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      • This website is for GB Haemato-Oncology Healthcare Professionals only.

      Tepkinly▼ (epcoritamab)

      I

      TEPKINLY PRESCRIBING INFORMATION
      SUMMARY OF PRODUCT CHARACTERISTICS
      PATIENT CARD

      Tepkinly is now
      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 now 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.

      UK-EPCOR-230021 | January 2024

      button nice v4

      Recommendations include:

      Tepkinly is recommended as an option for treating relapsed or refractory DLBCL
      in adults after 2 or more systemic treatments in adults, only if they have
      previously had polatuzumab vedotin or it is contraindicated or not tolerated.

      Tepkinly is only recommended if the company provides it
      according to the commercial arrangement.

      Click here to access the full guidance on the NICE website

      This button links to an external website which is not under the control of AbbVie.
      AbbVie is not responsible for the content on this site or any further links from the site.

      NICE publishes recommendations for Tepkinly in 3L+ DLBCL2

      Recommendations include:

      Tepkinly is recommended as an option for treating relapsed or refractory DLBCL in adults after 2 or more systemic treatments in adults, only if they have previously had polatuzumab vedotin or it is contraindicated or not tolerated.

      Tepkinly is only recommended if the company provides it according to the commercial arrangement.

      Click here to access the full guidance on the NICE website

      This button links to an external website which is not under the control of AbbVie.
      AbbVie is not responsible for the content on this site or any further links from the site.

      Welcome to AbbVie Pro for Tepkinly in 3L+ DLBCL

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      Discover how Tepkinly could be a new treatment option for your patients with 3L+ DLBCL by exploring the data and practical resources provided.

      FRONTIERS is a programme of AbbVie promotional events and resources for GB healthcare professionals involved in the management of haematological malignancies.

       
      Develop your knowledge with FRONTIERS events, insights and resources 
      Learn from leading experts and practice pioneers

      Downloadable materials
      FrontierLogo

      FRONTIERS is a programme of AbbVie promotional events and resources for GB healthcare professionals involved in the management of haematological malignancies.

       
      Develop your knowledge with FRONTIERS events, insights and resources 
      Learn from leading experts and practice pioneers

      Downloadable materials
      FrontierLogo

      Tepkinly is a subcutaneous T-cell engaging CD3xCD20 bispecific antibody1,3,4

      divider 2

      Tepkinly is a humanised IgG-1 bispecific antibody that binds to a specific extracellular epitope of CD20 on B cells and to CD3 on T cells1

      By simultaneously binding CD20-expressing B cells and CD3-expressing T cells, Tepkinly induces specific T-cell activation and T-cell-mediated killing of the CD20-expressing cancer cells1

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      image and text

      Tepkinly's Fc region is silenced for direct immune effector mechanisms1

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      In preclinical studies, Tepkinly demonstrated T-cell-mediated lysis of CD20-expressing cells4

      Downloadable resource

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      DADownload

      Tepkinly dosing and administration guide

      A digital guide to optimal dosing and administration of Tepkinly. The guide also provides instructions on how to prepare and store Tepkinly correctly, along with important safety information.

      Abbreviations

      3L+=third line plus; BsAb=bispecific antibody; CD3=cluster of differentiation 3; CD20=cluster of differentiation 20; DLBCL=diffuse large B-cell lymphoma; Fc region=fragment crystallization region; IgG-1=Immunoglobulin G1; NICE=National Institute for Health and Care Excellence.

      References

      1. Tepkinly GB Summary of Product Characteristics. 
      2. NICE 2024. Epcoritamab for treating relapsed or refractory diffuse large B-cell lymphoma after 2 or more systemic treatments. Available at https://www.nice.org.uk/guidance/ta954 (Accessed: March 2024).
      3. Thieblemont C et al. J Clin Oncol. 2022; 41(12): 2238-47.
      4. Engelberts P et al. EBioMedicine. 2020; 52: 102625.

      References

      1. Tepkinly GB Summary of Product Characteristics. 
      2. NICE 2024. Epcoritamab for treating relapsed or refractory diffuse large B-cell lymphoma after 2 or more systemic treatments. Available at https://www.nice.org.uk /guidance/ta954 (Accessed: March 2024).
      3. Thieblemont C et al. J Clin Oncol. 2022; 41(12): 2238-47.
      4. Engelberts P et al. EBioMedicine. 2020; 52: 102625.
      TEPKINLY PRESCRIBING INFORMATION

      UK-EPCOR-240114. Date of preparation: March 2024.

      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 [email protected]

      Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk or via the MHRA Yellow Card app, available in the Google Play or Apple App Stores. Adverse events should also be reported to AbbVie on [email protected]

       

      This website is for GB Haemato-Oncology Healthcare Professionals only.

      UK-EPCOR-230056. Date of Preparation: October 2023. This website has been developed and funded by AbbVie Ltd.

      © 2023 AbbVie Ltd. All rights reserved. Registered Number: 08004972 England.