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mondotwin/mondotwin-researcher

v0.7.4

Seven clinical-research skills on mondoTWIN's trial-registry and regulatory-guidance database: benchmark similar trials, count and compare registered trials with read-only SQL, report which endpoints and comparators the trials of an indication used and how they fared, review a protocol section against ICH, draft eligibility criteria from comparable trials, choose endpoints and estimands, and look up ICH or FDA guidance with quoted passages. Includes the mondoTWIN connector (OAuth sign-in).

eligibility-criteria

Draft inclusion and exclusion criteria for a clinical trial from the criteria of comparable registered trials, and propose concomitant-medication exclusions from what those trials prohibit and from the investigational drug's likely interactions with background and commonly co-prescribed drugs. Use when the user asks to write, draft, compare, tighten or broaden eligibility criteria, inclusion/exclusion criteria, or prohibited and restricted medications for a study.

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