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NCT02273219 · ClinicalTrials.gov registry record · Phase 1

Trial of AEB071 in Combination With BYL719 in Patients With Melanoma

A Phase 1 study, sponsored by Columbia University.

Completed
Registry status
Phase 1
Development phase
30
Enrollment target

NCT02273219: Completed Phase 1 study, sponsored by Columbia University.

NCT02273219 is a Phase 1 study that has completed, run by Columbia University. The registered enrollment target is 30 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02273219, a Phase 1 study, has completed, sponsored by Columbia University.

COMPLETED
Registry status
Phase 1
Development phase
30 participants
Enrollment target

Study Summary

Primary objective is to define the maximum tolerated dose (MTD) for the combination of AEB071 and BYL719. Secondary objectives are to define the safety and tolerability of AEB071 and BYL719.

Primary Outcome

Establish the maximum tolerated dose (up to 400 mg twice daily) for AEB071 and up to 350 mg daily for BYL719

Interventions

  • DRUG BYL719
  • DRUG AEB071

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2014-11-19
Est. Completion 2018-07-02
Phase Phase 1
Columbia University

958 total trials

What the finished NCT02273219 record still lists

NCT02273219 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower).

The record links to 0 conditions, and to 2 interventions - of which BYL719 is the first listed.

NCT02273219 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02273219 about?

NCT02273219 is a clinical study titled "Trial of AEB071 in Combination With BYL719 in Patients With Melanoma". Primary objective is to define the maximum tolerated dose (MTD) for the combination of AEB071 and BYL719. Secondary objectives are to define the safety and tolerability of AEB071 and BYL719.

What is the current status of trial NCT02273219?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2014-11-19. Estimated completion is 2018-07-02.

What interventions are being tested in trial NCT02273219?

The interventions under investigation include: BYL719 (DRUG), AEB071 (DRUG).

Who is sponsoring clinical trial NCT02273219?

This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02273219's enrollment target sits among peer trials

30 1332nd of 2000 higher than 561 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT02273219, the US trial registry maintained by the National Library of Medicine. NCT02273219 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.