New skin patch could speed recovery after skin cancer removal

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * The potential subject must be at least 18 years of age or older. * The potential subject must have undergone Mohs micrographic surgery for a cutaneous malignancy (e.g., basal cell carcinoma, or squamous cell carcinoma). * The potential subject must have a post-Mohs surgical defect that is suitable for treatment with a CAMP product or healing by secondary intention. * The surgical site has received standard Mohs excision and hemostasis with no requirement for immediate flap or graft reconstruction as determined by the treating surgeon. * If the surgical defect is on the lower extremity, the limb must have adequate perfusion confirmed by vascular assessment. Any of the following methods performed within 3 months of the first screening visit are acceptable: 1. Ankle-Brachial Index (ABI) between 0.7 and ≤ 1.3; 2. Toe-Brachial Index (TBI) ≥ 0.6; 3. Transcutaneous Oxygen Measurement (TCOM) ≥ 40 mmHg; 4. Pulse Volume Recording (PVR): biphasic. * If the subject has multiple Mohs defects, they must be separated by at least 2 cm. The largest defect satisfying the inclusion and exclusion criteria will be designated as the target wound. * The potential subject must agree to attend the weekly study visits required by the protocol. * The potential subject must be willing and able to participate in the informed consent process. Exclusion Criteria: * The potential subject is known to have a life expectancy of \< 6 months. * The potential subject's target wound is not secondary to a Mohs excision. - -. The target wound is infected or there is cellulitis in the surrounding skin. * The target wound: 1. Exposes tendon, bone, or joint space, and/or\[MM6.1\]\[RB6.2\] 2. Requires immediate complex flap or graft reconstruction in the judgment of the surgeon. * The potential subject has participated in a clinical trial involving treatment with an investigational product within the previous 30 days. * The potential subject has glycated hemoglobin (HbA1c) greater than 10% within 3 months of the initial screening visit. * The potential subject, in the opinion of the investigator, has a medical or psychological condition that may interfere with study assessments.