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IMFINZI (durvalumab) UK Prescribing Information
IMJUDO (tremelimumab) ▼ UK Prescribing Information
Adverse Event Reporting

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Dosing & Administration

 

Find your STRIDE

Single dose IMJUDO (tremelimumab) + IMFINZI (durvalumab), followed by regular interval IMFINZI monotherapy every 4 weeks for the 1L treatment of advanced or unresectable HCC.1-3

STRIDE (Single Tremelimumab Regular Interval Durvalumab)

STRIDE offers a dual immunotherapy regimen with a single dose IMFINZI + IMJUDO, followed by regular interval IMFINZI monotherapy every 4 weeks for the 1L treatment of advanced or unresectable HCC:1-3

Diagram showing the STRIDE dosing regimen: single dose IMJUDO + IMFINZI, followed by IMFINZI monotherapy every 4 weeks Diagram showing the STRIDE dosing regimen: single dose IMJUDO + IMFINZI, followed by IMFINZI monotherapy every 4 weeks

Dosing, preparation of solution and administration:

Dosing

dosing icon

Dose escalation or reduction is not recommended. Dose withholding or discontinuation may be required based on individual safety and tolerability1,2

Preparation
of solution

dosing icon

Prior to administration IMFINZI and IMJUDO must be diluted; for instructions on dilution of the medicinal products please consult 6.6 of the SmPC for IMFINZI and IMJUDIO, respectively1,2


IMFINZI and IMJUDO are both supplied as single-use vials; IMFINZI contains 500mg /10ml or 120mg / 2.4ml and IMJUDO contains 300mg / 15 ml or 25mg /1.25ml1,2

Administration

dosing icon

IMFINZI and IMJUDO are each administered as separate 60minute IV infusions on the same day, treatment must be initiated and supervised by physician experienced in the treatment of cancer.1,2

Infusion-related reactions with STRIDE were observed in 1.3% of patients (pooled data in 462 patients with HCC from HIMALAYA and Study 22)1,2

Please refer to the SmPC for IMFINZI and IMJUDO for further information on storage, dilution and administration instructions

IMJUDO SmPC
IMFINZI SmPC

HCC, hepatocellular carcinoma; STRIDE, single tremelimumab regular interval durvalumab; 1L, first-line.

  1. IMFINZI, Summary of Product Characteristics.
  2. IMJUDO, Summary of Product Characteristics.
  3. Abou-Alfa GK. et al. NEJM Evid. 2022;1(8).

GB-64281 | April 2025

Adverse events should be reported. Reporting forms and information can be found at http://www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to AstraZeneca by visiting https://contactazmedical.astrazeneca.com/ or by calling ‌‌‌0‌‌‌8‌‌‌‌‌0‌‌‌‌0‌‌‌ ‌‌7‌‌‌‌‌‌8‌‌‌3‌‌‌ ‌‌0‌‌‌‌‌0‌‌‌‌3‌‌‌‌3‌‌‌.

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