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NCT01428427 · ClinicalTrials.gov registry record · Phase 1

Combination Study of GSK1120212 With Gemcitabine in Subjects With Solid Tumors

A Phase 1 study, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 1
Development phase
31
Enrollment target

NCT01428427: Completed Phase 1 study, sponsored by GlaxoSmithKline.

NCT01428427 is a Phase 1 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 31 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (48% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01428427, a Phase 1 study, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 1
Development phase
31 participants
Enrollment target

Study Summary

MEK112111 is a dose-escalation, Phase IB, open-label, single-arm, multi-center study. The primary objective of the study is to determine the recommended dose and regimen for the orally administered MEK inhibitor GSK1120212 dosed in combination with gemcitabine in subjects with solid tumors.

Interventions

  • DRUG Gemcitabine
  • DRUG GSK1120212

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2009-08-12
Est. Completion 2011-07-18
Phase Phase 1
GlaxoSmithKline

1,345 total trials

What the finished NCT01428427 record still lists

NCT01428427 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (48% lower).

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

NCT01428427 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01428427 about?

NCT01428427 is a clinical study titled "Combination Study of GSK1120212 With Gemcitabine in Subjects With Solid Tumors". MEK112111 is a dose-escalation, Phase IB, open-label, single-arm, multi-center study. The primary objective of the study is to determine the recommended dose and regimen for the orally administered MEK inhibitor GSK1120212 dosed in combination with gemcitabine in subjects with solid tumors.

What is the current status of trial NCT01428427?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 31 participants. The study started on 2009-08-12. Estimated completion is 2011-07-18.

What interventions are being tested in trial NCT01428427?

The interventions under investigation include: Gemcitabine (DRUG), GSK1120212 (DRUG).

Who is sponsoring clinical trial NCT01428427?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01428427's enrollment target sits among peer trials

31 1322nd of 2000 higher than 669 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 NCT01428427, the US trial registry maintained by the National Library of Medicine. NCT01428427 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.