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Completed Phase 2 Interventional Results available

A Study of Oral Recombinant Salmon Calcitonin (rsCT) to Prevent Postmenopausal Osteoporosis

ClinicalTrials.gov ID: NCT01292187

Public ClinicalTrials.gov record NCT01292187. 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 22, 2026, 4:32 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 Randomized, Double-blind, Placebo-controlled Clinical Trial Evaluating the Safety and Efficacy of Oral Recombinant Salmon Calcitonin (rsCT) in the Prevention of Postmenopausal Osteoporosis in Women at Increased Risk of Fracture

Study identification

NCT ID
NCT01292187
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Tarsa Therapeutics, Inc.
Industry
Enrollment
129 participants

Conditions and interventions

Conditions

Interventions

  • Oral calcitonin at dinnertime Drug
  • Oral placebo at dinnertime Drug
  • Oral calcitonin at bedtime Drug
  • Oral placebo at bedtime Drug

Drug

Eligibility (public fields only)

Age range
45 Years and older
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
Dec 31, 2010
Primary completion
Apr 30, 2012
Completion
Jun 30, 2012
Last update posted
Sep 11, 2014

2011 – 2012

United States locations

U.S. sites
10
U.S. states
10
U.S. cities
10
Facility City State ZIP Site status
Diablo Clinical Research, Inc. Walnut Creek California 94598
Innovative Research of West Florida, Inc. Clearwater Florida 33756
Bethesda Health Research Bethesda Maryland 20817
Clinical Pharmacology Study Group Worcester Massachusetts 01610
Michigan Bone and Mineral Clinic Detroit Michigan 48236
The Osteoporosis Center at St. Luke's Hospital Chesterfield Missouri 63107
Comprehensive Clinical Research Berlin New Jersey 08009
University of Pittsburgh - Department of Neurology Pittsburgh Pennsylvania 15213
Puget Sound Osteoporosis Center Seattle Washington 98144
University of Wisconsin Hospital and Clinics Madison Wisconsin 53705

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 NCT01292187, 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 11, 2014 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01292187 live on ClinicalTrials.gov.

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