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Controlled Study of ONO-5920 in Patients With Involutional Osteoporosis in Japan

Ono Pharmaceuticals logo

Ono Pharmaceuticals

Status and phase

Completed
Phase 3

Conditions

Involutional Osteoporosis

Treatments

Drug: ONO-5920

Study type

Interventional

Funder types

Industry

Identifiers

NCT00212719
ONO-5920-03

Details and patient eligibility

About

The purpose of this study is to evaluate the efficacy and safety of ONO-5920 in patients with involutional osteoporosis.

Sex

Female

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. A diagnosis in accordance with Criteria for the Diagnosis of Primary Osteoporosis.
  2. Other inclusion criteria as specified in the study protocol.

Exclusion criteria

  1. Patients having secondary osteoporosis or another condition that presents low bone mass.
  2. Patients having findings that affect measurement of lumbar spinal bone mineral density by DXA
  3. Patients that have been administered bisphosphonate derivatives.
  4. Other exclusion criteria as specified in the study protocol.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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