Phase 4
N=140
Efficacy and Safety of Brand Versus Generic Alendronate for Osteoporosis Treatment
Osteoporosis
Bottom Line
View on ClinicalTrials.gov: NCT02371252 ↗Enrolled (actual)
140
Serious AEs
2.1%
Results posted
Sep 2021
Primary outcome: Primary: Bone Mineral Density (BMD) at Lumbar Spine (L1-L4) — 5.54; 5.39 percent
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 4
- Interventions
- Generic alendronate (Drug)
- Age
- Adult, Older Adult · 50+ yrs
- Sex
- All
- Sponsor
- Mahidol University
- Primary completion
- Dec 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Bone Mineral Density (BMD) at Lumbar Spine (L1-L4) |
5.54; 5.39 | — |
| SECONDARY Bone Mineral Density (BMD) at Total Hip |
2.48; 2.52 | — |
| SECONDARY Bone Resorption Markers (Serum CTX) |
— | — |
| SECONDARY Bone Formation Marker (Serum PINP) |
— | — |
Summary
Osteoporosis is a common disease defined as a decrease in bone mass and strength which increases risk of fragility fractures. This disorder may affecting health in many adults which causing disability, morbidity, and mortality. Current first-line medical therapy is bisphosphonates which alendronate is one of the most widely used. However, expenditure on medicines is one of the major problem of inadequate access to treatment.
The investigators hypothesized that generic alendronate will have the same clinical efficacy as the brand formulation. Therefore, the result of this study is extremely crucial. If adequate efficacy of generic alendronate could be established and if it affords the same safety profile as those of brand alendronate, the use of generic alendronate could then be recommended.
Eligibility Criteria
Inclusion Criteria: patients who are postmenopausal women or men who aged older than 50 years and meet the indications for osteoporosis treatment according to the Thai Osteoporosis Foundation's 2010 treatment guidelines.
- History of spinal or hip fractures with low energy trauma.
- BMD by Dual energy X-ray absorptiometry (DXA) scan with T-score ≤ -2.5 at the femoral neck, total hip, or L1-L4 spine.
- BMD by DXA scan with T-score between -1 and -2.5 at the femoral neck, total hip, or L1-L4 spine and a 10-year hip fracture probability ≥ 3% or a 10-year major osteoporosis-related fracture probability ≥ 20% based on Fracture risk assessment tool (FRAX)
Exclusion Criteria
- Patients who have contraindications to use bisphosphonates e.g. gastroesophageal reflux disease or drug allergy to bisphosphonates
- Patients with an abnormality of serum calcium levels (more than 10.2 mg/dl or less than 8.7 mg/dl)
- Patients with estimated glomerular filtration rate less than 30 mL/min/1.73 m2
- Patients with metabolic bone diseases such as Paget's disease, hyperparathyroidism, etc.
- Patients who were received anti-osteoporotic drugs during the past 1 year.
- Patients who currently taking steroids, hormone replacement therapy, or selective estrogen receptor modulators (SERMs) within 1 year.
Data sourced from ClinicalTrials.gov (NCT02371252). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.