Study of Topical SOR007 Ointment for Cutaneous Metastases

This is an interventional treatment trial for Cutaneous Metastasis focused on measuring cutaneous metastases, cutaneous metastasis, skin metastases, skin metastasis Read More

Inclusion Criteria:

1. Signed informed consent;
2. Male and female patients ≥ 18 years of age;
3. Malignancies resulting in cutaneous metastasis originating from: breast, lung, head and neck, pancreatic, urinary bladder, prostate, testicular, ovarian, uterine, cervical, gastric, adrenal, thyroid, parathyroid cancers, or other solid tumors;
4. Cutaneous metastases diagnosis confirmed prior to consent by preferred institutional methodology which may include, but is not limited to: biopsy; conventional radiography; imaging techniques to include bone scan (scintigraphy), computed tomography (CT), fluorodeoxyglucose-positron emission tomography (FDG-PET)/CT), magnetic resonance imaging (MRI), F-fluoromisonidazole-(F-FMISO) PET/CT, fluorothymidine-(FLT) PET/CT, fluoroestradiol-(FES) PET/CT, and PET/MRI;
5. ECOG Grade 0 - 2, with minimum life expectancy of at least 3 months;
6. At least one baseline eligible lesion. Per RECIST criteria (version 1.1), an eligible lesion at baseline is considered measurable when ≥ 10mm diameter in the longest diameter;
7. Willing to refrain from using lotions, creams, etc. during the treatment period;

8. Subjects with adequate organ and bone marrow function as defined below:

   • ANC ≥ 1,500/µl
   • Hemoglobin ≥ 9.5 grams/dL
   • Platelets ≥ 75,000/µl
   • AST (aspartate transaminase or SGOT)/ALT (alanine aminotransferase or SGPT) ≤ 3.0 x ULN and total bilirubin ≤ 2.0 x ULN with no evidence of cholestasis
   • Creatinine ≤ 1.5x ULN;
9. Last dose of any systemic non-taxane cytotoxic chemotherapy completed at least one day prior to Day 1. Last dose of any systemic taxane cytotoxic chemotherapy completed at least 4 weeks prior to Day 1
10. Willing to use appropriate birth control for patients of child-bearing potential;
11. Abstinence from all manner of physical contact near the treatment area during and up to 2 weeks after the treatment phase.

Exclusion Criteria:

1. Open or ulcerated wound(s) extending through the dermis within the treatment area;
2. Colorectal, hepatocellular, gallbladder, cholangiocarcinoma, neuroendocrine, melanomas, hematological and central nervous system (CNS) malignancies;
3. Active viral hepatitis A, B, or C or preexisting or acute liver disease;
4. Systemic treatment or localized treatment to target area with the following within the 4 weeks prior to the first treatment visit: radiotherapy, intralesional therapy; laser therapy surgery (other than biopsy), local hyperthermia, levulinic acid, 5-fluorouracil, high potency corticosteroids (including systemic steroids), retinoids, diclofenac, hyaluronic acid, imiquimod;
5. Elective surgery for treatment of the cutaneous metastases during the study and up to 4 weeks after the treatment period. Cutaneous metastases are required to remain in-situ and measurable for up to 2 weeks after last treatment to achieve study objectives;
6. Known allergic reactions, irritations or sensitivity to the active ingredients or other components of SOR007;
7. Symptoms of a clinically significant illness that may place the subject at risk by trial participation or influence the outcome of the trial in the four weeks before first treatment and during the trial;
8. Participation in the treatment phase of another clinical trial within the four weeks prior to treatment in this clinical trial;
9. Investigator's opinion of subject's probable noncompliance or inability to understand the trial and/or give adequate informed consent;
10. Evidence of current chronic alcohol or drug abuse;
11. Pregnancy and/or lactating.