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Zyprexa® Relprevv™ Patient Care Program

← catalyst calendar

NCT01088386

Sponsored by Eli Lilly and Company (industry) · LLY — their whole pipeline →.

Phase
Status
Enrolling by invitation
Study type
Observational
Enrollment
4,000estimated
Sites
1
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2010-03-03actualWhen the study began enrolling
Primary completionJun 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJun 2026estimatedThe whole study's end, after follow-up
First posted2010-03-17estimatedWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-01-28actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Schizophrenia

Primary outcome

what the primary-completion date above is the date OF
Incidence per injection and per patient of post-injection delirium/sedation syndrome (PDSS) events
measured Baseline to end of study

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