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NCT02055157 · ClinicalTrials.gov registry record · Phase 2

A Phase 2 Study of BMN 111 to Evaluate Safety, Tolerability, and Efficacy in Children With Achondroplasia

A Phase 2 study, sponsored by BioMarin Pharmaceutical.

Completed
Registry status
Phase 2
Development phase
35
Enrollment target

NCT02055157: Completed Phase 2 study, sponsored by BioMarin Pharmaceutical.

NCT02055157 is a Phase 2 study that has completed, run by BioMarin Pharmaceutical. The registered enrollment target is 35 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (74% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02055157, a Phase 2 study, has completed, sponsored by BioMarin Pharmaceutical.

COMPLETED
Registry status
Phase 2
Development phase
35 participants
Enrollment target

Study Summary

This is a Phase 2, open-label, sequential cohort dose-escalation study of BMN 111 in children with achondroplasia. The primary objective is to assess the safety and tolerability of daily BMN 111 administered to children with achondroplasia.

Primary Outcome

A treatment-emergent Adverse Events (TEAE) is any Adverse Events that newly appeared, increased in frequency or worsened in severity following initiation of study drug administration. Serious adverse event (SAE).

Interventions

  • DRUG BMN 111

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2014-01-13
Est. Completion 2017-10-02
Phase Phase 2
BioMarin Pharmaceutical

80 total trials

What the finished NCT02055157 record still lists

NCT02055157 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 35 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (74% lower).

The record links to 0 conditions, and to 1 intervention - of which BMN 111 is the first listed.

NCT02055157 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02055157 about?

NCT02055157 is a clinical study titled "A Phase 2 Study of BMN 111 to Evaluate Safety, Tolerability, and Efficacy in Children With Achondroplasia". This is a Phase 2, open-label, sequential cohort dose-escalation study of BMN 111 in children with achondroplasia. The primary objective is to assess the safety and tolerability of daily BMN 111 administered to children with achondroplasia.

What is the current status of trial NCT02055157?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 35 participants. The study started on 2014-01-13. Estimated completion is 2017-10-02.

What interventions are being tested in trial NCT02055157?

The interventions under investigation include: BMN 111 (DRUG).

Who is sponsoring clinical trial NCT02055157?

This trial is sponsored by BioMarin Pharmaceutical, which has 80 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02055157's enrollment target sits among peer trials

35 1524th of 2000 higher than 462 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02055157, the US trial registry maintained by the National Library of Medicine. NCT02055157 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.