Clinical Trials Directory

Trials / Terminated

TerminatedNCT01857817

Efficacy and Safety Study of Etodolac and Propranolol in Patients With Clinically Progressive Prostate Cancer

A Randomized, Placebo Controlled, Multicenter Phase 2 Study of Etodolac and Propranolol in Patients With Clinically Progressive Prostate Cancer

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
35 (actual)
Sponsor
Vicus Therapeutics · Industry
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the clinical benefit of the co-administration of propranolol and etodolac (VT-122 therapy) in patients with clinically progressive prostate cancer.

Conditions

Interventions

TypeNameDescription
DRUGVT-122The following will be used in the study for VT-122: propranolol 22 mg immediate-release capsules and etodolac 340 mg capsules.
DRUGPlaceboThe placebo capsules will be prepared to match the active drug.

Timeline

Start date
2013-06-01
Primary completion
2016-04-01
Completion
2016-04-01
First posted
2013-05-20
Last updated
2018-04-26

Locations

16 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01857817. Inclusion in this directory is not an endorsement.

Efficacy and Safety Study of Etodolac and Propranolol in Patients With Clinically Progressive Prostate Cancer (NCT01857817) · Clinical Trials Directory