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Term of the Day

Natural history study

A natural history study is a preplanned observational study intended to track the course of a disease over time, identifying demographic, genetic, environmental and other variables that correlate with its development and outcomes in the absence of intervention, or under standard of care. Designs may be retrospective (chart review of existing records) or prospective (longitudinal follow-up of a cohort or registry).

Natural history data is particularly important in rare and paediatric diseases, where randomised placebo-controlled trials may be infeasible or unethical. The FDA (guidance on rare disease natural history studies, 2019) and the EMA accept well-designed natural history studies to define endpoints and biomarkers, identify patient subgroups, estimate sample sizes and, in some cases, serve as external or historical control arms for single-arm trials supporting orphan products.

Because they are non-interventional, natural history studies fall outside the CTR and are governed by national law (for example France's MR-003 or MR-004 reference methodologies) and by the GDPR. They typically involve secondary use of medical records, long-term follow-up, genetic data and small populations in which anonymisation is rarely achievable, so pseudonymisation, a DPIA and a robust research legal basis under Art. 9(2)(j) are essential. Registries maintained by patient organisations or academic consortia raise additional questions of joint controllership and data access governance.

F

First-in-class drugs

A first-in-class drug is a medicine that acts through a new and unique mechanism of action to treat a medical condition, with no approved product working in the same way. The FDA tracks first-in-class approvals as an indicator of innovation; typically between a third and a half of novel drugs approved each year fall into this category. Contrast with best-in-class drugs, which improve on an already validated mechanism.

Because the mechanism is unproven in humans, first-in-class development carries higher scientific and safety risk. Early-phase clinical trials place particular weight on pharmacokinetics, biomarkers of target engagement and careful dose escalation, often under adaptive designs with a data monitoring committee. Regulatory tools such as orphan designation, PRIME (EMA) and Breakthrough Therapy designation (FDA) are frequently sought.

Novel-mechanism programmes tend to collect richer and more exploratory data than confirmatory trials: extensive biomarker panels, genomic profiling, imaging and biobanked samples for future research. This increases the need for clear purpose specification, minimisation of exploratory endpoints, robust consent for future use of samples, and a DPIA that anticipates re-use as the science evolves.