Topical PluroGel N for the Treatment of Mildly Infected Diabetic Foot Ulcers

Infection Clinical Trial

Official title:

Randomized, Double-blind, Vehicle-controlled 2-Arm Trial of Topical PluroGel N for the Treatment of Patients With Mildly Infected Diabetic Foot Ulcer CLINICAL PROTOCOL PGN-1300

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02091596
• Other study ID #: PGN-1300
• Secondary ID: D11AC00020
• Status: Completed
• Phase: Phase 2
• First received: March 12, 2014
• Last updated: September 24, 2014
• Start date: October 2013
• Est. completion date: September 2014

Study information

• Verified date: September 2014
• Source: PluroGen Therapeutics, Inc
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This will be a randomized, double-blind (evaluator-blind), vehicle-controlled study of 50 enrolled subjects. Adult subjects (greater than 18 years old) who present with a mildly infected diabetic foot ulcer (IDSA criteria) having full thickness (i.e., through the dermis but not involving joint capsule, tendon, and bone). Subjects must also provide informed consent and meet all other entry criteria to be enrolled and randomly assigned to receive PluroGel N or PluroGel vehicle.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 42
• Est. completion date: September 2014
• Est. primary completion date: September 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Non-hospitalized subjects with Type 1 or Type 2 diabetes mellitus as defined by the American Diabetes Association diagnostic criteria (ADA, 2010). Diabetes may be treated with insulin, oral hypoglycemic agents, diet, or a combination of these therapies. Subjects whose diabetes is considered "controlled" by diet or medication in the opinion of the physician.

• Males or females at least 18 years old.

• Subjects must be considered by the investigator to be reliable, willing and able to give signed informed consent, and must sign the informed consent form.

• Subjects must have a full thickness (i.e., extending through dermis but not involving tendon, bone, or joint capsule) ulcer on the foot distal to the malleoli with a surface area =1 cm2 after the wound has undergone appropriate debridement. Subjects must have localized mild infection of the ulcer, as defined by the IDSA criteria as per Appendix C, with in the PGN1300 Protocol, which the investigator believes would ordinarily be treated on an outpatient basis.

IDSA mild infection of an ulcer is defined as:

The presence of =2 of the following items:

• Local swelling or induration

• Erythema

• Local tenderness or pain

• Local warmth

• Purulent discharge (thick, opaque to white or sanguineous secretion) Local infection involving only the skin and the subcutaneous tissue. If erythema, must be >0.5 cm to =2 cm around the ulcer.

• Diabetic Foot Infection-General Parameters Score of at least 2 must be obtained in order to be eligible for enrollment.

• Diabetic Foot Infection-Wound Size Score of at least 1 must be obtained in order to be eligible for enrollment.

• The diagnosis of mild infection must be confirmed immediately following the Day 0 (Enrollment Visit) debridement, although pre-debridement purulence is to be counted as one manifestation of infection.

Exclusion Criteria:

• Subjects with IDSA-defined moderate infection as per Appendix C, including cellulitis extending > 2 cm; lymphangitis; spread beneath the fascia; deep tissue abscess; osteomyelitis; gangrene; muscle, joint, or bone involvement.

• Subjects with IDSA-defined severe infection as per Appendix C, within PGN1300 Protocol including systemic toxicity or metabolic instability (e.g., fever, chills, tachycardia, hypotension, confusion, vomiting, leukocytosis, acidosis, hyperglycemia, or azotemia).

• Subjects with systemic inflammatory response signs, as manifested by =2 of the following :

• Temperature >38°C or <36°C

• Heart rate >90 beats/min

• Respiratory rate >20 breaths/min or PaCO2 <32 mm Hg

• White blood cell count >12 000 or <4000 cells/µL or =10% immature (band) forms

• Subjects with local wound complications (e.g., prosthetic materials).

• Subjects currently receiving antibiotic treatment for a localized infection of the study ulcer and whose infection is improving in response to treatment.

• Subjects requiring concurrent systemic antimicrobials during the study period for any infection, including diabetic foot ulcer.

• Subjects in whom bone or joint involvement is suspected based on clinical examination (e.g., bone noted visually or by probing) or plain view X-ray.

• Subjects with clinically significant peripheral arterial disease requiring vascular reconstructive surgery. Subjects who are expected to be unable to care for their ulcer because of hospitalization, vacation, disability, etc. during the study period, or are unable to safely monitor the infection status at home.

• Subjects with known active alcohol or substance abuse within the 6 months preceding study entry.

• Subjects who are receiving immunosuppressive agents (other than corticosteroids), radiation therapy, or cytotoxic agents.

• Subjects who require treatment for a primary or metastatic malignancy (other than squamous or basal cell carcinoma of the skin).

• Subjects with a systemically immunocompromising disease, such as acquired immune deficiency syndrome or known human immunodeficiency virus infection.

• Subjects who have had an unexplained fever or chills during the week prior to enrollment.

• Subjects with other conditions considered by the investigator to be reasons for disqualification that may jeopardize subject safety or interfere with the objectives of the trial (e.g., acute illness or exacerbation of chronic illness, lack of motivation, history of poor compliance).

• Subjects with any known allergy or other contraindication to any ingredients in the study products.

• Women who are breast feeding, pregnant, or not using contraception unless sterile.

• Subjects who have been taking or expect to be taking any other investigational therapy within the 30 days prior to entry or during enrollment.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Diabetic Foot
• Diabetic Foot Ulcer
• Foot Ulcer
• Infection
• Ulcer

Intervention

Drug:
• PluroGel N
Study Drug
• PluroGel
PluroGel Vehicle Placebo Comparator

Locations

Country	Name	City	State
United States	AllCare Foot & Ankle, PA	Arlington	Texas
United States	Weil Foot & Ankle Institute	Des Plaines	Illinois
United States	ASAP Urgent-Care	Hamden	Connecticut
United States	Foot & Ankle Clinic	Los Angeles	California
United States	Advance Medical Research Center	Miami	Florida
United States	Med Research of Florida, LCC	Miami	Florida
United States	Miami Center for Clinical Research, LLC	Miami	Florida
United States	Phoenix Medical Research, LLC	Miami	Florida
United States	Unlimited Medical Research, LLC	Miami	Florida
United States	Sweet Hope Research Specialty, Inc.	Miami Lakes	Florida
United States	Samuel Merritt University	Oakland	California
United States	Research Integrity	Owensboro	Kentucky
United States	Paddington Testing Company, Inc	Philadelphia	Pennsylvania
United States	Ledesma Foot and Ankle	Phoenix	Arizona
United States	Coastal Podiatry Group	Virginia Beach	Virginia

Sponsors (2)

Lead Sponsor	Collaborator
PluroGen Therapeutics, Inc	Arkios BioDevelopment International

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical Response	Clinical Response is defined by the investigator's evaluation of the signs and symptoms of clinical infection.	14 Days	No