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Trial · Interventional

CompletedPhase 2Results postedRegistry data

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

This trial does not test a peptide that PepBank tracks.

  • Names Calcitonin-salmon, does not test it. It appears in the title.

Overview

Status
Completed
Phase
Phase 2
Enrollment
129 participants (actual)
Sponsor
Tarsa Therapeutics, Inc. · Industry
Design
Randomized · Triple masking
Countries
1 country

United States

Start
Jan 2011
Primary completion
May 2012
Completion
Jul 2012
First posted
9 Feb 2011 (estimated)
Last update posted
12 Sept 2014 (estimated)
Conditions
Osteopenia

Timeline

1 trial · 1 completed · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
201120122013
  1. Ph 2

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

    NCT01292187

    Jan 2011 to Jul 2012

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

The primary purpose of this study was to evaluate the efficacy of oral calcitonin (rsCT)tablets in the prevention of bone loss in postmenopausal women with lower bone mineral density at increased risk of fracture. The secondary purpose of this study was to determine if there is any food effect by comparing the efficacy and safety of oral calcitonin tablets administered at dinner or at bedtime.

Interventions

  • Oral calcitonin at dinnertimeDrug
  • Oral placebo at dinnertimeDrug
  • Oral calcitonin at bedtimeDrug
  • Oral placebo at bedtimeDrug

Arms2

  • Experimental

    Oral calcitonin at dinner-or bedtime

    Intervention: Oral calcitonin at dinnertime or oral calcitonin at bedtime. Postmenopausal subjects with osteopenia were treated for one year (also with vitamin D and calcium supplements) to determine if oral calcitonin tablets would prevent the loss of bone mineral density compared with placebo. Randomization to active or placebo was done 2:1. After randomization, further randomization was done to divide each arm into two groups, one in which dosing was at dinnertime and the other in which dosing was at bedtime to determine if food affected efficacy or safety.

  • Experimental

    Oral placebo at dinner- or bedtime

    Intervention: oral placebo at dinnertime or oral placebo at bedtime

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Percentage Change From Baseline to Week 54 of Lumbar Spine Bone Mineral Density of Active Compared to Placebo.

    Time frame · Baseline, Week 54

Secondary outcomes(1)
  1. Percentage Change From Baseline to Week 54 of Plasma CTx-1 Following rsCT Compared to Placebo.

    Time frame · Baseline, Week 54

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

Primary outcome results

Primary outcomeLeast squares mean· Baseline, Week 54

Percentage Change From Baseline to Week 54 of Lumbar Spine Bone Mineral Density of Active Compared to Placebo.

GroupValue (percent change)
Oral Calcitonin Tablets1.03
Oral Placebo Tablets-0.12
Secondary and other outcome results(1)
Secondary outcomeLeast squares mean· Baseline, Week 54

Percentage Change From Baseline to Week 54 of Plasma CTx-1 Following rsCT Compared to Placebo.

GroupValue (percent change)
Oral rsCT Tablets-11.83
Oral Placebo Tablets8.37

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther events
Oral rsCT TabletsTablets containing 200 μg of recombinant salmon calcitonin, for oral administration. At group assignment the first 60 patients were told to self-administer the tablets once daily at bedtime (Group 1). The remaining patients were told to self-administer once daily at dinner time (Group 2)to determine if there was any food effect. Randomization was done active:placebo, 2:1.–6 / 8633 / 86
Oral Placebo TabletsIdentical appearing placebo tablets, without active ingredient At group assignment the first 60 patients were told to self-administer the tablets once daily at bedtime Group 1). The remaining patients enrolled were told to self-administer once daily at dinner time (Group 2)to determine if there was any food effect. Randomization was done active:placebo, 2:1.–2 / 4315 / 43

Each cell reads participants affected / participants at risk, as the registry posted them.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies0

Studies that cite this trial.

No study cites this trial.

Eligibility

Who could join, as posted.

Sex
Female
Age
from 45 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Female and at least 45 years of age. * Must have undergone the onset of spontaneous or surgical menopause more than 5 years prior to entry. Spontaneous menopause is defined as 12 months of spontaneous amenorrhea. Surgical menopause is defined as ≥ 6 weeks postsurgical bilateral oophorectomy with or without hysterectomy. * Serum follicle-stimulating hormone (FSH) levels must be ≥ 30 mIU/mL. * A body mass index (BMI) of not greater than 35 (BMI =weight \[kg\]/height\[m\]2). * Bone mineral density (BMD) T-score between -1.0 and - 2.5 at the total hip, femoral neck, trochanter, or lumbar spine. * Additional risk factors such that the 10 year risk of a major osteoporotic fracture or hip fracture risk is at least as great as a 65-year-old woman of the same race and BMI of 25 kg/m2 as determined by the FRAX algorithm . * No clinically significant abnormal findings in the medical history or physical exam that would preclude participation in the investigator's opinion. * No clinically significant abnormal laboratory values at the screening assessment. * Subjects must give written informed consent after reading the Subject Information and Consent Form and having had the opportunity to discuss the study with the investigator. Exclusion Criteria: * History of an osteoporotic fracture, defined as a fracture at the wrist, hip, or humerus occurring from a fall at standing height or less. * BMD T-Score at any site ≤ -2.5. * Current treatment (or within 3 months prior to randomization) with hormone replacement therapy. * History of metabolic and other bone diseases, including osteogenesis imperfecta, osteomalacia, and Paget's disease. * Vitamin D insufficiency defined as a 25 hydroxyvitamin D level \< 20 ng/mL (50 nmol/L). * Prior use of calcitonin, ever. * Prior use of any bisphosphonate, ever. * Prior use of denosumab, fluoride, or strontium, ever. * Prior use of parathyroid hormone analogs, ever. * Any condition or disease that may interfere with the ability to have a dual energy x-ray absorptiometry (DXA) scan or to evaluate a DXA scan, for example, severe osteoarthritis of the spine, spinal fusion, pedicle screws, history of vertebroplasty, or degenerative disease that results in insufficient number of evaluable lumbar vertebrae, bilateral hip replacements. * Use of anabolic steroids or androgens within 6 months preceding randomization. * Use of vitamin D metabolites and analogs, (e.g., calcitriol) within 3 months preceding randomization). Note: Vitamin D supplementation is not exclusionary. * Use of estrogen or estrogen-related drugs (including selective estrogen receptor molecules), for example, tamoxifen, tibolone, or raloxifene within 3 months preceding randomization. * Chronic systemic treatment with glucocorticoids. * Clinically relevant abnormal history, physical findings, or laboratory values at the pre-study screening assessment that could interfere with the objectives of the study or the safety of the subject. * Presence of acute or chronic illness or history of chronic illness which, in the judgment of the investigator, makes participation in the study medically inappropriate. * Known acquired immune deficiency syndrome (AIDS) or human immunodeficiency virus (HIV) seropositivity. * Uncontrolled hypertension, significant gastrointestinal abnormalities, uncontrolled diabetes mellitus, significant coronary heart disease, any psychotic mental illness, chronic allergic rhinitis, asthma, uncorrected endocrine dysfunction, or significantly impaired hepatic, respiratory, or renal function. * Participation in any other clinical study within the previous month. * History of drug or alcohol abuse, or intake of more than 30 units of alcohol weekly. * Possibility that the subject will not cooperate with the requirements of the protocol. * Known sensitivity to sCT. * Shift workers-individuals who are at work during overnight hours.

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