Skip to content

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).

endpoint-and-estimand

Summarise which primary and key secondary endpoints comparable registered trials used and at which time points, and draft the estimand for a trial objective following ICH E9(R1) (treatment, population, variable, intercurrent events with their strategies, population-level summary). Use when the user is choosing or justifying a primary or secondary endpoint, asks what similar trials measured and when, or asks to define, check or write an estimand or an intercurrent-event strategy.

Read SKILL.md at the source

Pinned to revision 345a8357bd24, so it is the text this page describes rather than whatever the author pushed since.

Files

Every link opens the file at its source, pinned to the revision this page describes.