10
ALL8
Kyowa Kirin2
Ultragenyx PharmaceuticalYear
10
ALL2
20243
20222
20213
2020DEALS // DEV.
10
ALL3
Deals7
DevelopmentsCountry
10
ALL8
JAPAN2
U.S.A10
ALL1
DKSH6
Inapplicable1
Kyowa Kirin1
NewBridge Pharmaceuticals1
Ultragenyx PharmaceuticalTherapeutic Area
10
ALL6
Genetic Disease2
Musculoskeletal2
Rare Diseases and DisordersStudy Phase
10
ALL9
Approved FDF1
Phase IIDeal Type
10
ALL1
Agreement1
Divestment7
Inapplicable1
PartnershipProduct Type
10
ALL10
AntibodyDosage Form
10
ALL10
Subcutaneous InjectionLead Product
10
ALL10
BurosumabTarget
10
ALL10
FGF23Lead Product(s) : Burosumab
Therapeutic Area : Genetic Disease
Study Phase : Approved FDF
Sponsor : DKSH
Deal Size : Undisclosed
Deal Type : Partnership
DKSH and Kyowa Kirin Forge Strategic Partnership Across Asia-Pacific
Details : The partnership covers a promotion and distribution agreement for commercial rights of Kyowa’s established medicines, including Crysvita (burosumab), indicated for X-linked hypophosphatemia.
Product Name : Crysvita
Product Type : Antibody
Upfront Cash : Undisclosed
August 02, 2024
Lead Product(s) : Burosumab
Therapeutic Area : Genetic Disease
Highest Development Status : Approved FDF
Sponsor : DKSH
Deal Size : Undisclosed
Deal Type : Partnership
Lead Product(s) : Burosumab
Therapeutic Area : Rare Diseases and Disorders
Study Phase : Approved FDF
Sponsor : NewBridge Pharmaceuticals
Deal Size : Undisclosed
Deal Type : Agreement
Kyowa Kirin and NewBridge Enter Agreement to Improve Rare Disease Access in MENA
Details : Under the terms of the agreement, NewBridge will commercialise CRYSVITA (burosumab), which is indicated for the treatment of X-Linked Hypophosphataemia.
Product Name : Crysvita
Product Type : Antibody
Upfront Cash : Undisclosed
July 08, 2024
Lead Product(s) : Burosumab
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Approved FDF
Sponsor : NewBridge Pharmaceuticals
Deal Size : Undisclosed
Deal Type : Agreement
Lead Product(s) : Burosumab
Therapeutic Area : Musculoskeletal
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : CRYSVITA (burosumab) is a recombinant fully human monoclonal antibody that binds to and inhibits the activity of FGF23.2 CRYSVITA blocks the action of FGF23, which is produced in excess in TIO, restoring phosphate homeostasis.
Product Name : Crysvita
Product Type : Antibody
Upfront Cash : Inapplicable
August 19, 2022
Lead Product(s) : Burosumab
Therapeutic Area : Musculoskeletal
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Burosumab
Therapeutic Area : Rare Diseases and Disorders
Study Phase : Approved FDF
Sponsor : Kyowa Kirin
Deal Size : $500.0 million
Deal Type : Divestment
Details : Crysvita (burosumab) is a recombinant fully human monoclonal IgG1 antibody, discovered by Kyowa Kirin, against the phosphaturic hormone FGF23. Crysvita is designed to bind to and thereby inhibit the biological activity of FGF23.
Product Name : Crysvita
Product Type : Antibody
Upfront Cash : Undisclosed
July 14, 2022
Lead Product(s) : Burosumab
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Approved FDF
Sponsor : Kyowa Kirin
Deal Size : $500.0 million
Deal Type : Divestment
Lead Product(s) : Burosumab
Therapeutic Area : Genetic Disease
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : CRYSVITA (burosumab) was created and developed by Kyowa Kirin and is a recombinant fully human monoclonal antibody that binds to and inhibits the activity of FGF23.2 CRYSVITA blocks the action of FGF23, restoring phosphate homeostasis.
Product Name : Crysvita
Product Type : Antibody
Upfront Cash : Inapplicable
June 27, 2022
Lead Product(s) : Burosumab
Therapeutic Area : Genetic Disease
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Burosumab
Therapeutic Area : Genetic Disease
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : The Committee indicated that, if a patient is receiving a stable dose of Crysvita (burosumab), their treating physician can then recommend that administration be performed by the patient or their carer following training.
Product Name : Crysvita
Product Type : Antibody
Upfront Cash : Inapplicable
October 05, 2021
Lead Product(s) : Burosumab
Therapeutic Area : Genetic Disease
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Burosumab
Therapeutic Area : Genetic Disease
Study Phase : Approved FDF
Sponsor : Ultragenyx Pharmaceutical
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : Crysvita® (burosumab-twza) is a fibroblast growth factor 23 (FGF23)-blocking antibody indicated for the treatment of X-linked hypophosphatemia and FGF23-related hypophosphatemia.
Product Name : Crysvita
Product Type : Antibody
Upfront Cash : Inapplicable
September 27, 2021
Lead Product(s) : Burosumab
Therapeutic Area : Genetic Disease
Highest Development Status : Approved FDF
Sponsor : Ultragenyx Pharmaceutical
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Burosumab
Therapeutic Area : Genetic Disease
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : The European Commission has already granted a conditional marketing authorisation for CRYSVITA for the treatment of XLH with radiographic evidence of bone disease in children one year of age and older and adolescents with growing skeletons.
Product Name : Crysvita
Product Type : Antibody
Upfront Cash : Inapplicable
July 27, 2020
Lead Product(s) : Burosumab
Therapeutic Area : Genetic Disease
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Burosumab
Therapeutic Area : Genetic Disease
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : CRYSVITA, created by Kyowa Kirin, is a recombinant fully human monoclonal IgG1 antibody against the FGF23. More people in Europe are now eligible for treatment with CRYSVITA, the only therapy that targets the underlying pathophysiology of XLH.
Product Name : Crysvita
Product Type : Antibody
Upfront Cash : Inapplicable
May 10, 2020
Lead Product(s) : Burosumab
Therapeutic Area : Genetic Disease
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Burosumab
Therapeutic Area : Musculoskeletal
Study Phase : Phase II
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : The sBLA package includes data from two single-arm Phase 2 studies including 14 adult patients conducted by Ultragenyx in the U.S. and 13 adult patients conducted by Kyowa Kirin in Japan.
Product Name : Crysvita
Product Type : Antibody
Upfront Cash : Inapplicable
January 14, 2020
Lead Product(s) : Burosumab
Therapeutic Area : Musculoskeletal
Highest Development Status : Phase II
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable