Individual Patient Funding Request (IPFR) and One Wales Interim Commissioning Processes. Professor Phil Routledge, Clinical Director AWTTC

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Individual Patient Funding Request (IPFR) and One Wales Interim Commissioning Processes Professor Phil Routledge, Clinical Director AWTTC

All Wales Medicines Strategy Group

Pathways to medicines access in Wales * On NICE work programme? Await NICE guidance Positive recommendation? NHS Wales to fund within 3 months New medicine Licensed for that clinical indication? Has company made a submission to AWMSG? AWMSG appraisal process * There is the facility to appraise before NICE if directed by WG ǂ =Some LHBs have their own unlicensed/off-label processes There is an opportunity for re-appraisal by AWMSG in certain circumstances Some LHBs have price threshold before conducting IPFR ǂ Await company submission (within 3 months of licensing) submission n-endorsement advisory notice on AWMSG Website

IPFR PANELS IN WALES 7 Health Board IPFR Panels 1 national panel (WHSSC)

What is an Individual Patient Funding Request? IPFR A request to a health board to fund NHS healthcare for s who fall outside the range of services and treatments that a health board has agreed to routinely provide This can include a request for any type of healthcare including a specific service, treatment, medicine, device or piece of equipment

IPFR Categories suitable for IPFR A treatment that is either new, novel, developing or unproven and is not within the health board s routine schedule of services and treatment (e.g. A drug that has yet to be approved for use in a particular condition) A treatment that is provided by the health board in certain clinical circumstances but is not eligible in accordance with the clinical policy criteria for that treatment (e.g. Treatment for varicose veins) The patient has a rare or specialist condition that falls within the service remit of the Welsh Health Specialised Services Committee(WHSSC) but in not eligible in accordance with the clinical policy criteria (e.g. Plastic surgery)

IPFR IPFRs conducted since 2012? Year 2012-13 2013-14 2014-15 2015-16. %. %. %. % IPFR (medicines) 406 60 437 59 348 67 309 45 IPFR (medicines) - approved IPFR (treatments) IPFR (treatments) approved Total IPFR Total IPFR approved 216 53 223 51 176 51 176 57 275 40 303 41 173 33 374 55 131 48 160 53 86 50 226 60 681 100 740 100 521 100 683 100 347 51 383 52 262 50 402 59 IPFR system 2014 IPFR Review 7 Present Review

2016-17 Review of IPFR Process It is right that we have a process in Wales to enable access to treatments and devices which are not normally available via the NHS. Each health service in the UK has such a process, with clinical criteria to determine accessibility The NHS Wales process has been improved following a review in 2013-14. A further review will now take place to ensure better consistency of decisions across Wales and make recommendations about what clinical criteria should be applied when determining eligibility Vaughan Gething AM Cabinet Secretary for Health, Well-being and Sport

Methods to achieve access for patient groups Early HTA Interim commissioning Late HTA (if medicine available in England via a commissioning route) Generic name Trade name AWMSG Status MINISTERIAL RATIFICATION NICE STATUS NICE APPRAISAL DATE sorafenib (Nexavar ) Optimised 05/04/2016 t recommended 26/05/2010 recommendation aflibercept (Zaltrap ) t recommended 08/06/2015 t recommended 25/03/2014 eribulin mesilate (Halaven ) Optimised 29/04/2016 t recommended 01/04/2012 recommendation pomalidomide (Imnovid ) Recommended 27/08/2015 t recommended 26/03/2015

One Wales Interim Commissioning Process for licensed medicines * On NICE work programme? Await NICE guidance Positive recommendation (with ratification? NHS Wales to fund within 3 months New medicine Licensed for that clinical indication? Has company made a submission to AWMSG? AWMSG appraisal process * There is the facility to appraise before NICE if directed by WG ǂ =Some LHBs have their own unlicensed/off-label processes There is an opportunity for re-appraisal by AWMSG in certain circumstances Some LHBs have price threshold before conducting IPFR ǂ Company not yet ready for HTA Await company submission (within 3 months of licensing) submission n-endorsement advisory notice on AWMSG Website Meets criteria for one Wales Interim Commissioning? One Wales Interim Commissioning process Positive recommendation (with ratification)? NHS Wales to fund

One Wales Decision Tool for licensed medicines Has an unmet medical /clinical need for the medicine to treat a serious condition been identified NO YES Has the Company agreed to provide appropriate evidence YES Has the holder of the marketing authorisation committed to a health technology appraisal by NICE and / or AWMSG? YES Is it feasible to collect data on outcomes in the period before formal HTA? NO NO NO YES One Wales interim commissioning process to proceed All the conditions in the coloured boxes must be met for the One Wales Process to proceed t suitable for One Wales interim patient cohort decision Please note this only applies for licensed medicines. Unlicensed medicines or offlabel use of a medicine will be considered on a case-by-case basis

One Wales Interim Commissioning Process for off-label use * On NICE work programme? Await NICE guidance Positive recommendation (with ratification? NHS Wales to fund within 3 months New medicine Licensed for that clinical indication? Has company made a submission to AWMSG? AWMSG appraisal process * There is the facility to appraise before NICE if directed by WG ǂ =Some LHBs have their own unlicensed/off-label processes There is an opportunity for re-appraisal by AWMSG in certain circumstances Some LHBs have price threshold before conducting IPFR ǂ Company not yet ready for HTA Await company submission (within 3 months of licensing) submission n-endorsement advisory notice on AWMSG Website ǂ Meets criteria for one Wales Interim Commissioning? One Wales Interim Commissioning process Positive recommendation (with ratification)? NHS Wales to fund

One Wales Interim Pathway Commissioning Group (IPCG) decisions, May 2016 to date Medicine, indication and licensed status IPCG decision 1. Axitinib, post-pazopanib, for advanced renal cell carcinoma (off-label) Use supported 2. Docetaxel in combination with hormone therapy for the treatment of metastatic prostate cancer (off-label) 3. Bevacizumab (7.5 mg) for the 1 st line treatment of advanced ovarian cancer in patients at high risk of disease progression (off-label) 4. Adalimumab (Humira ) for the treatment of paediatric patients with severe refractory uveitis (off-label) 5. Adalimumab (Humira ) for the treatment of adult patients with severe refractory uveitis (off label) 6. Arsenic trioxide (TRISENOX ) for Acute promyelocytic leukaemia - 1st line therapy in patients unsuitable for anthracycline-based therapy (off label) Use supported Use not supported Use supported Use supported Use supported Further medicine-indications for patient cohorts in Wales are being prepared for consideration by IPCG

One Wales Interim Commissioning Points to note One Wales interim commissioning will not apply to medicines that have been appraised by NICE/AWMSG and received a negative recommendation The duration of an interim commissioning decision for licensed medicines will be decided on a case by case basis For unlicensed medicines the One Wales interim commissioning decision will be reviewed annually For unlicensed medicines to be considered there must be no suitably licensed alternative Patient outcomes are to be monitored following a positive decision for both licensed and unlicensed medicines

Conclusions Health technology Appraisal (HTA) remains the most important mechanism to ensure patients can access clinically effective and costeffective medicines in a timely fashion In certain circumstances, the one-wales Interim Commissioning process may allow time to collect outcome data to allow subsequent definitive HTA of licensed medicines/ indications or to establish an all Wales approach for certain off-label indications The individual Patient Funding Request (IPFR) Process may enable s to access treatments and devices not normally available via the NHS. It working is presently being reviewed in Wales

Gail Woodland Acknowledgements Ann-Marie Matthews Karen Samuels Kath Haines Tony Williams Ruth Lang Rosie Spears Jess Davies Rest of the AWTTC team at University Hospital Llandough

Diolch yn Fawr routledgepa@cardiff.ac.uk