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Bioequivalence Study to Compare Two Injection Devices for BMN 111 in Healthy Participants

Achondroplasia Clinical Trial

Official title:
A Phase 1, Randomized, Open-Label, Sponsor-Open, Two-Sequence, Two-Period Crossover Study to Investigate the Bioequivalence of a Single Subcutaneous Dose of BMN 111 Administered Using Either a Vial and Syringe or Injector Pen in Healthy Adult Participants

Clinical Trial Summary

The purpose of this study is to establish the bioequivalence of a single SC dose of BMN 111 administered using a vial and syringe versus using an injector pen.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05813314
Study type Interventional
Source BioMarin Pharmaceutical
Contact
Status Terminated
Phase Phase 1
Start date March 15, 2023
Completion date June 14, 2023
View Details
See also
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