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NCT01192165 · ClinicalTrials.gov registry record · Phase 1

Safety and Tolerability Study of GSK1120212, a MEK Inhibitor, in Combination With Docetaxel, Erlotinib, Pemetrexed, Pemetrexed + Carboplatin, Pemetrexed + Cisplatin, or Nab-Paclitaxel

A Phase 1 study, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 1
Development phase
169
Enrollment target

NCT01192165: Completed Phase 1 study, sponsored by GlaxoSmithKline.

NCT01192165 is a Phase 1 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 169 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (182% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01192165, a Phase 1 study, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 1
Development phase
169 participants
Enrollment target

Study Summary

The purpose of this study is to determine what dose of GSK1120212 can be given safely in combination with at least one other drug that is already approved to treat cancer. This study will test the safety of up to 6 different GSK1120212 study treatment combinations (GSK1120212 plus either docetaxel, erlotinib, pemetrexed, pemetrexed + carboplatin, pemetrexed + cisplatin, or nab-paclitaxel). The doses identified in this study may be used in future trials to test whether the combination treatment is a safe and effective therapy for subjects with metastatic lung and/or pancreatic cancers.

Interventions

  • DRUG Carboplatin
  • DRUG Docetaxel
  • DRUG Pemetrexed
  • DRUG Erlotinib
  • DRUG Trametinib (GSK1120212)

Trial Details

FieldValue
Enrollment Target 169 participants
Start Date 2010-09-14
Est. Completion 2013-10-07
Phase Phase 1
GlaxoSmithKline

1,345 total trials

What the finished NCT01192165 record still lists

NCT01192165 is an interventional study that assigns participants to a tested intervention. The registered 169 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (182% higher).

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

NCT01192165 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01192165 about?

NCT01192165 is a clinical study titled "Safety and Tolerability Study of GSK1120212, a MEK Inhibitor, in Combination With Docetaxel, Erlotinib, Pemetrexed, Pemetrexed + Carboplatin, Pemetrexed + Cisplatin, or Nab-Paclitaxel". The purpose of this study is to determine what dose of GSK1120212 can be given safely in combination with at least one other drug that is already approved to treat cancer. This study will test the safety of up to 6 different GSK1120212 study treatment combinations (GSK1120212 plus either docetaxel, ...

What is the current status of trial NCT01192165?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 169 participants. The study started on 2010-09-14. Estimated completion is 2013-10-07.

What interventions are being tested in trial NCT01192165?

The interventions under investigation include: Carboplatin (DRUG), Docetaxel (DRUG), Pemetrexed (DRUG), Erlotinib (DRUG), Trametinib (GSK1120212) (DRUG).

Who is sponsoring clinical trial NCT01192165?

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 NCT01192165's enrollment target sits among peer trials

169 326th of 2000 higher than 1,675 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 NCT01192165, the US trial registry maintained by the National Library of Medicine. NCT01192165 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.