This study is evaluating the safety, side effects, how the body processes HH160, and its early anticancer activity when given alone or with other cancer treatments in participants with advanced solid tumors. The study will also identify the recommended dose for future studies. The trial includes two phases and is expected to last about 4 years, with treatment and follow-up lasting approximately 6-12 months each.
Adults aged 18 to 75 years with signed informed consent.
Histologically or cytologically confirmed advanced solid tumors meeting phase-specific disease requirements.
At least 1 measurable lesion per RECIST v1.1.
Eastern Cooperative Oncology Group Performance Status (ECOG) Performance Status of 0 or 1 with life expectancy ≥ 12 weeks.
Active leptomeningeal disease or uncontrolled/untreated brain metastases.
History of severe hypersensitivity reactions to monoclonal antibodies, bispecific antibodies, trispecific antibodies, or study drug components.
Other malignancy within 3 years prior to first dose, except specified curatively treated cancers.
Uncontrolled pleural effusion, pericardial effusion, or ascites requiring frequent drainage.
Huahui Health
Lead sponsor
BeOne Medicines
Collaborator