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Clinical Trial Summary

The purpose of this study is to assess the safety, tolerability, and efficacy of CBX-12 in female subjects with platinum resistant or refractory ovarian cancer at 2 doses; 125 mg/m2 every 21 days or 100 mg/m2 every 21 days.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06315491
Study type Interventional
Source Cybrexa Therapeutics
Contact Clinical Operations Trial Team
Phone 860-717-2731
Email clinicalstudies@cybrexa.com
Status Not yet recruiting
Phase Phase 2
Start date July 2024
Completion date April 2026

See also
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