Current partner codePEPTIDESDE
NCT00131469·Phase 4·INTERVENTIONAL

Study of Teriparatide (FORTEO) to Treat Adults With Osteogenesis Imperfecta

Status

Completed

Phase

Phase 4

Enrollment

79

Locations

3

Results

Posted

Publications

1

Study summary

What the protocol is testing.

The purpose of this study is to determine the effectiveness of teriparatide (FORTEO), which is human parathyroid hormone 1-34, for increasing bone mass and improving bone structure in adults affected with Osteogenesis Imperfecta (OI).

Full detailed description

The purpose of this study is to determine the effectiveness of teriparatide (FORTEO), which is human parathyroid hormone 1-34, for increasing bone mass and improving bone structure in adults affected with Osteogenesis Imperfecta (OI). Osteogenesis imperfecta is an inherited disorder of type I collagen, a major component of bones, and is characterized by multiple fractures and deformities. OI affects approximately 1-2 of every 10,000 individuals. Virtually all of the studies of potential treatments for OI have evaluated the effects of medications only on children with OI. There is no cure for osteogenesis imperfecta and there is no established medical therapy for adults with the disorder. There are very limited data concerning the usefulness of parathyroid hormone therapy in OI. An effective anabolic therapy for the treatment of adult patients with OI could be a valuable asset to the affected patients. In this study, the working hypothesis is that individuals affected with OI who are treated with Forteo will experience increased spine and hip bone mineral density and an increase in bone strength. Although Forteo is not expected to change the defect in the collagen produced, but is postulated to increase the quantity of bone formed and improve bone strength. This will be a placebo controlled, double blinded trial; half the patients will receive Forteo 20 ug/day SQ. Adult patients (age at least 18 yrs) with OI will be enrolled for a treatment duration of 18 months. Blood, urine, and bone density/strength tests will be done during the study to assess efficacy and safety.

Interventions

Treatment arms and agents.

DRUG

Teriparatide (FORTEO)

Teriparatide (FORTEO) 20mcg, subcutaneous injection, once daily

DRUG

Placebos

Timeline

From registration to results.

  1. First posted

    Aug 18, 2005

  2. Study start

    Jun 2005

  3. Primary completion

    Jan 2011

  4. Study completion

    Jan 2011

  5. Results posted

    Apr 24, 2019

  6. Registry updated

    Apr 24, 2019

Outcomes

What the study measures.

Primary outcomes

Spine Bone Mineral Density (BMD)

Time frame · baseline and 18 months

bone density by dual energy xray absorptiometry

Secondary outcomes

Total Hip BMD

Time frame · baseline and 18 months

bone density by dual energy xray absorptiometry

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
85 Years
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * Previous established diagnosis of Osteogenesis Imperfecta AND * \> 2 previous adult fractures, AND/OR * BMD at lumbar spine, femoral neck or total hip T score \< -2.0 Exclusion Criteria: * Open epiphyses. * History of external beam radiation to the skeleton. * Pagets disease. * Bone metastases or skeletal malignancies. * Total lifetime exposure to any antiresorptive medication \< 90 days (Primary Inclusion). * Treatment with any antiresorptive medication 12 months proceeding enrollment - (Secondary Inclusion). * Women with OI who are pregnant or unwilling to use 1 form of contraception. * Vitamin D insufficiency (25-hydroxyvitamin D \<15ng/ml)

Study locations

3 registered sites.

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

Kennedy Krieger Institute

Baltimore, Maryland, United States

Oregon Health & Science University

Portland, Oregon, United States

Baylor College of Medicine, Department of Molecular and Human Gentics

Houston, Texas, United States

Related trials

More studies on Teriparatide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.