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Serp-1 for the Treatment of Acute Coronary Syndrome

Primary Purpose

Unstable Angina, Coronary Atherosclerosis, Coronary Restenosis

Status
Terminated
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Serine proteinase-1 (Serp-1)
Sponsored by
Viron Therapeutics Inc
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Unstable Angina focused on measuring Anti-inflammatory agents, unstable plaque, acute coronary syndrome

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Established diagnosis of unstable angina or NSTEMI with one or more episodes of angina in the 24 hours before hospital admission Scheduled for PCI Exclusion Criteria: CABG within 6 months Acute ST elevation, eligible for thrombolysis on initial examination Coronary lesions with total thrombotic occlusions Current immunosuppressant therapy

Sites / Locations

  • Washington Hospital Center
  • University of Florida
  • Spectrum Health
  • Victoria Heart Institute
  • Foothills Medical Center
  • London Health Sciences Centre
  • University of Ottawa Heart Institute
  • Montreal Heart Institute

Outcomes

Primary Outcome Measures

Safety (Adverse events collected until 6 months post-dose)

Secondary Outcome Measures

Inflammatory marker analysis
MACE
Restenosis at 6 months

Full Information

First Posted
October 19, 2005
Last Updated
February 5, 2009
Sponsor
Viron Therapeutics Inc
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1. Study Identification

Unique Protocol Identification Number
NCT00243308
Brief Title
Serp-1 for the Treatment of Acute Coronary Syndrome
Official Title
A Phase 2, Multicentre, Double-Blind, Placebo-Controlled, Dose Escalating Trial of the Safety, Pharmacokinetics, and Biological Activity of 3 Consecutive Daily Doses of Serp-1 When Added to Conventional Therapy in Patients With Acute Coronary Syndromes (Non ST-Elevation Myocardial Infarction and/or Unstable Angina)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2009
Overall Recruitment Status
Terminated
Why Stopped
Third dose group not recruited due to slow enrollment.
Study Start Date
October 2005 (undefined)
Primary Completion Date
July 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Viron Therapeutics Inc

4. Oversight

5. Study Description

Brief Summary
Males and females aged 18-80 years who present with ACS (unstable angina and non ST-elevation MI) defined as one or more episodes of angina lasting at least 5 minutes in the last 24 hours before admission and greater than 0.05 mV of presumed new ST-segment depression in at least 2 contiguous ECG leads OR, angina and per confirmatory angiogram, has been scheduled for percutaneous coronary angioplasty. The primary objective of this study is to evaluate the safety of Serp-1 injection when administered in 3 daily doses to patients undergoing conventional therapy for Acute Coronary Syndrome (ACS) requiring early intervention.
Detailed Description
A total of 72 subjects will be enrolled, separated into 3 dose groups and centrally randomized in a 3:1 ratio of Serp-1 injection to placebo control.Subjects will receive Serp-1 by intravenous (IV) bolus injection daily for 3 days, at dose levels of 5.0, 15, and 50 ug/kg/dose or placebo (0.9% normal saline) added to any prescribed therapy for ACS. Serp-1 will be administered as a single IV bolus injection. The initial IV bolus dose is administered immediately preceding the PCI procedure with subsequent doses administered 24 and 48 hours later.Subjects will be evaluated for adverse events, serum inflammatory markers and restenosis rates at 6 months post-dose.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Unstable Angina, Coronary Atherosclerosis, Coronary Restenosis
Keywords
Anti-inflammatory agents, unstable plaque, acute coronary syndrome

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
72 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Serine proteinase-1 (Serp-1)
Primary Outcome Measure Information:
Title
Safety (Adverse events collected until 6 months post-dose)
Secondary Outcome Measure Information:
Title
Inflammatory marker analysis
Title
MACE
Title
Restenosis at 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Established diagnosis of unstable angina or NSTEMI with one or more episodes of angina in the 24 hours before hospital admission Scheduled for PCI Exclusion Criteria: CABG within 6 months Acute ST elevation, eligible for thrombolysis on initial examination Coronary lesions with total thrombotic occlusions Current immunosuppressant therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexandra Lucas, MD
Organizational Affiliation
Chief Clinical Officer- Viron Therapeutics
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Jean-Claude Tardif, MD
Organizational Affiliation
Director- Montreal Heart Institute Research Centre
Official's Role
Study Chair
Facility Information:
Facility Name
Washington Hospital Center
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20010
Country
United States
Facility Name
University of Florida
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32610-0277
Country
United States
Facility Name
Spectrum Health
City
Grand Rapids
State/Province
Michigan
ZIP/Postal Code
49525
Country
United States
Facility Name
Victoria Heart Institute
City
Vicotria
State/Province
British Columbia
ZIP/Postal Code
V8R 4R2
Country
Canada
Facility Name
Foothills Medical Center
City
Calgary
State/Province
Ontario
ZIP/Postal Code
T2N 2T9
Country
Canada
Facility Name
London Health Sciences Centre
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5C1
Country
Canada
Facility Name
University of Ottawa Heart Institute
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1Y 4W7
Country
Canada
Facility Name
Montreal Heart Institute
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H1T 1C8
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
21062996
Citation
Tardif JC, L'Allier PL, Gregoire J, Ibrahim R, McFadden G, Kostuk W, Knudtson M, Labinaz M, Waksman R, Pepine CJ, Macaulay C, Guertin MC, Lucas A. A randomized controlled, phase 2 trial of the viral serpin Serp-1 in patients with acute coronary syndromes undergoing percutaneous coronary intervention. Circ Cardiovasc Interv. 2010 Dec;3(6):543-8. doi: 10.1161/CIRCINTERVENTIONS.110.953885. Epub 2010 Nov 9.
Results Reference
derived

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Serp-1 for the Treatment of Acute Coronary Syndrome

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