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pegylated liposomal irinotecan (Onivyde®)

 

Status: Under consideration by AWMSG Scrutiny Panel

In combination with oxaliplatin, 5-fluorouracil (5-FU) and leucovorin (LV) for the first-line treatment of adult patients with metastatic adenocarcinoma of the pancreas. This medicine was considered by AWMSG Scrutiny Panel on 7th August 2025. It was considered  suitable for assessment by LOWMAG

 

Medicine details

Medicine name pegylated liposomal irinotecan (Onivyde®)
Formulation 4.3 mg/ml concentrate for solution for infusion
Reference number 6200
Indication

As above

Company Servier Laboratories Ltd
BNF chapter Malignant disease & immunosuppression
Assessment type Under consideration
Status Under consideration by AWMSG Scrutiny Panel
Scrutiny Panel meeting date 07/08/2025
NICE guidance

TA1052:Pegylated liposomal irinotecan in combination for untreated metastatic pancreatic cancer (terminated appraisal)

Further information

This medicine was considered by AWMSG Scrutiny Panel on 7 August 2025. 

Pegylated liposomal irinotecan (Onivyde®) is suitable for a full HTA assessment via the Licensed Medicines One Wales Medicines Assessment Group (LOWMAG).

A Welsh Patient Access Scheme (WPAS) has already been agreed through the Commercial Arrangement Scheme Wales Group (CASWG).

Clinicians highlighted the unmet clinical need for this medicine.  This medicine is not routinely available across other UK countries and there is no UK clinical guidance available, it was therefore deemed suitable for full HTA assessment. A full submission has been  requested from the company.

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