About this trial
The goal of this study is to learn if BC008-1A given 900mg or 1200mg intravenously once every 3 weeks is safe and effective to treat patients with advanced esophageal cancer or advanced non-small cell lung cancer. It will also learn about the safety and pharmacokinetics of BC008-1A.
Eligibility criteria
Qualifiers
Sign a written informed consent form before any study-specific procedures and be able to follow the visit schedules and related procedures stipulated in the protocol.
Male or female patients aged ≥ 18 years old.
Expected survival time ≥ 12 weeks.
According to the Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1), there should be at least one measurable tumor lesion shown by CT or MRI examination (lesions that have not received radiotherapy before). If a lesion located in the irradiated area that has received radiotherapy previously clearly shows progression meeting the RECIST 1.1 criteria, such lesion can be regarded as a measurable lesion.
Disqualifiers
Having been previously exposed to any anti-TIGIT drugs.
Currently participating in another interventional clinical study, except for participation in observational (non-interventional) clinical studies or being in the survival follow-up stage of an interventional study.
Having received any investigational drugs within 4 weeks prior to the first administration of the study drug.
Having an autoimmune disease or a history of autoimmune diseases or related symptoms.
Trial design
Treatments tested in this trial
- BC008-1A 900mg
- BC008-1A 1200mg
Treatment groups
Sponsors and collaborators
Sichuan Luzhou Buchang Biopharmaceutical Co., Ltd.
Lead sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Collaborator