Genmab’s TEPKINLY Gains EU Approval for Lymphoma
Company Announcements

Genmab’s TEPKINLY Gains EU Approval for Lymphoma

Genmab (GMAB) has released an update.

Genmab A/S has announced the European Commission’s approval of TEPKINLY (epcoritamab) as a groundbreaking monotherapy for adults with relapsed or refractory follicular lymphoma, after two or more systemic therapies. This marks TEPKINLY as the first and only subcutaneous bispecific antibody authorized in the EU for this condition. The approval is supported by promising results from the EPCORE NHL-1 clinical trial showing high response rates in patients with limited treatment options.

For further insights into GMAB stock, check out TipRanks’ Stock Analysis page.

Related Articles
TheFlyGenmab launches partnership with OpenAI for ‘AI Everywhere’
TheFlyGenmab announces new data from Phase 1/2 study of Rina-S
GlobeNewswireInvestigational Rinatabart Sesutecan (Rina-S) Shows Promising Anti-Tumor Activity as Single Agent in Heavily Pretreated Patients with Ovarian and Endometrial Cancers in Phase 1/2 Clinical Trial
Looking for investment ideas? Subscribe to our Smart Investor newsletter for weekly expert stock picks!
Get real-time notifications on news & analysis, curated for your stock watchlist. Download the TipRanks app today! Get the App