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Investigation of 2X-121 in Patients With Advanced Ovarian Cancer Selected by the 2X-121 DRP® — PREDICT 2X-121  

Advanced Ovarian Cancer Clinical Trial

Official title:
Phase II, Prospective Open Label, Single Arm Study to Investigate Anti-tumor Effect and Tolerability of 2X-121 in Patients With Advanced Ovarian Cancer Selected by the 2X-121 DRP®

Clinical Trial Summary

This study is to be performed as an open label, multicenter, single arm study of 2X-121 to evaluate anti-tumor efficacy of 2X-121 as single agent therapy in a 28-days cycle in advanced ovarian cancer patients. 2X-121 will be supplied for oral administration twice daily as 600 mg (3 x 200 mg) capsules in a 28 days cycle. Patients with predicted high likelihood of responding to the drug (2X-121) using drug response prediction (DRP®), will be included in the study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03878849
Study type Interventional
Source Allarity Therapeutics
Contact
Status Active, not recruiting
Phase Phase 2
Start date April 15, 2019
Completion date March 2025
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