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Clinical Trial Summary

In phase Ia study, the safety and tolerability of BL-B01D1 in patients with locally advanced or metastatic solid tumor will be investigated to determine the dose-limiting toxicity (DLT), maximum tolerated dose (MTD) of BL-B01D1. In phase Ib study, the safety and tolerability of BL-B01D1 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 BL-B01D1 in patients with locally advanced or metastatic solid tumor will be evaluated.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Locally Advanced or Metastatic Solid Tumor
  • Neoplasms

NCT number NCT05194982
Study type Interventional
Source Sichuan Baili Pharmaceutical Co., Ltd.
Contact Hai Zhu, PHD
Phone +86-13980051002
Email zhuhai@baili-pharm.com
Status Recruiting
Phase Phase 1
Start date November 29, 2021
Completion date August 2024

See also
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Completed NCT03601897 - A Phase 1b/2 Study of Rebastinib (DCC-2036) in Combination With Paclitaxel in Patients With Advanced or Metastatic Solid Tumors Phase 1/Phase 2
Completed NCT03717415 - A Study of Rebastinib (DCC-2036) in Combination With Carboplatin in Patients With Advanced or Metastatic Solid Tumors Phase 1/Phase 2
Recruiting NCT05461768 - A Study of BL-M07D1 in Patients With Locally Advanced or Metastatic HER2 Positive/Low Expression Breast Cancer and Other Solid Tumors Phase 1