PriMatrix for the Management of Diabetic Foot Ulcers

Inclusion Criteria

Subjects are required to meet all of the following criteria for enrollment into the study and subsequent randomization:

• The subject has signed and dated an informed consent form.
• In the opinion of the investigator, subject is able and willing to comply with study procedures, including study visits, study dressing regimens and compliance with study required off-loading device.
• The subject is ≥ 18 years of age.
• The subject, if female of child-bearing potential, must not be pregnant. To document pregnancy status, subject statement is acceptable.
• The subject has Type I or Type II diabetes mellitus with investigator-confirmed glycosylated hemoglobin (HbA1c) of ≤ 12% within 3 months prior to screening visit.
• The subject has at least one diabetic foot ulcer that meets ALL of the following criteria:
• Ulcer which has been in existence for a minimum of two weeks, prior to signing the Informed Consent Form for trial participation.
• Ulcer is a partial or full thickness diabetic foot ulcer without capsule/tendon/bone exposure.
• Ulcer does not have tunneling, undermining, or sinus tracts that necessitates surgical OR debridement and/or penetrates to capsule/tendon/bone.
• Ulcer is located on the foot or ankle (with no portion above the top of the malleolus).
• Ulcer size (area) is > 1 cm2 and 50 mmHg at time of screening,
• TcPO2 > 40 mmHg at time of screening
• The subject or responsible caregiver is willing and able to maintain required applicable dressing changes as well as study required off-loading/protective device for the duration of the study.

Exclusion Criteria

Subjects will not be enrolled in the study if any of the following criteria are met:

• The subject was previously randomized and treated under this clinical study protocol.
• The subject has suspected or confirmed gangrene or ulcer infection of the study ulcer or receiving systemic antibiotics for the treatment of such.
• The subject has suspected or confirmed osteomyelitis of the foot with the study ulcer.
• The subject has a history of hypersensitivity to bovine collagen, as determined by prior medical history.

Protocol Number: T-PMXDFU-01 Confidential Page 23 of 64 Version 5.0 06 Nov 2018

• The subject has participated in another clinical trial involving a device or a systemically administered investigational study drug/treatment within 28 days of randomization.
• The subject has received, within 28 of signing Informed Consent Form, or is scheduled to receive during study participation, a medication or treatment which is known to interfere with or affect the rate and quality of ulcer healing (e.g., systemic steroids, immunosuppressive therapy, autoimmune disease therapy, dialysis, radiation therapy to the foot, vascular surgery, angioplasty, or thrombolysis).
• The subject has a history of bone cancer or metastatic disease of the affected limb, radiation therapy to the foot, or has had chemotherapy within the 12 months prior to signing Informed Consent Form for trial participation.
• In the opinion of the investigator, the subject has a history of, or is currently diagnosed with, any illness or condition, other than diabetes, that could interfere with ulcer healing (e.g., end-stage renal disease, severe malnutrition, liver disease, aplastic anemia, connective tissue disorder, acquired immune deficiency syndrome, HIV positive, or sickle cell anemia).
• In the opinion of the investigator, the subject has unstable Charcot foot or Charcot with bony prominence that could inhibit ulcer healing.
• The subject has ulcers secondary to a disease other than diabetes (e.g., vasculitis, neoplasms, or hematological disorders).
• In the opinion of the investigator, the subject has excessive lymphedema that could interfere with off-loading and/or ulcer healing.
• The study ulcer has received ulcer dressings that included growth factors, engineered tissues, or skin substitutes within 28 days of randomization or is scheduled to