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EVA: Evista Alendronate Comparison

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00035971
Enrollment
Unknown
Registered
2002-05-08
Start date
Unknown
Completion date
Unknown
Last updated
2006-07-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoporosis

Brief summary

The purpose of this study is to determine how treatment with raloxifene compares to treatment with alendronate in postmenopausal women with osteoporosis on the chance of experiencing fractures

Interventions

DRUGraloxifene HCI and alendronate Na

Sponsors

Eli Lilly and Company
Lead SponsorINDUSTRY

Study design

Primary purpose
TREATMENT

Eligibility

Sex/Gender
FEMALE
Age
50 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* 50-80 years of age, inclusive * 2 years since last menses * Dx femoral neck osteoporosis * No vertebral fractures

Exclusion criteria

* Poor candidate for study drugs * Hx of diseases affecting bone metabolism * Hx of breast/estrogen-dependent cancer * Current use of osteoporosis drug therapy * Hx/high risk of VTE

Countries

Canada, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 8, 2026