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Clinical Trials in the USA / NCT01088386
Enrolling by invitation Observational

Zyprexa® Relprevv™ Patient Care Program

NCT01088386 · tracked via the Priya Life Science USA tracker
Sponsor
Eli Lilly and Company
Phase
Observational
Started
2010-03-03
Last updated
2026-01-28

Condition(s) studied

Schizophrenia

Study summary

The goal of the Zyprexa Relprevv Patient Care Program is to mitigate the risk of negative outcomes associated with Zyprexa Relprevv post-injection delirium/sedation syndrome (PDSS).

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Any patients receiving Zyprexa Relprevv enrolled in Zyprexa Relprevv Patient Care Program Exclusion Criteria: * Any patient not receiving Zyprexa Relprevv

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
United BioSource Corporation Blue Bell Pennsylvania

More Eli Lilly and Company trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT01088386 on ClinicalTrials.gov ↗ ← All trials in the USA