Condition: Solid Tumor · Sponsor: The First Affiliated Hospital with Nanjing Medical University
This study is a single-center exploratory clinical trial. It is estimated that 9-24 subjects will be enrolled. The "3+3" dose escalation design is adopted. The main purpose is to evaluate the safety of RD133 in the treatment of subjects with relapsed or refractory MSLN-positive solid tumors and explore the Recommend phase II dose of RD133 in the treatment of patients with relapsed/refractory MSLN-positive solid tumors.
This description comes directly from the study's public registry record.
Lingxiang Liu · llxlau@163.com
Always discuss trial participation with your own doctor first.
| The First Affiliated Hospital with Nanjing Medical University | Nanjing, Jiangsu, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05166070