Condition: Non-Small Cell Lung Cancer · Sponsor: Shanghai Hengrui Pharmaceutical Co., Ltd.
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This study is a multicenter, open-label, dose-finding/efficacy-expanding Phase IB/II clinical trial to evaluate SHR-A2102 in combination with adebelimab in combination with SHR-8068 in patients with locally advanced or metastatic non-small cell lung cancer. The study consists of two phases: Phase IB to explore the safety/tolerability of SHR-A2102 in combination with adebelimab in combination with SHR-8068 in patients with locally advanced or metastatic non-small cell lung cancer; Phase II: To explore the efficacy of SHR-A2102 in combination with adebelimab in combination with SHR-8068 in patients with locally advanced or metastatic non-small cell lung cancer.
This description comes directly from the study's public registry record.
Xin Xu · 0518-82342973 · xin.xu@hengrui.com
Yunfei Zhang · 0518-82342973 · yunfei.zhang.yz277@hengrui.com
There is no obligation to join — the study team can answer your questions about taking part.
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Inclusion Criteria: 1. Subjects are able to give voluntary informed consent, understand the study and are willing to follow and complete all the test procedures. 2. Age 18\~70 years old. 3. Pathologically confirmed unresectable locally advanced/metastatic non-small cell lung cancer. 4. At least one measurable lesion per RECIST v1.1 criteria. 5. ECOG PS score: 0-1. Exclusion Criteria: 1. Active or symptomatic brain metastases. 2. Previous diagnosis of any other malignancy. 3. Clinically symptomatic moderate to severe ascites; Uncontrollable or moderate or above pleural effusion, pericardial effusion. 4. Received anti-tumor therapy 4 weeks prior to initiation of study treatment. 5. Uncontrolled tumor-related pain. 6. Subjects with severe cardiovascular and cerebrovascular diseases.
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| Shanghai Chest Hospital | Shanghai, Shanghai Municipality, China | Recruiting |
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