Trial of TRX518 (Anti-GITR mAb) in Stage III or IV Malignant Melanoma or Other Solid Tumors (TRX518-001)

This is an interventional treatment trial for Unresectable Stage III or Stage IV Malignant Melanoma or Other Solid Tumor Malignancies focused on measuring Malignant melanoma, Metastatic, Unresectable, Stage III or Stage IV, Solid tumor Read More

Inclusion Criteria (Parts B & C):

• 18 years or older
• Histologically confirmed unresectable Stage III or Stage IV malignant melanoma, or other solid tumor malignancies
• Failed to respond to or relapsed following standard treatment, declined or was not eligible for standard treatment.
• Expected survival of at least 12 weeks.
• Eastern Cooperative Oncology Group performance status score of 0 or 1 is required.
• Evidence of adequate organ function by standard laboratory tests.

Exclusion Criteria (Parts B & C):

• Evidence of progression of central nervous system (CNS) metastases or symptomatic CNS metastases within 35 days prior to dosing.
• Ocular melanoma which has not metastasized or presence of a non-solid tumor.
• A history of any major surgery within 4 weeks prior to dosing.
• Any history of antitumor therapy completed within 28 days prior to dosing.
• Subjects with active autoimmune disease or history of known or suspected autoimmune disease, with the exception of subjects with isolated vitiligo, resolved childhood asthma/atopy, psoriasis not requiring systemic treatment and controlled thyroid disorders.
• Clinically significant heart disease, defined as NYHA Class III or IV.
• Any significant systemic infection requiring IV antibiotics.
• Known to be human immunodeficiency virus (HIV) positive, have hepatitis B surface antigen (HBsAg), or hepatitis C antibodies (HCAb) unless HCV RNA undetected/negative.
• Treatment with any other anti-human GITR monoclonal antibody (mAb) or immunomodulatory therapy 42 days prior to dosing (30 days for Interleukin-2 & Interferon-α, 7 days for Topical Imiquimod).
• Adverse events from prior anti-cancer therapy that have not resolved to grade ≤1 except for alopecia, vitiligo, or endocrinopathy managed with replacement therapy.
• Use of any investigational drugs within 30 days prior to dosing.
• Any condition that requires or is likely to require treatment with pharmacologic doses of systemic corticosteroids. Subjects are permitted to receive physiologic replacement of corticosteroid therapy (≤ 10 mg prednisone daily).