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NCT04457089 · ClinicalTrials.gov registry record · Early Phase 1

Statin Therapy to Reduce Progression in Women With Platinum Sensitive Ovarian Cancer

A Early Phase 1 study of Recurrent Ovarian Cancer and Platinum-sensitive Ovarian Cancer, sponsored by Marc Goodman.

Completed
Registry status
Early Phase 1
Development phase
18
Enrollment target
1
Study location

NCT04457089: Completed Early Phase 1 study of Recurrent Ovarian Cancer and Platinum-sensitive Ovarian Cancer, sponsored by Marc Goodman.

NCT04457089 is a Early Phase 1 study of Recurrent Ovarian Cancer and Platinum-sensitive Ovarian Cancer that has completed, run by Marc Goodman. The registered enrollment target is 18 participants, below the 188-participant average among 6 other Recurrent Ovarian Cancer trials with a reported enrollment target (90% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04457089, a Early Phase 1 study of Recurrent Ovarian Cancer and Platinum-sensitive Ovarian Cancer, has completed, sponsored by Marc Goodman.

COMPLETED
Registry status
Early Phase 1
Development phase
18 participants
Enrollment target
1
Study location

Study Summary

This is a single arm pilot trial to evaluate the feasibility of using a simvastatin intervention, and to evaluate its effects on cancer progression, among 20 patients with platinum-sensitive ovarian cancer, treated with carboplatin and liposomal doxorubicin at Cedars-Sinai Medical Center.

Primary Outcome

Percentage of patients who complete the simvastatin intervention with at least 85% compliance during Carboplatin and Doxil chemotherapy.

Interventions

  • DRUG Simvastatin 40mg

Study Locations (1)

California

  • Cedars Sinai Medical Center - Los Angeles

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2021-01-25
Est. Completion 2025-05-12
Phase Early Phase 1
Marc Goodman

2 total trials

What the finished NCT04457089 record still lists

NCT04457089 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 188-participant average among 6 other Recurrent Ovarian Cancer trials with a reported enrollment target (90% lower).

The record links to 2 conditions, with Recurrent Ovarian Cancer appearing as the primary indexed condition, and to 1 intervention - of which Simvastatin 40mg is the first listed.

NCT04457089 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT04457089 about?

NCT04457089 is a clinical study titled "Statin Therapy to Reduce Progression in Women With Platinum Sensitive Ovarian Cancer". This is a single arm pilot trial to evaluate the feasibility of using a simvastatin intervention, and to evaluate its effects on cancer progression, among 20 patients with platinum-sensitive ovarian cancer, treated with carboplatin and liposomal doxorubicin at Cedars-Sinai Medical Center.

What is the current status of trial NCT04457089?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 18 participants. The study started on 2021-01-25. Estimated completion is 2025-05-12.

What conditions does trial NCT04457089 study?

This clinical trial studies the following conditions: Recurrent Ovarian Cancer, Platinum-sensitive Ovarian Cancer.

What interventions are being tested in trial NCT04457089?

The interventions under investigation include: Simvastatin 40mg (DRUG).

Who is sponsoring clinical trial NCT04457089?

This trial is sponsored by Marc Goodman, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04457089 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT04457089, the US trial registry maintained by the National Library of Medicine. NCT04457089 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.