Pre.sentient
All updates
Insights4 August 2026

Optimal Stoppage of Doomed Processes

Most clinical trials fail, and a failing trial keeps enrolling patients who cannot benefit while costing money. Yet a substantial share of commercial trials run no interim look at all, and those that do typically check only once, near the halfway point, stopping if the treatment appears futile.

Chart showing trial time recovered through earlier stopping

Most clinical trials fail, and a failing trial keeps enrolling patients who cannot benefit while costing money.

Yet a substantial share of commercial trials run no interim look at all, and those that do typically check only once, near the halfway point, stopping if the treatment appears futile.

But deciding to stop is not stopping: a committee must convene, unblind and act. That delay creates a horizon beyond which looking is pointless, because no time remains to recover.

We ask what is lost by looking only once - and what is lost by never looking at all.

A single look must be either early, when the evidence is weak, or late, when little time is left. Continuous monitoring need not choose a specific time and it reduces false futility against a single look; and protects alpha.

For a canonical 36-month trial, continuous monitoring ends a doomed trial about 20 months early, against 13 for a single look at midpoint.

Read the full paper: Optimal Stoppage of Doomed Processes

Read next

More from Pre.sentient

All updates
InsightsFIFA World Cup Rule Change Proposal - Leading By 5 Goals Leads to an Automatic WinLeading by 5 goals is significant. So significant in fact that in the entire 163 year old history of the modern game a 5 goal lead has never been overturned in a top flight game. Maybe time for a rule change?15 July 2026InsightsPresentient Proposes Pilot in Response to FDAs AI-Enabled Optimization of Early-Phase Clinical Trials Pilot Program RFIThe FDA comments clarify how the FDA anticipate BRAKES being deployed; sponsors seeking to use BRAKES in the context of a specific clinical trial are to engage with the FDA via individual IND submissions.30 June 2026InsightsWhitepaper: BRAKES helps trials stop years earlierThe BRAKES platform accelerates decision-making by months to years while eliminating operational bias.19 January 2026