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SDF1 Plasmid Treatment for Patients With Peripheral Artery Disease (STOP-PAD)

Primary Purpose

Peripheral Arterial Disease

Status
Unknown status
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
JVS-100
Placebo
Sponsored by
Juventas Therapeutics, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Arterial Disease

Eligibility Criteria

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

Major Inclusion Criteria:

  • Age ≥18
  • Currently receiving standard of care wound treatment (>2 weeks) for chronic wounds or gangrene including as indicated: debridement, pressure offloading, infection control, and/or maintenance of a moist wound environment.
  • Diagnosis of advanced PAD with tissue loss (ulceration and/or dry gangrene) on the foot of the index leg with an ulcer size of at least 0.5 cm2 and <25 cm2. Index wounds on the heel must be <10 cm2 that cannot be probed to bone, have exposed bone or osteomyelitis.
  • Post revascularization intervention inclusion criteria include an attempt at open bypass grafting or endovascular intervention of a popliteal/infrapopliteal lesion(s) on the same leg that has tissue loss without significant improvement in TBI post intervention. The following will be accepted as demonstrating a lack of post intervention toe brachial index (TBI) improvement:

    • TBI ≤ 0.51or;
    • Toe pressure ≤50 mmHg with flat or dampened wave forms or;
    • Skin Perfusion pressure ≤40 mmHg at mid foot level or;
    • TcPO2 ≤40 mmHg
  • Subjects willing to forgo treatment with hyperbaric oxygen, nerve stimulation or sympathectomy for the treatment of advanced PAD from time of consent to 6 months following the initial injection of study drug

Major Exclusion Criteria:

  • Previous major amputation of the leg to be treated or planned major amputation or transmetatarsal amputation within the first month following enrollment.
  • Only a short segment superficial femoral artery lesion - consistent with Inter-Society Consensus for the Management of Peripheral Arterial Disease (TASC II) A or B category, and no infrapopliteal disease
  • Staged or planned intervention in the index leg within 30 days after the index procedure
  • Acute limb-threatening ischemia, trauma, known non-atherosclerotic vascular disease
  • Non-salvageable limb defined as major tissue loss and an unsalvageable foot;
  • Wounds that have decreased in size by >50% between the Screening visit and Day 0.
  • If patient has active infection of the index limb that is being treated, and, in the opinion of treating physician, will not lead to an amputation within the next 3 months, the patient can be enrolled.
  • Inability to safely perform a revascularization procedure due to uncontrolled diabetes or other medical condition.
  • Presence of any other condition that, in the opinion of the investigator, might compromise any aspect of the trial

Sites / Locations

  • Cardiovascular Associates of the Southeast
  • UC DavisRecruiting
  • Cedars-Sinai Heart InstituteRecruiting
  • MedStar Georgetown UH
  • Morton Plant Hosptial - BaycareRecruiting
  • Mount Sinai Medical CenterRecruiting
  • St. Joseph's HospitalRecruiting
  • NorthwesternRecruiting
  • RUMCRecruiting
  • Cardiovascular Institute of the SouthRecruiting
  • St. John Hospital and Medical CenterRecruiting
  • MayoRecruiting
  • Cardiology Associates ResearchRecruiting
  • St. Luke's Mid America Heart InstituteRecruiting
  • Holy Name Medical CenterRecruiting
  • UNCRecruiting
  • NC Heart and Vascular ResearchRecruiting
  • Summa HealthRecruiting
  • Cleveland ClinicRecruiting
  • Metro HealthRecruiting
  • University HospitalsRecruiting
  • Lifespan Health SystemRecruiting
  • VCURecruiting
  • Medical College of WisconsinRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Placebo Comparator

Active Comparator

Placebo Comparator

Arm Label

8 mg JVS-100

8 mg placebo

16 mg JVS-100

16 mg placebo

Arm Description

Biological/Vaccine: JVS-100 Injection Intramuscular Injection

Biological/Vaccine: Placebo Injection Intramuscular Injection

Biological/Vaccine: JVS-100 Injection Intramuscular Injection

Biological/Vaccine: Placebo Injection Intramuscular Injection

Outcomes

Primary Outcome Measures

The composite is designed to quantify clinically significant improvement or worsening over baseline by assigning a score to each patient that represents their overall outcome.
Change from baseline in the composite endpoint at 3 months in all treated (or one JVS-100 dose group) compared to all placebo.
The composite is designed to quantify clinically significant improvement or worsening over baseline by assigning a score to each patient that represents their overall outcome.
Change from baseline in the composite endpoint at 6 months in all treated (or one JVS-100 dose group) compared to all placebo.

Secondary Outcome Measures

Full Information

First Posted
August 6, 2015
Last Updated
November 1, 2016
Sponsor
Juventas Therapeutics, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT02544204
Brief Title
SDF1 Plasmid Treatment for Patients With Peripheral Artery Disease
Acronym
STOP-PAD
Official Title
A Phase 2B Randomized Double Blind Placebo Controlled Study to Evaluate the Safety and Efficacy of JVS-100 Administered by Direct Intramuscular Injection as Adjunct to Revascularization of Infrapopliteal Lesions in Subjects With Advanced Peripheral Artery Disease and Tissue Loss
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Unknown status
Study Start Date
November 2015 (undefined)
Primary Completion Date
September 2017 (Anticipated)
Study Completion Date
November 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Juventas Therapeutics, Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To investigate the efficacy of the administration of JVS-100 delivered via direct intramuscular injections on a 3 month and 6 month composite endpoint of wound progression, healing and limb loss in patients with severe peripheral arterial disease with non-healing chronic wounds who undergo an open bypass grafting or endovascular procedure for treatment of infrapopliteal disease and are dosed within 12 days and 3 months following the procedure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Arterial Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
8 mg JVS-100
Arm Type
Active Comparator
Arm Description
Biological/Vaccine: JVS-100 Injection Intramuscular Injection
Arm Title
8 mg placebo
Arm Type
Placebo Comparator
Arm Description
Biological/Vaccine: Placebo Injection Intramuscular Injection
Arm Title
16 mg JVS-100
Arm Type
Active Comparator
Arm Description
Biological/Vaccine: JVS-100 Injection Intramuscular Injection
Arm Title
16 mg placebo
Arm Type
Placebo Comparator
Arm Description
Biological/Vaccine: Placebo Injection Intramuscular Injection
Intervention Type
Biological
Intervention Name(s)
JVS-100
Intervention Description
Biological/Vaccine: JVS-100 Intramuscular Injection
Intervention Type
Biological
Intervention Name(s)
Placebo
Intervention Description
Biological/Vaccine: Placebo Intramuscular Injection
Primary Outcome Measure Information:
Title
The composite is designed to quantify clinically significant improvement or worsening over baseline by assigning a score to each patient that represents their overall outcome.
Description
Change from baseline in the composite endpoint at 3 months in all treated (or one JVS-100 dose group) compared to all placebo.
Time Frame
3 months
Title
The composite is designed to quantify clinically significant improvement or worsening over baseline by assigning a score to each patient that represents their overall outcome.
Description
Change from baseline in the composite endpoint at 6 months in all treated (or one JVS-100 dose group) compared to all placebo.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Major Inclusion Criteria: Age ≥18 Currently receiving standard of care wound treatment (>2 weeks) for chronic wounds or gangrene including as indicated: debridement, pressure offloading, infection control, and/or maintenance of a moist wound environment. Diagnosis of advanced PAD with tissue loss (ulceration and/or dry gangrene) on the foot of the index leg with an ulcer size of at least 0.5 cm2 and <25 cm2. Index wounds on the heel must be <10 cm2 that cannot be probed to bone, have exposed bone or osteomyelitis. Post revascularization intervention inclusion criteria include an attempt at open bypass grafting or endovascular intervention of a popliteal/infrapopliteal lesion(s) on the same leg that has tissue loss without significant improvement in TBI post intervention. The following will be accepted as demonstrating a lack of post intervention toe brachial index (TBI) improvement: TBI ≤ 0.51or; Toe pressure ≤50 mmHg with flat or dampened wave forms or; Skin Perfusion pressure ≤40 mmHg at mid foot level or; TcPO2 ≤40 mmHg Subjects willing to forgo treatment with hyperbaric oxygen, nerve stimulation or sympathectomy for the treatment of advanced PAD from time of consent to 6 months following the initial injection of study drug Major Exclusion Criteria: Previous major amputation of the leg to be treated or planned major amputation or transmetatarsal amputation within the first month following enrollment. Only a short segment superficial femoral artery lesion - consistent with Inter-Society Consensus for the Management of Peripheral Arterial Disease (TASC II) A or B category, and no infrapopliteal disease Staged or planned intervention in the index leg within 30 days after the index procedure Acute limb-threatening ischemia, trauma, known non-atherosclerotic vascular disease Non-salvageable limb defined as major tissue loss and an unsalvageable foot; Wounds that have decreased in size by >50% between the Screening visit and Day 0. If patient has active infection of the index limb that is being treated, and, in the opinion of treating physician, will not lead to an amputation within the next 3 months, the patient can be enrolled. Inability to safely perform a revascularization procedure due to uncontrolled diabetes or other medical condition. Presence of any other condition that, in the opinion of the investigator, might compromise any aspect of the trial
Facility Information:
Facility Name
Cardiovascular Associates of the Southeast
City
Birmingham
State/Province
Alabama
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chris Huff, MD
Phone
205-795-5193
Facility Name
UC Davis
City
Davis
State/Province
California
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John Laird, MD
Phone
916-734-4156
Facility Name
Cedars-Sinai Heart Institute
City
Los Angeles
State/Province
California
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tim Henry, MD
Phone
310-423-1231
Facility Name
MedStar Georgetown UH
City
Washington
State/Province
District of Columbia
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Paul Kim, MD
Phone
202-444-0793
Facility Name
Morton Plant Hosptial - Baycare
City
Clearwater
State/Province
Florida
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Les Miller, MD
Phone
727-489-2543
Facility Name
Mount Sinai Medical Center
City
Miami
State/Province
Florida
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nirat Beohar, MD
Phone
305-674-2121
Ext
56022
Facility Name
St. Joseph's Hospital
City
Tampa
State/Province
Florida
ZIP/Postal Code
33614
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sai Sadanandan, MD
Phone
813-875-9000
Facility Name
Northwestern
City
Chicago
State/Province
Illinois
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karen Ho, MD
Phone
513-585-1777
Facility Name
RUMC
City
Chicago
State/Province
Illinois
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jeff Snell, MD
Phone
312-942-8707
Facility Name
Cardiovascular Institute of the South
City
Houma
State/Province
Louisiana
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Craig Walker, MD
Phone
985-873-5613
Facility Name
St. John Hospital and Medical Center
City
Detroit
State/Province
Michigan
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tom Davis, MD
Phone
313-343-4714
Facility Name
Mayo
City
Rochester
State/Province
Minnesota
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sanjay Misra, MD
Phone
507-538-6419
Facility Name
Cardiology Associates Research
City
Tupelo
State/Province
Mississippi
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Murray Estess, MD
Phone
662-377-5447
Facility Name
St. Luke's Mid America Heart Institute
City
Kansas City
State/Province
Missouri
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matt Bunte, MD
Phone
816-932-4948
Facility Name
Holy Name Medical Center
City
Teaneck
State/Province
New Jersey
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John Runback, MD
Phone
201-530-7968
Facility Name
UNC
City
Chapel Hill
State/Province
North Carolina
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
William Marston, MD
Phone
919-843-1268
Facility Name
NC Heart and Vascular Research
City
Raleigh
State/Province
North Carolina
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matt Hook, MD
Phone
919-740-4897
Facility Name
Summa Health
City
Akron
State/Province
Ohio
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Justin Dunn, MD
Phone
330-253-8195
Ext
4259
Facility Name
Cleveland Clinic
City
Cleveland
State/Province
Ohio
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mehdi Shishehbor, DO
Phone
216-444-0922
Facility Name
Metro Health
City
Cleveland
State/Province
Ohio
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sanjay Gandhi, MD
Phone
216-778-2714
Facility Name
University Hospitals
City
Cleveland
State/Province
Ohio
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vikram Kashyap, MD
Phone
216-983-4719
Facility Name
Lifespan Health System
City
Providence
State/Province
Rhode Island
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Peter Soukas, MD
Phone
401-793-4105
Facility Name
VCU
City
Richmond
State/Province
Virginia
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Luis Guzman, MD
Phone
804-628-2452
Facility Name
Medical College of Wisconsin
City
Milwauke
State/Province
Wisconsin
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
James Gossett, MD
Phone
414-955-6749

12. IPD Sharing Statement

Citations:
PubMed Identifier
32419594
Citation
Hammad TA, Rundback J, Bunte M, Miller L, Patel PD, Sadanandan S, Fitzgerald M, Pastore J, Kashyap V, Henry TD, Shishehbor MH. Stromal Cell-Derived Factor-1 Plasmid Treatment for Patients With Peripheral Artery Disease (STOP-PAD) Trial: Six-Month Results. J Endovasc Ther. 2020 Aug;27(4):669-675. doi: 10.1177/1526602820919951. Epub 2020 May 18.
Results Reference
derived
PubMed Identifier
30786835
Citation
Shishehbor MH, Rundback J, Bunte M, Hammad TA, Miller L, Patel PD, Sadanandan S, Fitzgerald M, Pastore J, Kashyap V, Henry TD. SDF-1 plasmid treatment for patients with peripheral artery disease (STOP-PAD): Randomized, double-blind, placebo-controlled clinical trial. Vasc Med. 2019 Jun;24(3):200-207. doi: 10.1177/1358863X18817610. Epub 2019 Feb 21.
Results Reference
derived

Learn more about this trial

SDF1 Plasmid Treatment for Patients With Peripheral Artery Disease

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