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ClinicalTrials.gov

ClinicalTrials.gov is the master list of clinical trials. Every trial on this site links to its record.

Mandatory registration for US trials; API v2 provides structured access to eligibility, arms, outcomes, and results. The backbone for any trial-matching tool.

Holds
Registry and results database of >500,000 clinical studies worldwide.
Licence
Public domain (US Government)
Maintainer
NIH / NLM

Connected

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Pages like this

not linked directly; found by shared links

technologies

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companies

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ideas

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A $50 million prize for the first off-patent drug proven to extend cancer survivalA live 'seats available' feed for trial slots, like airline inventoryA plain-language summary of every cancer trial result within a yearA public map of trial deserts to steer where new sites openA public transparency score for every trial sponsor, used by sites and patientsA shared compound library that rare cancer researchers can actually useA single oncology trial data trust with mandatory deposit within eighteen monthsA standing rulebook for one-patient treatmentsActually fine sponsors who do not post trial resultsAn annual map of high-burden questions that nobody is fundingAn open forecasting tournament on which combination trials will succeedAn open knowledge graph linking trials, results, biomarkers, drugs and recommendationsAutomatically detect when a trial changes its outcomes after the factDefault-inclusive eligibility: sponsors must justify every exclusion criterionDeposit trial results as structured data, not just PDFsEnforce individual participant data sharing as a condition of publication and fundingEvery tumour sequencing report lists open, nearby, matched trials pulled liveGuidelines list the open trials at every decision point, updated monthlyLive tracker of the lag from first approval to real availability in every countryMap trial case report forms to the registry standard so trial and routine data joinNo new trial approval until the sponsor has reported its old onesOne clinical trial application accepted by regulators in every major regionOne ethics approval and one consent form for a platform trial across countriesOne national master contract and budget template for all cancer trialsOne standing umbrella trial for all rare cancers in a countryPay for residual disease tests only inside a trial or registryPay investigators for finishing and publishing trials, not for enrolling patientsPool every immunotherapy trial's biomarker data into one commonsPre-register biomarker validation studies the way trials are registeredPublish why patients were screened out of each trialRandomise inside the registry that already follows every patientRequire every oncology candidate to publish how much reaches the brainSet trial enrolment targets from who actually gets the disease, and publish progress liveShared concurrent control arms across sponsors' trials in the same settingStop failing trials earlier with pre-registered aggressive futility rulesTrial matching inside the electronic record at the moment a treatment is chosen

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