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Completed Phase 3 Interventional Results available

A Study to Test if TVB-009P is Effective in Relieving Postmenopausal Osteoporosis

ClinicalTrials.gov ID: NCT04729621

Public ClinicalTrials.gov record NCT04729621. 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 Oct 23, 2026, 8:39 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

A Randomized, Double-Blind, Multinational, Multicenter Study to Compare Efficacy, Safety, and Immunogenicity of TVB-009P and Denosumab (Prolia®) in Patients With Postmenopausal Osteoporosis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to demonstrate similar efficacy and safety between TVB-009 and Prolia® (denosumab)

Study identification

NCT ID
NCT04729621
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Teva Pharmaceuticals USA
Industry
Enrollment
332 participants

Conditions and interventions

Interventions

Combination Product

Eligibility (public fields only)

Age range
60 Years to 90 Years
Sex
Female
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
Mar 22, 2021 (Actual)
Primary completion
Dec 31, 2022 (Actual)
Completion
Jun 19, 2023 (Actual)
Last update posted
Oct 1, 2026

2021 – 2023

United States locations

U.S. sites
20
U.S. states
8
U.S. cities
20
Facility City State ZIP Site status
Teva Site 103 Phoenix Arizona 85004 —
Teva Site 119 Tucson Arizona 85704 —
Teva Site 118 San Diego California 92111 —
Teva Site 107 New London Connecticut 06320 —
Teva Site 115 Coral Gables Florida 33134 —
Teva Site 114 Edgewater Florida 32132 —
Teva Site 116 Lake City Florida 32055 —
Teva Site 109 Miami Lakes Florida 33014 —
Teva Site 117 Miami Springs Florida 33166 —
Teva Site 110 Oldsmar Florida 34677 —
Teva Site 120 Orlando Florida 32801 —
Teva Site 102 Ormond Beach Florida 32174 —
Teva Site 101 Port Saint Lucie Florida 34952 —
Teva Site 111 Sarasota Florida 34239 —
Teva Site 104 Tamarac Florida 33321 —
Teva Site 112 Henderson Nevada 89014 —
Teva Site 113 North Las Vegas Nevada 89030 —
Teva Site 105 Albuquerque New Mexico 87106 —
Teva Site 108 Duncansville Pennsylvania 16635 —
Teva Site 106 Seattle Washington 98105 —

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 58 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04729621, 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 Oct 1, 2026 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04729621 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →