/euctis/trials

POST /api/euctis/trials

Price: 20 credits

Full CTIS register record of one authorised EU/EEA clinical trial: titles, sponsors and funding, medical conditions with their MedDRA terms, therapeutic areas, objectives, primary and secondary end points, inclusion and exclusion criteria, the recruited population, investigational products with their ATC codes and marketing authorisations, study periods and arms, every member state's authorisation decision, recruitment dates and trial sites, the application history, the trial event timeline, temporary halts, unexpected events, urgent safety measures, corrective measures, the published document list and the submitted result documents.

How to use it

One trial number resolves to exactly one record, unlike the eudract register where one EudraCT number spans a record per member state — here the per-state detail is inside `member_states`, which is where recruitment dates, sites and national decisions live rather than at the top level. `result_documents` and `clinical_study_reports` are submission metadata: the result content itself is a PDF this endpoint does not return, and `documents` likewise lists what is published without fetching it. Use `nct_number`, `who_universal_trial_number` and `eudract_number` to join a trial to clinicaltrials, ictrp and eudract. A trial number that is well formed but unknown answers 412, so a 412 means the trial is not in CTIS rather than that the number was mistyped.

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