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NCT02159066 · ClinicalTrials.gov registry record · Phase 2

LGX818 and MEK162 in Combination With a Third Agent (BKM120, LEE011, BGJ398 or INC280) in Advanced BRAF Melanoma

A Phase 2 study, sponsored by Pfizer.

Completed
Registry status
Phase 2
Development phase
158
Enrollment target

NCT02159066: Completed Phase 2 study, sponsored by Pfizer.

NCT02159066 is a Phase 2 study that has completed, run by Pfizer. The registered enrollment target is 158 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (19% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02159066, a Phase 2 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 2
Development phase
158 participants
Enrollment target

Study Summary

The primary purpose of this study is to assess the anti-tumor activity of LGX818/MEK162 in combination with targeted agents after progression on LGX818/MEK162 combination therapy, as well as the safety and tolerability of the novel triple combinations.

Primary Outcome

ORR: percentage of participants with confirmed complete response (CR) and partial response (PR). Response evaluation criteria in solid tumors (RECIST) v1.1: a) CR = disappearance of all non-nodal target lesions. In addition, any pathological lymph nodes assigned as target lesions that had a reduction in short axis to less than (\<) 10 millimeter (mm). Disappearance of all non-target lesions. In addition, all lymph nodes assigned a non-target lesion must be non-pathological in size (\<10 mm short

Interventions

  • DRUG LEE011
  • DRUG MEK162
  • DRUG LGX818
  • DRUG BKM120
  • DRUG BGJ398

Trial Details

FieldValue
Enrollment Target 158 participants
Start Date 2014-07-23
Est. Completion 2023-01-10
Phase Phase 2
Pfizer

1,845 total trials

What the finished NCT02159066 record still lists

NCT02159066 is an interventional study that assigns participants to a tested intervention. The registered 158 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (19% higher).

The record links to 0 conditions, and to 5 interventions - of which LEE011 is the first listed.

NCT02159066 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02159066 about?

NCT02159066 is a clinical study titled "LGX818 and MEK162 in Combination With a Third Agent (BKM120, LEE011, BGJ398 or INC280) in Advanced BRAF Melanoma". The primary purpose of this study is to assess the anti-tumor activity of LGX818/MEK162 in combination with targeted agents after progression on LGX818/MEK162 combination therapy, as well as the safety and tolerability of the novel triple combinations.

What is the current status of trial NCT02159066?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 158 participants. The study started on 2014-07-23. Estimated completion is 2023-01-10.

What interventions are being tested in trial NCT02159066?

The interventions under investigation include: LEE011 (DRUG), MEK162 (DRUG), LGX818 (DRUG), BKM120 (DRUG), BGJ398 (DRUG).

Who is sponsoring clinical trial NCT02159066?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02159066's enrollment target sits among peer trials

158 443rd of 2000 higher than 1,558 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 NCT02159066, the US trial registry maintained by the National Library of Medicine. NCT02159066 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.