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NCT01262963 · ClinicalTrials.gov registry record · Phase 1

An Absorption, Distribution, Metabolism and Excretion (ADME) Study of Single Oral Dose [14C] GSK2118436 in Subjects With BRAF Mutant Solid Tumors

A Phase 1 study, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 1
Development phase
4
Enrollment target

NCT01262963: Completed Phase 1 study, sponsored by GlaxoSmithKline.

NCT01262963 is a Phase 1 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 4 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01262963, a Phase 1 study, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 1
Development phase
4 participants
Enrollment target

Study Summary

The study is a Phase 1, open-label study designed to characterize the absorption, distribution, metabolism and excretion of GSK2118436 following administration of a single oral 14C labeled dose of GSK2118436 as a suspension in subjects with BRAF mutation positive tumors.

Interventions

  • DRUG GSK2118436

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2011-01-26
Est. Completion 2011-04-08
Phase Phase 1
GlaxoSmithKline

1,345 total trials

What the finished NCT01262963 record still lists

NCT01262963 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 4 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (93% lower).

The record links to 0 conditions, and to 1 intervention - of which GSK2118436 is the first listed.

NCT01262963 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01262963 about?

NCT01262963 is a clinical study titled "An Absorption, Distribution, Metabolism and Excretion (ADME) Study of Single Oral Dose [14C] GSK2118436 in Subjects With BRAF Mutant Solid Tumors". The study is a Phase 1, open-label study designed to characterize the absorption, distribution, metabolism and excretion of GSK2118436 following administration of a single oral 14C labeled dose of GSK2118436 as a suspension in subjects with BRAF mutation positive tumors.

What is the current status of trial NCT01262963?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 4 participants. The study started on 2011-01-26. Estimated completion is 2011-04-08.

What interventions are being tested in trial NCT01262963?

The interventions under investigation include: GSK2118436 (DRUG).

Who is sponsoring clinical trial NCT01262963?

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 NCT01262963's enrollment target sits among peer trials

4 1995th of 2000 higher than 2 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 NCT01262963, the US trial registry maintained by the National Library of Medicine. NCT01262963 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.