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The median total duration of expected protection after FDA approval, when accounting for both pre- and post-approval patents and regulatory exclusivities, was 18.3 years (IQR: 16.0-19.4)
Any future Canadian authorization would follow a successful regulatory submission
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For the most up-to-date information on NHS access, eligibility criteria, and service availability, patients are encouraged to visit www.nice.org.uk and www.nhs.uk
