COIOS
Emergent technology building strengthening

New medicines

Which new drugs and vaccines could plausibly move how long people live, whether they reach the people who would benefit, and what the record says about medicines and life expectancy.

Where the evidence stands

A small number of drug classes account for a large share of the fall in mortality over the last fifty years — antihypertensives, statins, antiretrovirals, the vaccines — and the question this driver keeps open is which of the classes now arriving belong on that list. The candidates are identifiable. The GLP-1 drugs are the obvious one and have their own page. Beyond them: the SGLT2 inhibitors, which reduce death and hospital admission in heart failure and kidney disease well beyond the diabetes they were designed for; the RSV vaccines and the long-acting injectables for HIV prevention, each of which changes the population risk of an infection; the anti-amyloid antibodies, whose effect is small; and the first cancer vaccines, in late trials. The historical evidence that pharmaceutical innovation drives life expectancy is real and contested — the estimates depend on how the counterfactual is built — and the trials that establish a drug's effect say nothing about its effect on a population that takes it late, partially or not at all.

That is the second question, and the data are worse. Uptake of a new medicine differs severalfold between countries with similar income, by price, by approval and reimbursement timing, and by the structure of the health system; the countries that link prescribing to outcomes — Denmark, Scotland, Korea — can measure it, and most cannot. Persistence is measured mainly through claims data and is generally poor.

The filing rule: a medicine is filed under the disease it treats when the question is the disease, and here when the question is the medicine — its approval, price, uptake, persistence, safety after launch, or the pipeline as a whole.

Status
building
Direction
strengthening
Would change our view
A national series showing a mortality or morbidity effect attributable to a drug class other than the GLP-1s; evidence that uptake of an effective medicine is failing on price in a high-income country; or a quantified account of the current pipeline's plausible population effect.
Trackers
Gaps
Uptake and persistence data across countries on a common basis; post-launch outcomes for most new classes; the price actually paid rather than the list price; Japan, where approval and uptake follow a different path.

At a glance

Status
building
Direction
strengthening
Last changed
Evidence
Countries

Related drivers

Others we follow in Emergent technology.