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Clinical Trial Summary

The goal of this study is to find the highest tolerated dose of NC-6300 that can be given to patients with advanced solid tumors or soft tissue sarcoma. The safety and tolerability of the drug will also be studied.


Clinical Trial Description

The first part of the study will determine the maximum tolerated dose (MTD), dose-limiting toxicities (DLTs), and the recommended Phase 2 (RPII) dose of NC-6300. The second part of the study will assess the activity and tolerability of NC-6300 in patients with soft tissue sarcoma. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03168061
Study type Interventional
Source NanoCarrier Co., Ltd.
Contact Amanda Knight
Phone +1 919 443 3476
Email aknight@cato.com
Status Recruiting
Phase Phase 1/Phase 2
Start date June 30, 2017
Completion date July 2020

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