Japan-based Daiichi Sankyo Company Limited and Sarah Cannon Research Institute, a subsidiary of HCA Healthcare, have dosed the first patient in a first-in-human phase 1/2 study assessing DS-7300, an investigational B7-H3 targeting antibody drug conjugate, intended to treat patients with various advanced solid tumours that have progressed on standard treatments or for whom no standard treatment exists, it was reported on Friday.
The study is the first in the strategic oncology collaboration between both firms, intended to accelerate and optimise global clinical development of Daiichi Sankyo's novel antibody drug conjugates and other targeted cancer therapies by merging the operational and scientific expertise of both organisations.
The product is the fourth antibody drug conjugate in clinical development using Daiichi Sankyo's proprietary DXd technology and it was designed to target and deliver chemotherapy inside cancer cells that express the B7-H3 protein, which is frequently overexpressed in various types of cancers and has been associated with disease progression and poor prognosis in many tumour types.
SenderraRx receives reaccreditation in Specialty Pharmacy from ACHC
EMA issues positive CHMP opinion for Revolution Medicines' RASONQUE in metastatic pancreatic cancer
Telix to present 20 abstracts on cancer theranostics at EANM Congress
CelLBxHealth secures USD65,000 pharmaceutical research contract
Racura Oncology receives approval for RC220 trial to proceed to higher dose
Foresee gains NMPA approval for CAMCEVI 42 mg in China
ABL Texcell Diagnostics acquires IntegraGen assets to expand into precision oncology
Akeso reports first patient dosed in Phase III study of cadonilimab in colon cancer
Natera secures FDA Breakthrough Device designation for multi-cancer early detection assay
FDA approves Genentech's Tecentriq combination therapy for stage III colon cancer
Alpheus Medical starts new clinical trial of PoMA therapy in butterfly glioblastoma
Sophos IRB and ALCMI partner to support lung cancer research
Northwest Biotherapeutics and NHSBT collaborate to support production of DCVax-L
Vir Biotechnology's VIR-5500 receives FDA Fast Track designation for prostate cancer