Delivered to your Trust or directly to your Patient:

Kinpeygo®

Kinpeygo® – the first and only disease-modifying treatment approved across Europe and by NICE specifically for use in IgA nephropathy1,2

Kinpeygo® is indicated for the treatment of primary immunoglobulin A (IgA) nephropathy (IgAN) in adults at risk of rapid disease progression with urine protein-to-creatinine ratio (UPCR) ≥ 1.5g/gram

Prescribing Information can be found here
Adverse Event reporting information can be found in the footer

Find out more about Kinpeygo®

Request a visit from our Medical Science Liaison Team or Healthcare Partnership Manager Team

How to order Kinpeygo®

Order via HealthNet Homecare for delivery to your Trust or direct to your patient.

Clinical Resource:

 

Kinpeygo®
Formulary Guide

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Kinpeygo®
NICE Guidance

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Kinpeygo®
Pharmacy Leaflet

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Kinpeygo®
Clinician Leaflet

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Educational Webinars

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Kinpeygo® Patient Support Leaflet

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Visit the Kinpeygo® Patient Website

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References

1. European public assessment report (EPAR) Kinpeygo. EMA/570757/2022, last revised 05/2022. 2. Overview | Targeted-release budesonide for treating primary IgA nephropathy | Guidance | NICE. https://www.nice.org.uk/guidance/ta937 (Published: 20 December 2023).

Information

For information on our products please visit EMChttps://www.medicines.org.uk/emc/ and search the product for a Summary of Product Characteristics

Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to Thornton and Ross Limited by emailing thorntonross@medinformation.co.uk or by calling 01484 848164.

UK-MULT-122e(3) | Date of Preparation: November 2024

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The information on our Healthcare Professional Website is solely intended for UK Healthcare Professionals and contains promotional information. Click here to return to our main public site.

For information on our products please visit EMC and search the product for a Summary of Product Characteristics.

Adverse events should be reported. Reporting forms and information can be found at: www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Thornton and Ross Limited by emailing thorntonross@medinformation.co.uk or by calling 01484 848164.