Therapeutic Area : Rare Diseases and Disorders
Study Phase : Phase III
Recipient : Cyprium Therapeutics
Deal Size : $133.5 million
Deal Type : Agreement
Details : Under the agreement, Cyprium completed the transfer of its proprietary rights and assigned its FDA documents pertaining to CUTX-101 (copper histidinate) product candidate for the treatment of Menkes disease, to Sentynl.
Product Name : Undisclosed
Product Type : Vitamins/Minerals/Inorganic Salts
Upfront Cash : Undisclosed
December 06, 2023
Lead Product(s) : Copper Histidine
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Phase III
Recipient : Cyprium Therapeutics
Deal Size : $133.5 million
Deal Type : Agreement
Lead Product(s) : Fosdenopterin
Therapeutic Area : Genetic Disease
Study Phase : Approved FDF
Recipient : BridgeBio Pharma
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : Nulibry (fosdenopterin) is a first-in-class cPMP substrate replacement therapy that was approved by the U.S. Food and Drug Administration (FDA) in 2021 to reduce the risk of mortality in patients with MoCD Type A.
Product Name : Nulibry
Product Type : Miscellaneous
Upfront Cash : Inapplicable
September 20, 2022
Lead Product(s) : Fosdenopterin
Therapeutic Area : Genetic Disease
Highest Development Status : Approved FDF
Recipient : BridgeBio Pharma
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Fosdenopterin
Therapeutic Area : Genetic Disease
Study Phase : Approved FDF
Recipient : BridgeBio Pharma
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : NULIBRY (fosdenopterin) is first and only approved therapy in U.S. and in Israel to treat patients with MoCD Type A, an ultra-rare, life-threatening genetic disorder that often progresses rapidly in infants with a median overall survival age of about fou...
Product Name : Nulibry
Product Type : Miscellaneous
Upfront Cash : Inapplicable
August 10, 2022
Lead Product(s) : Fosdenopterin
Therapeutic Area : Genetic Disease
Highest Development Status : Approved FDF
Recipient : BridgeBio Pharma
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Fosdenopterin
Therapeutic Area : Genetic Disease
Study Phase : Approved FDF
Recipient : BridgeBio Pharma
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : CHMP recommendation for approval of NULIBRY (fosdenopterin) in European Union (EU) for the treatment of patients with molybdenum cofactor deficiency (MoCD) Type A is based on the efficacy and safety data collected to date compared to data from a natural ...
Product Name : Nulibry
Product Type : Miscellaneous
Upfront Cash : Inapplicable
July 25, 2022
Lead Product(s) : Fosdenopterin
Therapeutic Area : Genetic Disease
Highest Development Status : Approved FDF
Recipient : BridgeBio Pharma
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Fosdenopterin
Therapeutic Area : Genetic Disease
Study Phase : Approved FDF
Recipient : BridgeBio Pharma
Deal Size : Undisclosed
Deal Type : Agreement
Details : Under the Agreement, Sentynl will acquire global rights to NULIBRY and will be responsible for the ongoing development and commercialization of NULIBRY in the United States and developing, manufacturing and commercializing Fosdenopterin globally.
Product Name : Nulibry
Product Type : Miscellaneous
Upfront Cash : Undisclosed
March 08, 2022
Lead Product(s) : Fosdenopterin
Therapeutic Area : Genetic Disease
Highest Development Status : Approved FDF
Recipient : BridgeBio Pharma
Deal Size : Undisclosed
Deal Type : Agreement
Lead Product(s) : Copper Histidine
Therapeutic Area : Rare Diseases and Disorders
Study Phase : Phase III
Recipient : Cyprium Therapeutics
Deal Size : Undisclosed
Deal Type : Acquisition
Cyprium Therapeutics and Sentynl Therapeutics Sign Development and Asset Purchase Agreement
Details : Sentynl has signed an agreement with Cyprium to contribute research funding for CUTX-101, a Copper Histidinate product candidate for the treatment of Menkes disease, and to purchase Cyprium's proprietary rights to CUTX-101.
Product Name : Undisclosed
Product Type : Vitamins/Minerals/Inorganic Salts
Upfront Cash : $20.0 million
February 24, 2021
Lead Product(s) : Copper Histidine
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Phase III
Recipient : Cyprium Therapeutics
Deal Size : Undisclosed
Deal Type : Acquisition