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Combined Administration of Teripapartide and Antiresorptive Agents in Postmenopausal Osteoporosis

Information source: Medical University of Vienna
ClinicalTrials.gov processed this data on August 20, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Osteoporosis

Intervention: teriparatide (Drug); teriparatide and raloxifene (Drug); teriparatide and alendronate (Drug)

Phase: Phase 4

Status: Completed

Sponsored by: Medical University of Vienna

Official(s) and/or principal investigator(s):
Christian Muschitz, M.D., Principal Investigator, Affiliation: Medical University of Vienna


Increased bone formation in the absence of accelerated resorption is resulting in a marked anabolic response to teriparatide (TPTD) during the early phase after treatment initiation. Months later, due to coupling mechanism, the sustained increase of bone formation and ongoing anabolic effects are accompanied by significantly increased bone resorption as well. Antiresorptives influence the balance of bone formation and resorption. Therefore the investigators aim is to investigate the effects of the addition of antiresorptives to the second half of TPTD cycle when resorption is already also markedly elevated.

Clinical Details

Official title: Phase IV Study Teriparatide and Antiresorptive Combination Treatment Subsequent to 9 Months of Teriparatide Monotherapy

Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome: Differences in changes of areal lumbar spine BMD between the three treatment groups

Secondary outcome: Differences in changes of BMDs and markers of bone turnover among the three treatment groups after 18 months TPTD treatment

Detailed description: We prospectively randomize 125 postmenopausal women after 9 months of TPTD treatment into three different open-label groups for another 9 months: either alendronate (ALN, 70 mg/week), raloxifene (RAL, 60 mg/day) or no medication (TPTD mono) on top of ongoing TPTD treatment. All subjects receive daily supplementation of 1000mg calcium and 800 IU vitamin D. Serum level of intact amino terminal propeptide of type I procollagen (PINP) and type 1 collagen cross-linked C-telopeptide (CTX) as well as DXA measurement at the spine, total hip and femoral neck BMD are evaluated at TPTD treatment initiation, at baseline of randomization to antiresorptive therapy as well as at 3 and 9 months during the combination treatment. Volumetric BMD values will be also determined.


Minimum age: 55 Years. Maximum age: 88 Years. Gender(s): Female.


Inclusion Criteria:

- Ambulatory postmenopausal women at least 55 years of age

- Patients with "unsatisfactory clinical response to previous antiresorptive therapy"

according to the national reimbursement criteria of Austria (either new clinical or radiographic fragility fracture on ≥ 2 years and/or accelerated bone loss of ≥ 3. 5%/year on antiresorptive treatment; discontinuation of oral antiresorptive treatment due to side-effects and substantial risk for osteoporotic fracture defined

by a T-Score ≤ - 2. 5 or ≥ 2 clinical risk factors according to the FRAX™-algorithm)and

consequently started with teriparatide treatment

- Patients treated with teriparatide (20 ug/day) currently and since 9 months for

postmenopausal osteoporosis

- Lumbar spine, femoral neck, and total hip evaluable by dual energy x ray

absorptiometry (DXA)

- Normal or clinically non-significant abnormal laboratory values (as defined by the


- Without language barrier, cooperative, expected to return for all follow-up

procedures, and who give informed consent before entering the study and after being informed of the medications and procedures to be used in this study Exclusion Criteria:

- History of bone metabolic diseases, Paget's disease, renal osteodystrophy,

osteomalacia, any secondary causes of osteoporosis, hyperparathyroidism (uncorrected), and intestinal malabsorption

- History of malignant neoplasms in the prior 5 years, with the exception of

superficial basal cell carcinoma or squamous cell carcinoma of the skin that has been definitively treated. If malignant neoplasm was ever diagnosed, patient must presently be free of disease

- History of nephrolithiasis or urolithiasis in the prior 2 years. Patients with any

documented history of nephro- or uro-lithiasis must have had an appropriate imaging procedure within the prior 6 months, such as, an intravenous pyleogram (IVP), supine radiograph of the kidney ureter bladder, or renal ultrasound, which must document the absence of stones

- Abnormal thyroid function at any time in the prior 6 months. Patients with chronic

hypothyreosis and adequate substitution therapy are permitted

- Active liver disease (liver enzymes more than three times the upper limit of normal)

or clinical jaundice

- Significantly impaired renal function. This is defined as serum creatinine >1. 8


- Treatment with bone active agent other than teriparatide in the prior 9 months

Locations and Contacts

Medical University of Vienna, Vienna 1060, Austria
Additional Information

Homepage of Medical Department II, Vienna (German)

Starting date: March 2006
Last updated: December 30, 2012

Page last updated: August 20, 2015

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