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Completed Phase 2 Interventional

Safety and Efficacy of Multiple Dosing Regimens of BPS804 in Post Menopausal Women With Low Bone Mineral Density

ClinicalTrials.gov ID: NCT01406548

Public ClinicalTrials.gov record NCT01406548. 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 Jul 23, 2026, 1:17 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

A Randomized, Double-blind, Placebo-controlled, Multiple Dose Study to Assess the Safety and Efficacy of Multiple Dosing Regimens of BPS804 in Post Menopausal Women With Low Bone Mineral Density

Study identification

NCT ID
NCT01406548
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ultragenyx Pharmaceutical Inc
Industry
Enrollment
44 participants

Conditions and interventions

Interventions

  • BPS804 20mg/Kg Drug
  • Placebo to 20mg/Kg BPS804 Drug

Drug

Eligibility (public fields only)

Age range
45 Years to 85 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
Jun 30, 2011
Primary completion
Sep 30, 2013
Completion
Sep 30, 2013
Last update posted
Sep 14, 2022

2011 – 2013

United States locations

U.S. sites
5
U.S. states
4
U.S. cities
4
Facility City State ZIP Site status
Novartis Investigative Site Anaheim California 92801-2811
Novartis Investigative Site Miami Florida 33126
Novartis Investigative Site Miami Florida 33175
Novartis Investigative Site Berlin New Jersey 08009
Novartis Investigative Site Duncansville Pennsylvania 16635

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01406548, 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 Sep 14, 2022 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01406548 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →