Seattle Genetics eyes third ADC approval

21 September 2020
esmo_2019_big

A late-breaking paper discussed at the annual congress of ESMO 2020 shows positive data for an investigational antibody-drug conjugate (ADC) developed by Seattle Genetics (Nasdaq: SGEN) and Genmab (Nasdaq: GMAB).

The firms have been testing tisotumab vedotin as monotherapy in people with recurrent and/or metastatic cervical cancer, in the second-line setting.

Presented during a presidential symposium at the annual congress of the European Society for Medical Oncology  (ESMO), the results show a 24% objective response rate (ORR) with a median duration of response (DOR) of 8.3 months.

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 account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
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

Today's issue

Company Spotlight





More Features in Biotechnology