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A First-in-human Study Evaluating AMG 785 in Healthy Men and Postmenopausal Women

2014-08-27 03:16:15 | BioPortfolio

Summary

The primary objective of this study is to assess the safety and tolerability of AMG 785 following a single dose subcutaneous (SC) or intravenous (IV) administration in healthy men and postmenopausal women.

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Conditions

Osteopenia

Intervention

AMG 785, Placebo

Status

Completed

Source

Amgen

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:16:15-0400

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