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Completed Phase 2 Interventional

A Phase II Study of the Safety and Efficacy of MPSK3169A in Patients With Coronary Heart Disease or High Risk of Coronary Heart Disease

ClinicalTrials.gov ID: NCT01609140

Public ClinicalTrials.gov record NCT01609140. 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 Jun 26, 2026, 12:03 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

A Phase II, Randomized, Placebo-Controlled, Double-Blind Study of the Safety and Efficacy of MPSK3169A in Patients With Coronary Heart Disease or High Risk of Coronary Heart Disease

Study identification

NCT ID
NCT01609140
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Genentech, Inc.
Industry
Enrollment
248 participants

Conditions and interventions

Interventions

  • MPSK3169A Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 80 Years
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
Apr 30, 2012
Primary completion
Apr 30, 2013
Completion
Jun 30, 2013
Last update posted
Nov 1, 2016

2012 – 2013

United States locations

U.S. sites
34
U.S. states
20
U.S. cities
32
Facility City State ZIP Site status
Not listed Goodyear Arizona 85395
Not listed Carmichael California 95608
Not listed Spring Valley California 91978
Not listed Walnut Creek California 94598
Not listed Wildomar California 92595
Not listed Jacksonville Florida 32216
Not listed Ponte Verde Florida 32081
Not listed Boise Idaho 83704
Not listed Indianapolis Indiana 46260
Not listed Iowa City Iowa 52242
Not listed Auburn Maine 04210
Not listed Baltimore Maryland 21209
Not listed Bethesda Maryland 20817
Not listed St Louis Missouri 63110
Not listed Rochester New York 14609
Not listed Wilmington North Carolina 28401
Not listed Fargo North Dakota 58103
Not listed Cincinnati Ohio 45212
Not listed Cincinnati Ohio 45219
Not listed Springdale Ohio 45246
Not listed Oklahoma City Oklahoma 73103
Not listed Tulsa Oklahoma 74136
Not listed Greer South Carolina 29650
Not listed Mt. Pleasant South Carolina 29464
Not listed Spartanburg South Carolina 29303
Not listed Rapid City South Dakota 57701
Not listed Bristol Tennessee 37620
Not listed Knoxville Tennessee 27912
Not listed Boerne Texas 78006
Not listed Dallas Texas 75230
Not listed Dallas Texas 75231
Not listed Houston Texas 77030
Not listed Richmond Virginia 23294
Not listed Wenatchee Washington 98801

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 39 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01609140, 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 Nov 1, 2016 · Synced Jun 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01609140 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →