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Tamoxifen and SUBA-Itraconzole Combination Testing in Ovarian Cancer (TICTOC)

NCT05156892 PHASE1 ACTIVE_NOT_RECRUITING

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.

Details

Lead sponsorAnthony Joshua, FRACP
PhasePHASE1
StatusACTIVE_NOT_RECRUITING
Enrolment44
Start dateSun Sep 04 2022 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionFri Jan 01 2027 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

Australia