This website is for UK Healthcare Professionals only

This promotional website is for UK Healthcare Professionals involved in the management of haematological malignancies. Adverse event reporting information can be found below.

Tepkinly is licensed
for 3L+ DLBCL

Tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large B‑cell lymphoma (DLBCL) after two or more lines of systemic therapy.1

Tepkinly has a conditional marketing authorisation
- further data awaited.

You are advised to read the Prescribing Information and Summary of Product Characteristics, accessible via the links above, to evaluate patient suitability for Tepkinly.

Adverse event reporting information can be found at the bottom of this page.

Tepkinly is licensed for 3L+ DLBCL

Tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large B‑cell lymphoma (DLBCL) after two or more lines of systemic therapy.1

Tepkinly has a conditional marketing authorisation
- further data awaited.

You are advised to read the Prescribing Information and Summary of Product Characteristics, accessible via the links above, to evaluate patient suitability for Tepkinly.

Adverse event reporting information can be found at the bottom of this page.

By clicking the link above, you will leave the AbbVie Pro website and be taken to the eMC PI portal website.

Abbreviations

CNS=clinical nurse specialist; R/R=relapsed/refractory.

 

References

  1. Tepkinly Summary of Product Characteristics.

 

UK-EPCOR-240402. Date of preparation: January 2025.

Adverse events should be reported. Reporting forms and information can be found at yellowcard.mhra.gov.uk.

Adverse events should also be reported to AbbVie on GBPV@abbvie.com