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Completed Phase 3 Interventional Results available

Comparative Efficacy and Safety Study of RGB-14-P and Prolia® in Women With Postmenopausal Osteoporosis

ClinicalTrials.gov ID: NCT05087030

Public ClinicalTrials.gov record NCT05087030. 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 May 17, 2026, 5:14 AM 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 Randomised, Double Blind, Multicentre Phase III Study to Assess the Efficacy and Safety of RGB-14-P Compared to Prolia® in Women With Postmenopausal Osteoporosis

Study identification

NCT ID
NCT05087030
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Gedeon Richter Plc.
Industry
Enrollment
473 participants

Conditions and interventions

Interventions

  • Prolia® Drug
  • RGB-14-P Drug

Drug

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
Sep 20, 2021
Primary completion
Oct 1, 2023
Completion
Nov 14, 2023
Last update posted
Oct 23, 2024

2021 – 2023

United States locations

U.S. sites
4
U.S. states
3
U.S. cities
4
Facility City State ZIP Site status
Miami Clinical Research Miami Florida 33155
Global Health Research Center Miami Lakes Florida 33016
iResearch Atlanta, LLC Decatur Georgia 30030
Excel Clinical Research - Internal Medicine Las Vegas Nevada 89109

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 55 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05087030, 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 23, 2024 · Synced May 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05087030 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →