China-based biotech Duality Biologic (DualityBio) announced first data from a global Phase I/IIa clinical trial evaluating BNT324/DB-1311, an investigational next-generation antibody-drug conjugate (ADC) targeting the transmembrane glycoprotein B7-H3.
The data were presented in an oral session at the 2024 European Society of Medical Oncology Asia Annual Meeting (ESMO Asia) in Singapore and showed encouraging antitumor activity alongside a manageable safety profile in heavily pre-treated patients with locally advanced or metastatic solid tumors.
BNT324/DB-1311 is being co-developed by Germany’s BioNTech (Nasdaq: BNTX) and DualityBio under a deal signed last year under which the Chinese firm earned an upfront of $170 million and became eligible for up to $1.5 billion in milestones.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze