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Clinical Trial Summary

Objective: To explore the efficacy, safety and tolerability of BL-B01D1, SI-B003 and BL-B01D1+SI-B003 in patients with recurrent or metastatic cervical cancer and other gynecological malignancies, and to further explore the optimal dose and mode of combination.


Clinical Trial Description

Objective: To explore the efficacy of BL-B01D1 monotherapy, SI-B003 monotherapy, and BL-B01D1+SI-B003 combination therapy in patients with recurrent or metastatic cervical cancer. To explore the safety and tolerability of BL-B01D1 monotherapy, SI-B003 monotherapy and BL-B01D1+SI-B003 combination therapy in patients with recurrent or metastatic cervical cancer and other gynecological malignancies, and to further explore the optimal dose and mode of combination therapy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05990803
Study type Interventional
Source Sichuan Baili Pharmaceutical Co., Ltd.
Contact Hai Zhu, PHD
Phone +8613980051002
Email zhuhai@baili-pharm.com
Status Recruiting
Phase Phase 2
Start date November 6, 2023
Completion date November 2025

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