Viewing Study NCT05156892


Ignite Creation Date: 2025-12-24 @ 3:07 PM
Ignite Modification Date: 2025-12-28 @ 11:18 AM
Study NCT ID: NCT05156892
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2025-05-15
First Post: 2021-10-19
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Tamoxifen and SUBA-Itraconzole Combination Testing in Ovarian Cancer
Sponsor: Anthony Joshua, FRACP
Organization:

Study Overview

Official Title: A Phase I/II Trial Investigating the Tolerability, Toxicity and Efficacy of Tamoxifen and SUBA-Itraconazole in Patients With Platinum Resistant Recurrent Epithelial Ovarian Cancer
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2025-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: TICTOC
Brief 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.
Detailed Description: A phase 1/2 study of Suba-itraconazole and Tamoxifen in platinum resistant ovarian carcinoma

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: