Prognia
Drug Database
🇪🇺EU · EMAWithdrawnATC: L01EM04

Copiktra(duvelisib)

Leukemia, Lymphocytic, Chronic, B-Cell;Lymphoma, Follicular

Marketing Authorisation Holder: Secura Bio Limited

EMA Authorisation: 19/05/2021

INN: duvelisib

Indication

Copiktra monotherapy is indicated for the treatment of adult patients with:  Relapsed or refractory chronic lymphocytic leukaemia (CLL) after at least two prior therapies.  Follicular lymphoma (FL) that is refractory to at least two prior  systemic therapies.

Official EMA Resources

View on EMA (ema.europa.eu)

AI Drug & Interaction Analysis

Free account required

Ask Prognia AI about Copiktra — dosing recommendations, drug interactions, and current guideline evidence from ESC, EMA, NICE and more.

Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.