Clinical Trial Finder

Inclusion Criteria:

• - Signed Informed Consent Form and the subject's ability to follow the Protocol requirements; - Age: 18 years and older at the signing of the informed consent; - Histologically confirmed metastatic solid malignant tumors (non-small cell lung cancer, renal cell carcinoma, melanoma), refractory or recurrent after one or more courses of previous therapy and not subject to surgical treatment and radiation therapy.

• - regardless of the presence and success of previous treatment; - ECOG performance status ≤ 2; - At least one RESICT 1.1-defined measurable target lesion; - Completion of the previous drug treatment of the underlying disease (if applicable) at least 28 days before the first administration of GNR-051; - Resolution or stabilization of toxicity manifestations of previous radiation or chemotherapy.

Exclusion Criteria:

• - Prior treatment with anti-CTLA4 and/or anti-PD-1/PD-L1/PD-L2 agents; - Hypersensitivity to any of the components of GNR-051; - Progression (growth of previous, appearance of new) metastases in the brain and meninges, identified by CT or MRI, in a period of less than 56 days before the first administration of GNR-051; worsening of neurological symptoms in a patient with metastases in the brain or meninges within a period of less than 28 days before the first administration of GNR-051; or continued treatment of metastases in the brain or meninges with glucocorticosteroids (GCS) for a period of less than 14 days before the first administration of GNR-051 (except for a maintenance daily dose of GCS equivalent to 10 mg of prednisolone); - Inability to conduct a biopsy according to the protocol; - Left ventricular ejection fraction (LVEF) <50% (EchoCG); - The need to use anticancer drugs, other than the investigated one, for at least 3 months after the first administration of the drug; - Patients who need radiotherapy or surgical therapy; - Previous radiotherapy ended <28 days before the first dose administration; - Previous stereotactic radiation therapy ended <14 days before the first dose administration; - Therapeutic use of radiopharmaceuticals ≤56 days prior to first dose administration; - Patients who have received another experimental drug (not registered in Russia) within 28 days or 5 half-lives of the experimental drug before the first administration GNR-051; - Patients who have received vaccines against infectious diseases (eg influenza virus) within 28 days before the first administration of the drug; - Patients who have received narcotic analgesics <14 days before the first administration of GNR-051; - Surgery with general anesthesia <28 days before the first administration of GNR-051.

• - Surgery with regional / epidural anesthesia <72 hours and / or not all post-anesthetic AEs resolved before the first administration of GNR-051; - Laboratory parameters: - Absolute leukocyte count <2000 / μL; - Absolute neutrophil count <1500 / μL; - Absolute platelet count <100 × 103 / μL; - Hemoglobin level <9.0 g / dL; - Creatinine> 2 mg / dL; - AST> 2.5 × the upper limit of normal (ULN) in the absence of liver metastases, or> 5 × ULN with the liver metastases; - ALT > 2.5 × ULN in the absence of liver metastases, or> 5 × ULN with the liver metastases; - Total bilirubin> 2 × ULN; - Systemic autoimmune diseases (including but not limited to SLE, Crohn's disease, ulcerative colitis, systemic scleroderma, inflammatory myopathy, mixed connective tissue disease, overlap syndrome, etc.); - Concomitant cancer (except for basal or squamous cell carcinoma of the skin, superficial bladder cancer, carcinoma in situ of the cervix, prostate, or breast); - Patients who need therapy with corticosteroids or other immunosuppressants; - Systemic therapy with corticosteroids or immunosuppressants for ≤7 days before the first administration GNR-051; - Any other concomitant condition (e.g., medical condition, mental disorders, alcohol/drug abuse) that constitutes an unacceptable risk to the patient's health during the investigational therapy or prevents a patient from following the Protocol procedures; - Active HBV/HCV/HIV infection; - Pregnant or lactating female; - Patients with reproductive potential who do not agree to practice acceptable methods of birth control throughout the entire trial period, starting from signing the informed consent and up to 6 months after the last dose of GNR-051; - Simultaneous participation in other clinical trials.

GNR-051 is a monoclonal antibody, targeting the Programmed Death-1 (PD-1) membrane receptor on T lymphocytes and other cells of the immune system. The anti-PD-1 antibody, preventing the binding of the PD-1 receptor with the ligands PD-L1 and PD-L2, reactivates the pool of tumor-specific cytotoxic T-lymphocytes in the tumor microenvironment and, thus, reactivates the antitumor immunity. GNR-051 is able to block the signaling molecule PD-1, which suppresses the antitumor immune response, for the treatment of cancer.

Arms

Interventions