Sobi and ADC Therapeutics Zynlonta (loncastuximab tesirine) Receives EC’s Conditional Marketing Authorisation for Diffuse Large B-Cell Lymphoma
Shots:
- The EC has granted conditional marketing authorization to Zynlonta for the treatment of r/r DLBCL
- The approval was based on data from the P-II trial (LOTIS-2) evaluating Zynlonta in 145 adult patients with r/r DLBCL, following two or more prior lines of systemic therapy. The results showed an ORR of (48.3%) incl. CR rate of 24.1% and a PR rate of 24.1%, patients had a median time to response of 1.3mos. and m-DoR for the 70 responders was 10.3mos.
- The EC’s decision will be valid in all EU member states, Iceland, Norway & Liechtenstein. Sobi & ADC Therapeutics collaborated to develop and commercialize Zynlonta for use in haematology and other indications in the EU and most international markets
Ref: Prnewswire | Image: ADC Therapeutics
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