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Clinical Trials/NL-OMON32748
NL-OMON32748
Completed
Not Applicable

A phase 1 double blind, placebo controlled study of ALX-0141 single dose subcutaneous administration in healthy post-menopausal women - ALX-0141 s.c. SAD study

Ablynx N.V.0 sites42 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bone loss
Sponsor
Ablynx N.V.
Enrollment
42
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Ablynx N.V.

Eligibility Criteria

Inclusion Criteria

  • Healthy post menopausal women, 18 \- 80 years old, BMI between 18 and 36 kg/m2, moderate or non\-smoker.

Exclusion Criteria

  • Suffering from: hepatitis B, cancer or HIV/AIDS. In case of participation in another drug study within 60 days before the start of this study or being a blood donor within 60 days from the start of the study. In case of donating more than 1\.0 liters of blood in the 10 months prior the start of this study.

Outcomes

Primary Outcomes

Not specified

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