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Phase 2 Randomized Study to Compare Ultrasonic Drug Delivery to Standard of Care for the Treatment of Infections in Non-Healing Wounds

Primary Purpose

Acute Bacterial Skin and Skin Structure Infection (ABSSSI), Non-healing Wound

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Ultrasonic Drug Delivery
Standard of Care Antibiotic Treatment
Sponsored by
Sonescence, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Bacterial Skin and Skin Structure Infection (ABSSSI)

Eligibility Criteria

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

Inclusion Criteria:

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Must have a non-healing wound which shows clinical signs of infection characterized by erythema and at least two of the following signs of infection: Induration/swelling; Purulent drainage/discharge; Fluctuance; Heat/localized warmth; Tenderness/pain to palpation
  • Patient must have one (1) or more of the following confirmed infection types of the lower extremity: a) Cellulitis/erysipelas: A diffuse skin infection characterized by spreading areas of redness, edema, and/or induration; b) Wound infection: An infection characterized by purulent drainage from a wound with surrounding redness, edema, and/or induration; c) Major cutaneous abscess: An infection characterized by a collection of pus within the dermis or deeper that is accompanied by redness, edema, and/or induration
  • A minimum affected area that involves: At least 75cm2 of erythema; and is defined by a margin of erythema in at least one (1) direction that is ≥ 5 cm from the edge of the wound.
  • In addition to the requirement for erythema, all patients are required to have at least two (2) of the following signs of acute bacterial skin and skin structure infection (ABSSSI): a) Purulent drainage/discharge; b) Fluctuance; c) Heat/localized warmth; d) Tenderness to palpation; and e) Swelling/induration
  • Patients must present with at least ONE (1) of the following systemic signs of infection: a) An elevated body temperature ≥ 100.4 Fahrenheit as measured by clinical staff or investigator within 24 hours of baseline at screening; and/or b) White blood cell count > 12,000 cells/mm3; c) manually performed white blood differential count with ≥ 10% band forms, regardless of peripheral white blood cell count.
  • Bacteria culture positive for gram positive bacteria.
  • Ability and willingness to accept subcutaneous administration of antibiotic and local anesthesia.
  • For females of reproductive potential: use of highly effective contraception and agreement to use such a method during study participation.
  • Agreement to adhere to the study intervention regimen.

Exclusion Criteria:

  • Patients with conditions that would alter the interpretation of a primary endpoint, including: patients with neutropenia; and/or patients with peripheral neuropathy
  • Participation in another study of an investigational drug or device within 30 days prior to administration of investigational treatment.
  • Pregnant or lactating women.
  • Patients with a known allergic reaction or hypersensitivity to cefazolin or penicillin.
  • Infections caused exclusively by gram-negative bacteria (without gram-positive bacteria present) and infections caused by fungi, whether alone or in combination with a bacterial pathogen.
  • Presence of gram-negative bacteremia, even in the presence of gram-positive infection or gram-positive bacteremia.
  • Patients with evidence of meningitis, gas gangrene, gangrene, septic arthritis, or osteomyelitis, endovascular infection, such as clinical and/or echocardiographic evidence of endocarditis or septic thrombophlebitis.
  • Infections involving a diabetic foot ulceration, perirectal abscess or a decubitus ulcer.
  • Patients with an infection involving a limb with evidence of critical ischemia of an affected limb defined as any of the following criteria: absent or abnormal Doppler wave forms, toe blood pressure of <45 mm Hg, ankle brachial index <0.4, critical ischemia as assessed by a vascular surgeon.
  • Patient with an infected device.
  • Suspicion of skin cancer at the wound site (i.e., clinical evaluation is currently on-going).
  • Patients who have a history of clinically significant or uncontrolled cardiac disease, including congestive heart failure, angina, myocardial infarction, arrhythmia, including New York Heart Association (NYHA) functional classification of III (marked limitation of physical activity comfortable at rest but less than ordinary activity results in fatigue, palpitation or dyspnoea) or Class IV (unable to carry out any physical activity without discomfort - symptoms at rest. If any physical activity is undertaken, discomfort is increased).
  • Patients who have any other life-threatening illness or organ system dysfunction, which, in the opinion of the Investigator, would either compromise patient safety or interfere with the evaluation of the safety of the test drug.
  • Anticipated need of antibiotic therapy for longer than 14 days.
  • Medical conditions in which chronic inflammation may preclude assessment of clinical response to therapy even after successful treatment (e.g., chronic stasis dermatitis of the lower extremity).
  • Known or suspected human immunodeficiency virus (HIV) infected patients with a CD4 (cluster of differentiation 4) cell count < 200 cells/mm3 or with a past or current acquired immunodeficiency syndrome (AIDS) - defining condition and unknown CD4 count.
  • Patients with a recent bone marrow transplant.
  • Patients receiving oral steroids > 20 mg prednisone per day (or equivalent) or receiving immunosuppressant drugs after organ transplantation.
  • Patients with a rapidly fatal illness who are not expected to survive for three months.
  • Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the patient inappropriate for entry into this study.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Investigational Group

    Comparator Group

    Arm Description

    Patients who are randomized to the investigational regimen will receive Ultrasonic Drug Delivery, which includes infusion of up to 2 grams of cefazolin in 100 mL saline followed by external ultrasound in addition to standard of care antibiotic treatment according to the antibiotic package insert instructions for the particular gram-positive pathogen over a period of no more than 14 days as well as standard of care adjunct therapy.

    Patients who are randomized to the comparator regimen will receive antibiotic according to the antibiotic package insert instructions for standard of care for the particular gram-positive pathogen over a period of no more than 14 days as well as standard of care adjunct therapy.

    Outcomes

    Primary Outcome Measures

    Wound healing and eligibility for grafting
    Number of wounds 100% granulation/ready to graft as assessed by a blinded observer
    Reduction or elimination of pain
    Pain assessed by participant questionnaire

    Secondary Outcome Measures

    Clinical signs and symptoms of infection will be assessed
    Eradication of infection; percent of wound closure

    Full Information

    First Posted
    October 25, 2018
    Last Updated
    November 4, 2018
    Sponsor
    Sonescence, Inc.
    Collaborators
    University of Southern California
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03732365
    Brief Title
    Phase 2 Randomized Study to Compare Ultrasonic Drug Delivery to Standard of Care for the Treatment of Infections in Non-Healing Wounds
    Official Title
    A Phase 2 Randomized Study to Compare the Efficacy and Safety of Ultrasonic Drug Delivery to Standard of Care for the Treatment of Acute Bacterial Skin and Skin Structure Infections in Chronic Non-Healing Wounds
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    February 1, 2019 (Anticipated)
    Primary Completion Date
    January 31, 2020 (Anticipated)
    Study Completion Date
    July 31, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Sonescence, Inc.
    Collaborators
    University of Southern California

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    Yes
    Studies a U.S. FDA-regulated Device Product
    Yes
    Device Product Not Approved or Cleared by U.S. FDA
    Yes
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    This is a randomized study to compare the safety and efficacy of a single dose of up to 2 grams of cefazolin administered using a new drug delivery method called Ultrasonic Drug Delivery (UDD), combined with standard of care (SOC) antibiotic therapy, oral or IV, compared to standard of care (SOC) antibiotic therapy alone, in treating chronic wounds with skin and soft tissue infection, containing gram-positive pathogens, in lower extremities.
    Detailed Description
    This is a Phase 2, single-center, parallel-group study to compare the efficacy and safety of UDD plus standard of care (SOC) with SOC alone for the treatment of skin and soft tissue infections in non-healing wounds. After review of screening results to determine eligibility, a patient will be randomly assigned to one of the two treatments: Investigational Group: This group will receive administration of a single dose of cefazolin, using a novel new drug delivery system called Ultrasonic Drug Delivery (UDD), to the site of infection, combined with SOC, followed by best available adjunct therapy. An optional two additional treatments will be available if needed. Comparator Group: This group will receive conventional standard of care treatment followed by best available adjunct therapy. Efficacy will be assessed by clinical response based on the presence of vascularized granulation tissue, reduction of pain, temperature, measurement of lesion size and temperature, culture and gram stain results, and clinical signs of infection (erythema, induration/swelling, fluctuance, purulent drainage, warmth/localized heat, and tenderness/pain). Additionally, efficacy will be assessed by resolution of infection and microbiological assessments. Safety will be assessed by reported adverse events, clinical laboratory tests (hematology, serum chemistry, fasting glucose, hs-CRP), and concomitant medication.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Acute Bacterial Skin and Skin Structure Infection (ABSSSI), Non-healing Wound

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Model Description
    Single-center, parallel-group study to compare the efficacy and safety of UDD plus standard of care with standard of care alone for the treatment of skin and soft tissue infections in chronic non-healing wounds.
    Masking
    Outcomes Assessor
    Masking Description
    This study will be observer-blinded. Each investigational site will be required to have a Sponsor-approved plan (a site-specific Blinding Plan) that describes site-specific precautions being taken to ensure that the study is observer-blinded, taking into account the specific subject care procedures, equipment, and information accessibility at that site. At each investigational site, at least 1 blinded investigator (referred to as "Blinded Observer") will not know the subject's treatment assignment and will conduct clinical assessments (including efficacy and safety. The Blinded Observer will not ask other members of the study team, the subject, or the subject's parent(s)/legally acceptable representative(s) which study treatment is being given, and will avoid all attempts to uncover treatment assignment. The Blinded Observer will see the subject during times when study treatment is NOT being administered.
    Allocation
    Randomized
    Enrollment
    30 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Investigational Group
    Arm Type
    Experimental
    Arm Description
    Patients who are randomized to the investigational regimen will receive Ultrasonic Drug Delivery, which includes infusion of up to 2 grams of cefazolin in 100 mL saline followed by external ultrasound in addition to standard of care antibiotic treatment according to the antibiotic package insert instructions for the particular gram-positive pathogen over a period of no more than 14 days as well as standard of care adjunct therapy.
    Arm Title
    Comparator Group
    Arm Type
    Active Comparator
    Arm Description
    Patients who are randomized to the comparator regimen will receive antibiotic according to the antibiotic package insert instructions for standard of care for the particular gram-positive pathogen over a period of no more than 14 days as well as standard of care adjunct therapy.
    Intervention Type
    Combination Product
    Intervention Name(s)
    Ultrasonic Drug Delivery
    Other Intervention Name(s)
    Cefazolin with external ultrasound
    Intervention Description
    A maximum dose of 2 grams cefazolin in a solution of 1 gram/100 mL sterile saline will be injected into the affected area, followed by a 3-minute application of external ultrasound delivered at an acoustic intensity equal to 3 watts/square centimeter of surface area.
    Intervention Type
    Drug
    Intervention Name(s)
    Standard of Care Antibiotic Treatment
    Intervention Description
    Antibiotic treatment according to the antibiotic package insert instructions for the particular gram-positive pathogen over a period of no more than 14 days.
    Primary Outcome Measure Information:
    Title
    Wound healing and eligibility for grafting
    Description
    Number of wounds 100% granulation/ready to graft as assessed by a blinded observer
    Time Frame
    12 weeks
    Title
    Reduction or elimination of pain
    Description
    Pain assessed by participant questionnaire
    Time Frame
    12 weeks
    Secondary Outcome Measure Information:
    Title
    Clinical signs and symptoms of infection will be assessed
    Description
    Eradication of infection; percent of wound closure
    Time Frame
    Day 9 and Day 91

    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: Provision of signed and dated informed consent form Stated willingness to comply with all study procedures and availability for the duration of the study Must have a non-healing wound which shows clinical signs of infection characterized by erythema and at least two of the following signs of infection: Induration/swelling; Purulent drainage/discharge; Fluctuance; Heat/localized warmth; Tenderness/pain to palpation Patient must have one (1) or more of the following confirmed infection types of the lower extremity: a) Cellulitis/erysipelas: A diffuse skin infection characterized by spreading areas of redness, edema, and/or induration; b) Wound infection: An infection characterized by purulent drainage from a wound with surrounding redness, edema, and/or induration; c) Major cutaneous abscess: An infection characterized by a collection of pus within the dermis or deeper that is accompanied by redness, edema, and/or induration A minimum affected area that involves: At least 75cm2 of erythema; and is defined by a margin of erythema in at least one (1) direction that is ≥ 5 cm from the edge of the wound. In addition to the requirement for erythema, all patients are required to have at least two (2) of the following signs of acute bacterial skin and skin structure infection (ABSSSI): a) Purulent drainage/discharge; b) Fluctuance; c) Heat/localized warmth; d) Tenderness to palpation; and e) Swelling/induration Patients must present with at least ONE (1) of the following systemic signs of infection: a) An elevated body temperature ≥ 100.4 Fahrenheit as measured by clinical staff or investigator within 24 hours of baseline at screening; and/or b) White blood cell count > 12,000 cells/mm3; c) manually performed white blood differential count with ≥ 10% band forms, regardless of peripheral white blood cell count. Bacteria culture positive for gram positive bacteria. Ability and willingness to accept subcutaneous administration of antibiotic and local anesthesia. For females of reproductive potential: use of highly effective contraception and agreement to use such a method during study participation. Agreement to adhere to the study intervention regimen. Exclusion Criteria: Patients with conditions that would alter the interpretation of a primary endpoint, including: patients with neutropenia; and/or patients with peripheral neuropathy Participation in another study of an investigational drug or device within 30 days prior to administration of investigational treatment. Pregnant or lactating women. Patients with a known allergic reaction or hypersensitivity to cefazolin or penicillin. Infections caused exclusively by gram-negative bacteria (without gram-positive bacteria present) and infections caused by fungi, whether alone or in combination with a bacterial pathogen. Presence of gram-negative bacteremia, even in the presence of gram-positive infection or gram-positive bacteremia. Patients with evidence of meningitis, gas gangrene, gangrene, septic arthritis, or osteomyelitis, endovascular infection, such as clinical and/or echocardiographic evidence of endocarditis or septic thrombophlebitis. Infections involving a diabetic foot ulceration, perirectal abscess or a decubitus ulcer. Patients with an infection involving a limb with evidence of critical ischemia of an affected limb defined as any of the following criteria: absent or abnormal Doppler wave forms, toe blood pressure of <45 mm Hg, ankle brachial index <0.4, critical ischemia as assessed by a vascular surgeon. Patient with an infected device. Suspicion of skin cancer at the wound site (i.e., clinical evaluation is currently on-going). Patients who have a history of clinically significant or uncontrolled cardiac disease, including congestive heart failure, angina, myocardial infarction, arrhythmia, including New York Heart Association (NYHA) functional classification of III (marked limitation of physical activity comfortable at rest but less than ordinary activity results in fatigue, palpitation or dyspnoea) or Class IV (unable to carry out any physical activity without discomfort - symptoms at rest. If any physical activity is undertaken, discomfort is increased). Patients who have any other life-threatening illness or organ system dysfunction, which, in the opinion of the Investigator, would either compromise patient safety or interfere with the evaluation of the safety of the test drug. Anticipated need of antibiotic therapy for longer than 14 days. Medical conditions in which chronic inflammation may preclude assessment of clinical response to therapy even after successful treatment (e.g., chronic stasis dermatitis of the lower extremity). Known or suspected human immunodeficiency virus (HIV) infected patients with a CD4 (cluster of differentiation 4) cell count < 200 cells/mm3 or with a past or current acquired immunodeficiency syndrome (AIDS) - defining condition and unknown CD4 count. Patients with a recent bone marrow transplant. Patients receiving oral steroids > 20 mg prednisone per day (or equivalent) or receiving immunosuppressant drugs after organ transplantation. Patients with a rapidly fatal illness who are not expected to survive for three months. Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the patient inappropriate for entry into this study.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    David G Armstrong, Ph.D., DPM
    Phone
    (213) 740-2311
    Email
    armstrong@usa.net
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    David G Armstrong, Ph.D., DPM
    Organizational Affiliation
    University of Southern California
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Phase 2 Randomized Study to Compare Ultrasonic Drug Delivery to Standard of Care for the Treatment of Infections in Non-Healing Wounds

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