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NCT01607385 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Safety, Tolerability, Pharmacokinetic a Single Day of Dosing With GSK1614235.

A Phase 1 study, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 1
Development phase
56
Enrollment target

NCT01607385: Completed Phase 1 study, sponsored by GlaxoSmithKline.

NCT01607385 is a Phase 1 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 56 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01607385, a Phase 1 study, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 1
Development phase
56 participants
Enrollment target

Study Summary

A single blind, randomized, placebo-controlled, dose escalating study to evaluate the safety, tolerability, pharmacokinetic and pharmacodynamic parameters of repeat doses of GSK2330672 in healthy volunteers, given alone and with a single day of dosing with GSK1614235

Interventions

  • DRUG Placebo
  • DRUG GSK2330672
  • DRUG GSK1614235

Trial Details

FieldValue
Enrollment Target 56 participants
Start Date 2012-05-18
Est. Completion 2012-12-03
Phase Phase 1
GlaxoSmithKline

1,345 total trials

What the finished NCT01607385 record still lists

NCT01607385 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 56 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT01607385 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01607385 about?

NCT01607385 is a clinical study titled "A Study to Evaluate the Safety, Tolerability, Pharmacokinetic a Single Day of Dosing With GSK1614235.". A single blind, randomized, placebo-controlled, dose escalating study to evaluate the safety, tolerability, pharmacokinetic and pharmacodynamic parameters of repeat doses of GSK2330672 in healthy volunteers, given alone and with a single day of dosing with GSK1614235

What is the current status of trial NCT01607385?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 56 participants. The study started on 2012-05-18. Estimated completion is 2012-12-03.

What interventions are being tested in trial NCT01607385?

The interventions under investigation include: Placebo (DRUG), GSK2330672 (DRUG), GSK1614235 (DRUG).

Who is sponsoring clinical trial NCT01607385?

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 NCT01607385's enrollment target sits among peer trials

56 902nd of 2000 higher than 1,083 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 NCT01607385, the US trial registry maintained by the National Library of Medicine. NCT01607385 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.