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Clinical Trial Summary

In phase Ia study, the safety and tolerability of SI-B001 in patients with locally advanced or metastatic epithelial malignancies will be investigated to determine the dose-limiting toxicity (DLT), maximum tolerated dose (MTD) of SI-B001. In the phase Ib study, the safety and tolerability of SI-B001 at the phase Ia recommended dose will be further investigated, and recommended phase II dose (RP2D) for phase II clinical studies will be determined. In addition, the preliminary efficacy, pharmacokinetic characteristics, and immunogenicity of SI-B001 in patients with locally advanced or metastatic epithelial tumors will be evaluated.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Locally Advanced or Metastatic Epithelial Tumor
  • Neoplasms, Glandular and Epithelial

NCT number NCT04603287
Study type Interventional
Source Sichuan Baili Pharmaceutical Co., Ltd.
Contact Hai Zhu
Phone +86-13980051002
Email zhuhai@baili-pharm.com
Status Recruiting
Phase Phase 1
Start date April 17, 2020
Completion date April 2024