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Completed Phase 2 Interventional

Safety and Efficacy Study of KAI-9803 to Treat Subjects With ST Elevation Myocardial Infarction [Heart Attack]

ClinicalTrials.gov ID: NCT00785954

Public ClinicalTrials.gov record NCT00785954. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 3:39 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Inhibition of Delta-protein Kinase C for the Reduction of Infarct Size in Acute Myocardial Infarction

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine whether KAI-9803 is safe and effective in reducing infarct size in subjects with ST elevation myocardial infarction (heart attack) undergoing a percutaneous coronary intervention (PCI). A select number of sites will also participate in a substudy where eligible patients will undergo an additional procedure;cardiac magnetic resonance imaging.

Study identification

NCT ID
NCT00785954
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
KAI Pharmaceuticals
Industry
Enrollment
1,180 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2008 (Type not available)
Primary completion
Jul 2010 (Actual)
Completion
May 2011 (Actual)
Last update posted
Sep 2, 2011

2008 – 2011

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
Not listed Huntsville Alabama 35801 —
Not listed Escondido California 92025 —
Not listed Torrance California 90509 —
Not listed Tampa Florida 33613 —
Not listed Atlanta Georgia 30309 —
Not listed Downers Grove Illinois 60515 —
Not listed Lombard Illinois 60148 —
Not listed Peoria Illinois 61602 —
Not listed Valparaiso Indiana 46383 —
Not listed Omaha Nebraska 68131 —
Not listed Williamsville New York 14221 —
Not listed Greensboro North Carolina 27410 —
Not listed High Point North Carolina 27262 —
Not listed Zanesville Ohio 43701 —
Not listed Oklahoma City Oklahoma 77030 —
Not listed Beaver Pennsylvania 15009 —
Not listed Danville Pennsylvania 17822 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 109 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00785954, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 2, 2011 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00785954 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →