ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

TAVT-45 (Abiraterone Acetate) Granules in Patients With Prostate Cancer

ClinicalTrials.gov ID: NCT04887506

Public ClinicalTrials.gov record NCT04887506. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Apr 29, 2026, 12:17 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 3 Study Investigating the Efficacy and Safety of TAVT-45 (Abiraterone Acetate) Granules for Oral Suspension (Novel Abiraterone Acetate Formulation) Relative to a Reference Abiraterone Acetate Formulation in Patients With mCSPC & mCRPC

Study identification

NCT ID
NCT04887506
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Tavanta Therapeutics
Industry
Enrollment
107 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 4, 2021
Primary completion
Oct 19, 2022
Completion
Oct 19, 2022
Last update posted
Jan 15, 2024

2021 – 2022

United States locations

U.S. sites
13
U.S. states
12
U.S. cities
13
Facility City State ZIP Site status
Research Site Homewood Alabama 35209
Research Site Tucson Arizona 85715
Research Site Little Rock Arkansas 72211
Research Site Los Angeles California 90048
Research Site San Bernardino California 92404
Research Site Denver Colorado 80211
Research Site Bradenton Florida 34205
Research Site Meridian Idaho 83642
Research Site Jeffersonville Indiana 47130
Research Site Annapolis Maryland 21401
Research Site Troy Michigan 48084
Research Site New York New York 10016
Research Site Virginia Beach Virginia 23462

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 29 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04887506, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 15, 2024 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04887506 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →