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Clinical Trial Summary

The study's purpose is to understand the effects of a new treatment (suba-itraconazole and tamoxifen) in epithelial ovarian cancer. Who is it for? Patients may be eligible to join this study with ovarian cancer resistant to platinum-based chemotherapy agents Study Details: Participants will receive different doses of tamoxifen and suba-itraconazole to determine the optimal combination dose. Participants will be seen by the investigators once a week for the first 3 weeks and then once every 4 weeks. Participant will be reviewed by a clinician and undergo regular blood tests, cardiac monitoring and imaging assessments.


Clinical Trial Description

A phase 1/2 study of Suba-itraconazole and Tamoxifen in platinum resistant ovarian carcinoma ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05156892
Study type Interventional
Source St Vincent's Hospital, Sydney
Contact Anthony Joshua, FRACP, MBBS, PhD
Phone +61 293555655
Email Anthony.Joshua@svha.org.au
Status Recruiting
Phase Phase 1
Start date September 4, 2022
Completion date January 1, 2025

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