AsymBio, a China-based global Contract Development and Manufacturing Organisation (CDMO) and a subsidiary of Asymchem Group (SZ:002821, HK:6821), announced on Monday that it has commenced commercial production at its Shanghai Fengxian Commercial Manufacturing Base.
This expands AsymBio's integrated, end-to-end biologics CDMO services.
Coving 130,000 square metres, the Fengxian facility is designed to provide flexible, scalable support across all clinical phases, enabling tailored CDMO solutions from early development through commercial production. It will produce an expanded range of next-generation biotherapeutics, including ADCs, dual-payload ADCs, RDCs, APCs, PDCs, AOCs, and monoclonal, bispecific, and multi-specific antibodies and recombinant proteins.
Phase IA is dedicated to antibody manufacturing, featuring single-use bioreactors (200L, 500L, and 2000L) with a total drug substance capacity of 66,000 litres. A 20-square-metre lyophiliser supports production of up to one million vials of lyophilised antibody drug product annually.
Phase IB is focused on bioconjugate manufacturing, equipped with 200L and 500L reactors for all clinical phases. The drug product area includes clinical-scale lines (10-square-metre and 15-square-metre lyophilisers) and commercial-scale lines (two 20-square-metre lyophilisers), enabling annual output of up to two million vials.
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