Publications

CAR-T cell therapy: implications of recent Yescarta and Kymriah announcements for manufacturers and assessment agencies

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CADTH issues its first CAR-T assessment

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Impact of European Medicines Agency clinical trial transparency policies on HTA decisions in the UK

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Can we satisfactorily measure the clinical value of new classes of oncology agents with a single summary measure?

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Do countries with similar GDPs and health expenditures reimburse the same cancer drugs?

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What role does the patient perspective play in determining access to innovative therapies?

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The impact of patient characteristics and disease-specific factors on first-line treatment decisions for BRAF-mutated melanoma: results from a European panel study

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The role of companion diagnostics in HTAs of drugs in France, Germany, and the UK

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Measuring survival benefit in health technology assessment in the presence of nonproportional hazards

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What is the impact of orphan drug re-assessments in Germany on their additional benefit and price?

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The difference between regulatory and market access decisions on treatment availability for new drugs in six common cancers across Australia, Canada, and Europe

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Mapping patient involvement in NICE appraisals of oncology products

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Impact of EMA clinical trial transparency policies on HTA decisions in Germany

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Do market withdrawals impact patient access to treatment in Germany?

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Can we satisfactorily measure the clinical value of new classes of oncology agents with a single summary measure?

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Assessing the implications of the NICE budget impact test: how many oncology regimens will be affected and what will be the impact on patient outcomes?

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