Cyclic Versus Daily Teriparatide on Bone Mass

Osteoporosis Clinical Trial

Official title:

Cyclic Versus Daily Teriparatide on Bone Mass

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00668941
• Other study ID #: R01 AR056651-01A2, 5RO1 ARO5
• Secondary ID: R01AR056651-01A2
• Status: Active, not recruiting
• Phase: Phase 2
• First received: April 27, 2008
• Last updated: August 9, 2017
• Start date: September 2005
• Est. completion date: November 2017

Study information

• Verified date: August 2017
• Source: Helen Hayes Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Osteoporosis is a disease that affects millions of individuals in the United States and abroad. It leads to decreased bone mass and causes an increased risk of fracture. This study will compare continuous versus cyclic treatment with teriparatide combined with alendronate, another drug for osteoporosis, or teriparatide alone in women with osteoporosis.

Description:

Osteoporosis is a serious bone disease that has become an important public health problem. It causes significant loss of bone mass and increases the risk of both fracture and architectural problems with the skeleton. Until recently, the treatments available for osteoporosis primarily prevented further deterioration of bone by reducing the rate of remodeling within the skeleton. This can reduce the risk of fracture by approximately 50%. Teriparatide is a new type of drug for people with osteoporosis who are at high risk of fracture. Teriparatide stimulates bone remodeling and can correct the underlying architectural and bone mass abnormalities that are characteristic of osteoporosis. This study will compare continuous versus cyclic treatment with teriparatide combined with alendronate, another drug for osteoporosis, or teriparatide alone in women with osteoporosis.

All participants have completed a parent study of two years that included a screening visit with a physical exam, blood draw, x-rays, EKG, and distribution of calcium and vitamin D supplements. Participants will be separated into two groups according to the treatment they have undergone over the year prior to study entry. Participants who have taken alendronate for at least 1 year prior to study entry will be assigned to Protocol 1. Participants who have not previously taken alendronate will be assigned to Protocol 2. Participants in both protocols will be randomly assigned to one of the following three biopsy groups: pre-treatment; early; or late. Participants in the pre-treatment biopsy group will have a bone biopsy before treatment begins. Those participants in the early biopsy group will have a biopsy at Week 7 of treatment, and those in the late group will have a biopsy at Month 7.5 of treatment.

Participants will also be randomly assigned to one of three treatment schedules. Participants in Protocol 1 may be assigned to receive alendronate alone for 24 months; teriparatide daily plus alendronate for 24 months; or teriparatide daily on and off for 3 months at a time plus alendronate for 24 months. Participants in Protocol 2 may be assigned to receive only the supplements they were given during the screening visit; teriparatide daily plus alendronate for 24 months; or teriparatide daily on and off for 3 months at a time for 24 months. Participants will attend assessment visits at Weeks 4 and 7 and Months 3, 5, 6, 7.5, 9, 12, 15, 18, 21, and 24. Visits may include bone turnover measurements, bone mass scans, walking tests, questionnaires, CT scans, and blood draws.

A recently funded extension study will extend the treatment period from 24 to 48 months for all consenting. If the individual was assigned to teriparatide daily (with or without alendronate), they will be given alendronate for the 24 to 48 month time period. If the individual was assigned to cyclic teriparatide, they will continue cyclic therapy foro the 24-48 month period (with or without alendronate).

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 140
• Est. completion date: November 2017
• Est. primary completion date: February 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 45 Years to 85 Years

Eligibility

Inclusion Criteria:

• Diagnosis of osteoporosis or T score below -2 plus one or more osteoporosis related fractures

• Two measurable vertebrae between L1 and L4

• Willing to undergo a single iliac crest biopsy after administration of 4 tetracycline labels

Exclusion Criteria:

• Secondary causes of osteoporosis or presence of a skeletal disorder other than osteoporosis

• Uses drugs likely to affect skeletal or calcium homeostasis

• Multiple vertebral fractures or severe degenerative changes with fewer than two evaluable vertebrae

• Unwilling to undergo a single iliac crest biopsy

• History of allergy to tetracyclines, exposure to tetracyclines within the last year, or any remote long term use of tetracyclines

• Current use of anti-resorptive medicines (other than alendronate for half the female participants)

• Use of hormone therapy, estrogen therapy, raloxifene, or calcitonin within 6 months before study entry

• Use of any bisphosphonate for more than 3 months within 2 years before study entry (only applies to participants in Groups 4, 5, and 6)

• History of a kidney stone within 5 years before study entry or any history of multiple kidney stones

• Hypercalcemia, hypercalciuria, or elevated parathyroid hormone (reduced 25-hydroxyvitamin D will be corrected prior to admission)

• Esophageal ulceration or stricture or known hypersensitivity to bisphosphonates

• History of external radiation therapy

• Unlikely or unable to complete the study, as determined by the investigators

• Illicit drug use or excessive alcohol consumption

Related Conditions & MeSH terms

• Osteoporosis

Intervention

Drug:
• Teriparatide
Teriparatide will be given subcutaneously in 20-mcg doses either continuously or cyclically.
• Alendronate
Participants will take 70 mg per week of alendronate for 48 months.

Dietary Supplement:
• Calcium
Calcium supplements will be administered in varied amounts for all participants, but each participant will take enough to bring her total daily calcium intake to 1,200 mg.
• Vitamin D3
Vitamin D3 supplements will be administered in varied amounts for all participants, but each participant will take enough to bring her total daily intake to 1,200 mg.

Locations

Country	Name	City	State
United States	Helen Hayes Hospital	West Haverstraw	New York

Sponsors (3)

Lead Sponsor	Collaborator
Helen Hayes Hospital	Health Research, Inc., National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Bone density		24 and 48 months
Secondary	Histomorphometry of iliac crest bone biopsies		Measured at Week 7 and Month 7
Secondary	HRpQCT (tibia, radius) and QCT (spine and hip)and FEA of these QCT scans		48 months