Biotechnology company Cereno Scientific (Nasdaq First North: CRNO B) on Wednesday reported publication of the first peer-reviewed manuscript on its HDAC inhibitor CS014 in the Journal of Thrombosis and Haemostasis, disclosing molecular structure, mechanism of action and nonclinical pharmacology data supporting broad potential in cardiovascular and pulmonary diseases.
The publication demonstrates that CS014 delivers strong antithrombotic effects across small artery, large artery and large vein models at doses that preserve normal haemostasis and bleeding time. Data show maintained HDAC inhibitory activity, increased tissue plasminogen activator mRNA expression and substantially lower formation of the hepatotoxic 4-ene metabolite compared with valproic acid, supporting a differentiated safety profile.
Findings validate HDAC inhibition as a core mechanism underpinning CS014's potential to address interconnected processes of thrombosis, vascular remodelling and fibrosis. Results position CS014 as a next-generation HDAC inhibitor and novel chemical entity with potential application across thrombotic and fibrosis-driven cardiopulmonary conditions.
Cereno Scientific recently reported positive Phase I results confirming favourable safety and tolerability at and above exposure levels predicted to support maximal therapeutic effects based on nonclinical data. The company is preparing for Phase II development with an initial focus on idiopathic pulmonary fibrosis, targeting diseases with high unmet medical need.
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