Current partner codePEPTIDESDE
NCT01656629·Not applicable·INTERVENTIONAL

Stem Cell Recruitment in Osteoporosis Therapy

Status

Terminated

Phase

Not applicable

Enrollment

55

Locations

1

Results

Posted

Publications

0

Study summary

What the protocol is testing.

Osteoporosis is an important health problem in the rapidly-aging demographic. Fragility fractures are devastating consequences of osteoporosis. The most common treatment approach in osteoporosis is inhibition of bone resorption with drugs like alendronate (ALN). Parathyroid hormone (PTH) stimulates bone formation and is the only anabolic drug available. Dual therapy with ALN and PTH is not as effective as single-drug therapy in preventing fracture. Bone progenitor cells (MSCs) are recruited to sites of bone remodeling when a growth factor called Transforming Growth Factor Beta (TGF-β1) is released from bone. Different osteoporosis medicines may have differing effects on this process. The effects of ALN versus PTH on bone progenitor recruitment in humans are unknown. This is a randomized, clinical trial of ALN, PTH, and calcium and vitamin D in post-menopausal women with low bone mass. Women will be treated for 3 months with ALN or PTH or calcium and vitamin D. Data collected will include bone biopsies for histomorphometry and micro computed tomography (µCT), bone marrow aspirates for molecular studies, peripheral blood to detect circulating bone progenitor cells and dual X-ray absorptiometry. The investigators hypothesize that in humans, PTH will 1) increase bone progenitor number, 2) enhance recruitment of bone progenitor cells to bone resorption sites, and 3) increase bone progenitor number in peripheral circulation. Furthermore, the investigators hypothesize that ALN treatment will have the opposite effect. Understanding the differences in bone progenitor cell activity and recruitment during osteoporosis therapy will provide a mechanistic rationale for effective use of PTH and anti-resorptive drugs in osteoporosis treatment.

Interventions

Treatment arms and agents.

DRUG

Teriparatide

20 mcg subq daily for 3 months

DRUG

Alendronate

70 mg weekly for 3 months

DIETARY_SUPPLEMENT

calcium and vitamin D

Timeline

From registration to results.

  1. First posted

    Aug 3, 2012

  2. Study start

    Aug 2012

  3. Primary completion

    Jun 2014

  4. Study completion

    Aug 7, 2020

  5. Results posted

    Aug 8, 2019

  6. Registry updated

    Aug 21, 2020

Outcomes

What the study measures.

Primary outcomes

The Percent Change in Circulating Osteoprogenitor Cells as Assessed by Flow Cytometry in the Blood Before and After Treatment With Parathyroid Hormone (PTH) or Alendronate (ALN).

Time frame · up to 3 months

Secondary outcomes

Difference in Bone Formation as Assessed by Bone Histomorphometry on Bone Biopsy Between Treatment Groups

Time frame · 3 months

Difference in Osteogenic Potential of Bone Marrow as Measure by Colony Forming Unit Osteoblast (CFU-Ob) Assays Between Treatment Groups

Time frame · 3 months

Eligibility

Who can take part.

Minimum age
50 Years
Maximum age
80 Years
Sex
FEMALE
Healthy volunteers
No

Inclusion Criteria: * Post-menopausal women aged 50-80 years * T score \< -2.5 at lumbar spine, total hip or femoral neck on dual x-ray absorptiometry (DXA) OR T score \< -1.5 with a personal or family history of fracture Exclusion Criteria: * Previous use of bisphosphonates or Teriparatide; current estrogen therapy; any other osteoporosis therapy in the past 6 months * Metabolic bone disease other than osteoporosis * Body mass index (BMI) \< 18 * Weight \> 325 lbs * Current smoking or current alcohol use that exceeds 3 units of alcohol daily * Use of medications known to affect bone metabolism * Renal disease, history of kidney stones or hypercalciuria * Hypo- or hyperparathyroidism; hypo- or hypercalcemia * Serum vitamin D level \< 20 ng/dL * Refusal to adjust their dietary calcium to \<750mg (i.e. two servings per day of calcium rich food) * History of bone marrow or organ transplant * History of malignancy or radiation to the bone * History of esophageal stricture, dysmotility or severe reflux disease * Gastrointestinal malabsorption * Use of digoxin * Need for chronic anticoagulation therapy such as Coumadin, heparin or low molecular weight heparin or inability to discontinue anti-platelet medication * Bleeding diathesis; hemoglobin ≤ 12.5 g/dL (American Red Cross cut-off to donate blood) * International normalized ratio (INR) pro time \> 1.1 or activated partial thromboplastin time (APT) T ratio \> 1.2 * Platelets \< 150K/cu mm * Cellulitis at site of iliac crest * History of allergy to medications used in bone biopsy (demeclocycline, lidocaine) * Inability to understand and provide informed consent.

Study locations

1 registered sites.

United States. Showing up to 24 locations stored in the fast local snapshot.

Johns Hopkins Bayview Medical Center

Baltimore, Maryland, United States

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Teriparatide.

Related PeptideStat pages

Put the record in context.

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