Senhwa Biosciences Inc (TPEx: 6492), a Taiwan-based clinical-stage biopharmaceutical company, announced on Thursday that it has signed a clinical supply agreement with BeOne Medicines, a US-based global oncology company.
This agreement covers a global, multi-centre Phase 1b/2a clinical trial to assess Senhwa's lead compound Pidnarulex (CX-5461) in combination with BeOne's tislelizumab, a PD-1 inhibitor, in patients with advanced solid tumours, including pancreatic ductal adenocarcinoma (PDAC) and immune checkpoint inhibitor (ICI)-refractory melanoma.
BeOne Medicines will supply tislelizumab for the combination study, while Senhwa will provide CX-5461 and lead clinical and regulatory operations. The study will enrol patients at multiple sites in the United States and Taiwan, evaluating safety, tolerability, and preliminary efficacy of the CX-5461 and tislelizumab combination.
CX-5461 was discovered and developed by Senhwa Biosciences Inc. Recent preclinical and clinical findings suggest that CX-5461 not only exerts direct cytotoxic activity but also modulates the tumour microenvironment, enhancing immune recognition and response.
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA