Jaypirca

pirtobrutinib · Eli Lilly Nederland B.V.
CONDITIONAL APPROVAL AUTHORISED IN THE EU

What Jaypirca is used for

Jaypirca as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL) who have been previously treated with a Bruton’s tyrosine kinase (BTK) inhibitor. Jaypirca as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukaemia (CLL).

Approved use, as published by the European Medicines Agency.

What the labels mean

  • Conditional approval: approved on less complete data because the need is high; more data must follow.

Key facts

Brand
Jaypirca
Active substance
pirtobrutinib
Disease area
Lymphoma, Mantle-Cell
Medicine group
Antineoplastic agents;Protein kinase inhibitors
ATC code
L01
Marketing authorisation holder
Eli Lilly Nederland B.V.
Authorised in the EU since
2023

Official information

In the USA

Same active substance: Jaypirca

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Jaypirca used for?

Jaypirca as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL) who have been previously treated with a Bruton’s tyrosine kinase (BTK) inhibitor. Jaypirca as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukaemia (CLL).

What is the active substance in Jaypirca?

Jaypirca contains pirtobrutinib.

Who makes Jaypirca?

The EU marketing authorisation holder is Eli Lilly Nederland B.V..

Source: European Medicines Agency medicines data (ema.europa.eu), reproduced with acknowledgement of the source. Page made 5 November 2026 by Satya Babu.

← All specialty medicines, EU

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