Year
DEALS // DEV.
Country
Therapeutic Area
Study Phase
Deal Type
Product Type
Dosage Form
Lead Product
Target
Lead Product(s) : Tunlametinib
Therapeutic Area : Oncology
Study Phase : Approved
Sponsor : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
KeChow Gets NMPA Approval for Tunlametinib as First Targeted Therapy for NRAS Melanoma
Details : HL-085 (tunlametinib) is a small molecule inhibitor of Mitogen-activated protein kinase. It is approved by NMPA for the treatment of NRAS Mutated Advanced Melanoma.
Brand Name : HL-085
Molecule Type : Small molecule
Upfront Cash : Not Applicable
March 18, 2024
Lead Product(s) : Tunlametinib
Therapeutic Area : Oncology
Highest Development Status : Approved
Sponsor : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Lead Product(s) : Vemurafenib
Therapeutic Area : Oncology
Study Phase : Approved
Sponsor : F. Hoffmann-La Roche
Deal Size : Undisclosed
Deal Type : Collaboration
Roche and KeChow Reach a Cooperation Agreement
Details : Under this collaboration, KeChow will promote Roche's Zelboraf® in China. Zelboraf® is an oral small molecule, selective BRAF inhibitor indicated for the treatment of patients with BRAF V600 mutation-positive advanced or inoperable melanoma.
Brand Name : Zelboraf
Molecule Type : Small molecule
Upfront Cash : Undisclosed
August 20, 2021
Lead Product(s) : Vemurafenib
Therapeutic Area : Oncology
Highest Development Status : Approved
Sponsor : F. Hoffmann-La Roche
Deal Size : Undisclosed
Deal Type : Collaboration
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