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Clinical Trial Summary

To evaluate the safety and tolerability of SCB-313 in patients with peritoneal carcinomatosisa, to determine the maximum tolerated dose (MTD) and/or extended study recommended dose (RDE) for SCB-313 intraperitoneal injection, providing a basis for dosing regimen and dose choosing in clinical trial subsequently.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04047771
Study type Interventional
Source Sichuan Clover Biopharmaceuticals, Inc.
Contact
Status Terminated
Phase Phase 1
Start date September 10, 2019
Completion date May 5, 2022

See also
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