Clinical Drug Experience Knowledgebase

Criteria

Inclusion Criteria:

Able to understand and willing to sign the ICF.
Male or female subject ≥ 18 years.
Histologically/cytologically confirmed, locally advanced unresectable or metastatic solid tumors that are refractory to standard therapy, or for which no standard therapy exists.
Subject has measurable disease per RECIST v1.1.
ECOG Performance Status 0 to 1
Subjects with life expectancy of ≥ 3 month
No herbal/alternative medications prior to the first dose
Must have adequate hematological, hepatic and renal function as defined in the protocol.
Prior anti-tumor therapies of different kinds must have stopped before the first dose as defined by protocol
Effective contraception for both male and female subjects if the risk of conception exists

Exclusion Criteria:

Pregnant or nursing females.
Any remaining AEs > grade 1 from prior anti-tumor treatment as per CTCAE v4. 03, with exception of the residual hair loss;
Received a biologic G-CSF, GM-CSF or erythropoietin within 14 days prior to the first dose of study drug;
Subjects who had prior treatment with an anti-PD-L1 product
History of documented autoimmune disease except for autoimmune hypothyroidism and well-controlled Type 1 diabetes mellitus.
W/o autoimmune condition requiring systemic treatment with immunosuppressive medications within 14 days before the planned first dose of study drug.
Primacy central nervous system (CNS) malignancy or symptomatic CNS metastases are not allowed, with exceptions defined in protocol.
Major surgery within the 28-days from the screening
Subjects with idiopathic pulmonary fibrosis or unresolved active or chronic inflammatory pulmonary disease are excluded.
History of human immunodeficiency virus (HIV) infection, active hepatitis B or C. HBV carriers
History of primary immunodeficiency, stem cell or organ transplant, or previous clinical diagnosis of tuberculosis disease.
Clinically significant acute infections 4 weeks and any infection 2 weeks prior to the first dose administration.
Known allergies, hypersensitivity, or intolerance to protein-based therapies or with a history of any significant drug allergy
Subjects who experienced immunotherapy-related adverse events (irAE) grade ≥ 3, or who had to discontinue prior anti-PD-1 treatment due to irAEs of any grade.
Severe or uncontrolled cardiac disease requiring treatment as defined in protocol
Any other serious underlying medical, psychiatric, psychological, familial or geographical condition that, in the judgment of the investigator, might impair the subject's benefit from the trial treatment
Known history of hypersensitivity to any components of the MSB2311 product.