
Shares in Switzerland-based ADC Therapeutics (NYSE: ADCT) fell sharply in pre-market trading on Thursday after investors focused on safety findings and the lack of a clear overall survival advantage in the Phase III LOTIS-5 trial of Zynlonta (loncastuximab tesirine-lpyl) plus rituximab in relapsed or refractory diffuse large B-cell lymphoma (DLBCL).
The company said the study met its primary endpoint, with Zynlonta plus rituximab significantly improving progression-free survival (PFS) compared with rituximab plus gemcitabine and oxaliplatin. Median PFS was 6.1 months versus 4.7 months, with a hazard ratio of 0.73.
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
| Headless Content Management with Blaze