EC approves Tepkinly combination for relapsed follicular lymphoma

7 July 2026

The European Commission has approved Danish biotech Genmab (Nasdaq Copenhagen: GMAB) and US pharma major AbbVie’s (NYSE: ABBV) Tepkinly (epcoritamab) in combination with lenalidomide and rituximab for adults with relapsed or refractory follicular lymphoma, widening the bispecific antibody’s European label into an earlier treatment setting.

This regimen is the first bispecific-based therapy approved in Europe for follicular lymphoma in the second-line setting.

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