Study of VF001-DP in Patients With Chronic Venous Leg Ulcers

A Prospective, Multi-Center, Double-Blind, Randomized, Placebo-Controlled Trial Comparing Two Doses of VF001-DP to Placebo as an Adjunct to Standard Care in Patients With Chronic Venous Leg Ulcers

The purpose of this study is to determine if VF001-DP improves wound healing in chronic venous leg ulcers compared to standard care only.

Study Overview

• Status: Unknown
• Conditions: Pathologic Processes; Cardiovascular Diseases; Vascular Diseases; Skin Diseases; Ulcer; Leg Ulcer; Skin Ulcer; Varicose Ulcer
• Intervention / Treatment: Biological: Placebo; Biological: VF001-DP LD; Biological: VF001-DP HD

Detailed Description

Objective: The objective of this study is to demonstrate the effectiveness and safety of VF001-DP as an adjunct to standard care (SC) in the treatment of chronic venous leg ulcers (VLUs) compared to Placebo with SC over the course of the 12-week Treatment Phase.

Design: This study is a multi-center, randomized, double-blind, placebo-controlled dose-response study designed to evaluate VF-001-DP as an adjunct to SC, versus Placebo and SC in the treatment of chronic VLUs. The SC therapy for VLUs is a moisture retentive ulcer dressing and multi-layer compression therapy. Mepitel® and Coban2® have been chosen to be used as SC in this trial.

The study will have three (3) phases: Screening (2 weeks), Treatment Phase (12 weeks) and Follow-Up (12 weeks).

Only patients whose study ulcer does not exhibit more than 30% change (increase or decrease) in ulcer size post-debridement between Screening Phase Visit (S1) and Treatment Phase Visit (T1) and who continue to meet eligibility criteria at T1 will be randomized to receive either the Active Treatment group (VF001-DP low or high dose plus SC) or the Control Treatment group (Placebo plus SC) in a ratio of 1:1:1.

Treatment: Eligible patients will be assigned to one of the following treatment groups:

• Placebo and SC
• VF001-DP (14 micrograms per treatment) and SC (low dose [LD])
• VF001-DP (140 micrograms per treatment) and SC (high dose [HD]).

The investigational product (IP), i.e., VF001-DP and placebo, will be supplied in 1 mL syringes each containing 0.5 mL of either VF001-DP or Placebo.

The IP contains parts of normal vitronectin and Insulin-like growth factor 1 (IGF-I) combined in a single protein (vitronectin, amino acids 1-64 of the human sequence and IGF-I amino acids 1-70 of the human sequence), 14 μg or 140 μg protein in 0.5 mL of Phosphate Buffered Saline, pH 7.2. VF001-DP is manufactured utilizing an expression vector system in yeast to Good Manufacturing Practice (GMP) and is not made with and does not include any products of human or animal origin.

Number of Patients: It is planned to recruit 168 patients (56 per treatment group) at 26 centres in USA for this study.

• Study Type: Interventional
• Enrollment (Anticipated): 156
• Phase: Phase 2

Contacts and Locations

Study Locations

• United States
  • California
    • Carlsbad, California, United States, 92130
      • ILD Research Center
    • Fresno, California, United States, 93721
      • Limb Preservation Platform, Inc.
    • Laguna Hills, California, United States, 24012
      • Alliance Research Centers
    • Los Angeles, California, United States, 90057
      • Foot and Ankle Clinic
    • Martinez, California, United States, 94553
      • Center for Clinical Research
    • Sacramento, California, United States, 95628
      • Sacramento Foot Ankle Cente
    • San Francisco, California, United States, 94115
      • Bay Area Foot Care
    • San Francisco, California, United States, 94705
      • Bay Area Foot Care
    • Vacaville, California, United States, 95687
      • NorthBay Center for Wound Care
  • Florida
    • Miami, Florida, United States, 33136
      • University of Miami Hospital
    • Miami, Florida, United States, 33143
      • Doctor Research Network (Dr Hanft)
    • Miami, Florida, United States, 33176
      • Miami Dade Medical Research Center (Dr Oliva)
    • Miami, Florida, United States, 33176
      • Spotlight Research Centre
    • North Miami Beach, Florida, United States, 33169
      • Barry University School of Podiatric Medicine
  • Nevada
    • Las Vegas, Nevada, United States, 89119
      • Advanced Foot and Ankle Center
  • North Carolina
    • Chapel Hill, North Carolina, United States, 27599
      • University of North Carolina - Chapel Hill
  • Pennsylvania
    • Wyomissing, Pennsylvania, United States, 19610
      • Center for Advanced Wound Care PC

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. At least 18 years old.
2. Ankle-Brachial Pressure Index (ABI) ≥0.80. (Calculations will be made using measurements from both posterior tibial and dorsalis pedis arteries as well as both arms).
3. Presence of VLUs extending through the full thickness of the skin but not down to muscle, tendon or bone. In the case of more than one ulcer, the largest ulcer (compliant with study criteria) will be chosen as the study ulcer and treated in the study. Other ulcerations, if present on the same leg must be at least 2 cm apart from the study ulcer.
4. Venous disease confirmed by Doppler ultrasonography to demonstrate reflux of >0.5 seconds in saphenous (great or small), calf perforators or the deep venous system. Patients with prior venous surgery (i.e., varicose vein stripping, endovenous ablation) may be included if they still demonstrate significant reflux in a remaining venous segment and the ulcer continues to suffer poor healing because of venous hypertension.
5. Ulcer which has been present and treated with standard care (moisture retentive ulcer dressings and compression bandaging not limited to Mepitel® and Coban2®) for at least one month prior to the initial Screening Visit.

6. Moderate severity ulcer at the T1 visit (post-debridement) complying with the following requirements of the Margolis Predictive Score Baseline Wound Area and Wound Duration:

   1. 1(a) 2.5 cm2 to not-more-than 5 cm2 and not-less-than 6 months or;
   2. 1(b) Not-less-than 5 cm2 to not-more-than 15 cm2 and not-more-than 6 months
7. Ulcer with a clean, granulating base free of adherent slough at the T1 visit (post-debridement).
8. Female patients of childbearing potential, willing to use acceptable methods of contraception (birth control pills, barriers, or sexual abstinence). A urine pregnancy test must be performed, and negative at the T1 visit.
9. Patient able to understand the study procedures and willing to participate in the clinical study and able to comply with study visit schedule.
10. Provide signed informed consent.

Exclusion Criteria

1. Ulcer(s) deemed by the Investigator to be caused by a medical condition other than venous insufficiency. These may include, but are not limited to: fungal ulcerations, malignant ulcerations, diabetic (neuropathic) ulcerations, and ulcerations due to arterial insufficiency.
2. Increase or decrease by >30% in the study ulcer surface area at the T1 visit post-debridement as compared to the S1 visit study ulcer surface area post-debridement.
3. Ulcer exhibits clinical signs and symptoms of infection at S1to T1 in which case infection should be treated and the patient may after treatment be re-assessed for eligibility to enter into the study.
4. Known allergy to any of the protocol-stipulated treatment procedures, or non-tolerance of multi-layer compression therapy.
5. Ulcer which has undergone continuing high level of compression therapy for ≥12 months
6. Ulcer, which in the opinion of the Investigator is suspicious for cancer.
7. A history of more than 2 weeks' treatment with immunosuppressants (including systemic corticosteroids), cytotoxic chemotherapy, or application of topical steroids to the ulcer surface within one month prior to initial screening, or treatments with such medications during the screening period, or anticipated requirement of such medications during the course of the study.
8. IGF-1 treatment or treatment with a product containing IGF-1.
9. Treatment with Pentoxifylline (Trental®) within 30-days of S1 visit.
10. Treatment with any investigational drug(s) or therapeutic device(s) within 30 days preceding screening (i.e., S1); or anticipated (patient or physician anticipates) use of any of these therapies during the course of the study.
11. Malignant disease not in remission for 5 years or more, other than basal cell carcinoma, squamous cell carcinoma of the skin or cervical carcinoma in situ, that have been successfully treated without evidence of recurrence or metastases.
12. History of radiation at the ulcer site.
13. As determined by medical history, presence of one or more medical conditions including renal, hepatic, hematologic, active auto-immune or immune diseases that, in the opinion of the Investigator, would make the patient an inappropriate candidate for this ulcer healing study.
14. Known history of having Acquired Immunodeficiency Syndrome (AIDS) or with a history of known infection with Human Immunodeficiency Virus (HIV).
15. Previous participation in any VF001-DP study within the past 6 months.
16. Ulcer has been previously treated with tissue engineered materials (e.g., Apligraf® or Dermagraft®) or other scaffold materials (e.g., Oasis®, Matristem®) within the last 30 days prior to S1.
17. Ulcer which in the opinion of the Investigator might require negative pressure ulcer therapy or hyperbaric oxygen during the course of the study.

18. New York Heart Association Class III and IV congestive heart failure, as defined by the following criteria:

    1. Class III: Symptoms with moderate exertion
    2. Class IV: Symptoms at rest
19. Uncontrolled diabetes mellitus, defined as Hemoglobin A1C >10% confirmed by the Investigator.
20. Ulcer on the dorsum of the foot or with more than 50% of the ulcer below the malleolus is excluded.
21. Known history of acromegaly.
22. Any other medical or psychological condition (including relevant laboratory abnormalities at screening) that, in the opinion of the Investigator, may suggest a new and/or insufficiently understood disease, may present an unreasonable risk to the study patient as a result of his/her participation in this clinical trial, may make patient's participation unreliable, or may interfere with study assessments. The specific justification for patients excluded under this criterion will be noted in study documents (chart notes, CRFs, etc).
23. Women unwilling to use adequate birth control, if of reproductive potential and sexually active. Adequate birth control is defined as agreement to consistently practice an effective and accepted method of contraception throughout the duration of the study.
24. Pregnancy or breast-feeding.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Quadruple

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Placebo Comparator: Placebo plus Standard Care	Biological: Placebo; Placebo
Experimental: VF001-DP LD plus Standard Care; VF001-DP (14 micrograms per treatment) and Standard Care (low dose [LD])	Biological: VF001-DP LD; VF001-DP contains parts of normal vitronectin and Insulin-like growth factor 1 (IGF-I) combined in a single protein.
Experimental: VF001-DP HD plus Standard Care; VF001-DP (140 micrograms per treatment) and Standard Care (high dose [HD])	Biological: VF001-DP HD; VF001-DP contains parts of normal vitronectin and Insulin-like growth factor 1 (IGF-I) combined in a single protein.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
The percentage reduction in the study ulcer area in each treatment group over the 12-week Treatment Phase.	Patient's ulcers healing rate	12-weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
The proportion of patients with complete study ulcer closure within the 12-week Treatment Phase	How many patient's ulcers healed?	12-weeks
Time to complete study ulcer closure within the 12-week Treatment Phase	Time to Ulcer Healing	12-weeks
Time to first instance of no study ulcer pain (i.e., pain score less than 5 mm on Visual Analog Scale [VAS]) within the 12-week Treatment Phase	Measure of pain reduction to no pain	12-weeks
Time to clinically meaningful study ulcer pain reduction (33% reduction on VAS) within the 12-week Treatment Phase	Measure of meaningful pain reduction	12-weeks
Change in Quality-of-Life metrics Euro Quality-of-Life Questionnaire EQ-5D-5L	Quality of life	Up to 24-weeks
Change in Quality-of-Life metrics Patient Benefit Index - wound version PBI-W	Quality of life - specific to chronic wounds	Up to 24-weeks

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
The incidence of adverse events (AEs), including overall AEs, AEs related to the IP and study-ulcer-associated AEs.	Safety	Up to 24-weeks

Collaborators and Investigators

• Sponsor: Factor Therapeutics Ltd.
• Collaborators: Parexel; ARANZ Medical; Almac Clinical Services LLC
• Investigators: Principal Investigator: William Marston, MD, UNC-Chapel Hill

Study record dates

Study Major Dates

• Study Start (Actual): November 1, 2016
• Primary Completion (Anticipated): November 1, 2018
• Study Completion (Anticipated): February 1, 2019

Study Registration Dates

• First Submitted: November 7, 2016
• First Submitted That Met QC Criteria: November 23, 2016
• First Posted (Estimate): November 25, 2016

Study Record Updates

• Last Update Posted (Actual): September 25, 2018
• Last Update Submitted That Met QC Criteria: September 24, 2018
• Last Verified: September 1, 2018

More Information

Terms related to this study

• Keywords: Chronic Venous Leg Ulcer
• Additional Relevant MeSH Terms: Varicose Veins; Cardiovascular Diseases; Ulcer; Vascular Diseases; Skin Diseases; Leg Ulcer; Varicose Ulcer; Pathologic Processes; Skin Ulcer
• Other Study ID Numbers: VF00102

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: Yes