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NCT01916850 · ClinicalTrials.gov registry record · Phase 1

Study to Determine the Safety, Tolerability and Pharmacokinetics Following Multiple Doses of LX4211 in Healthy Subjects

A Phase 1 study, sponsored by Lexicon Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
25
Enrollment target

NCT01916850: Completed Phase 1 study, sponsored by Lexicon Pharmaceuticals.

NCT01916850 is a Phase 1 study that has completed, run by Lexicon Pharmaceuticals. The registered enrollment target is 25 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01916850, a Phase 1 study, has completed, sponsored by Lexicon Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
25 participants
Enrollment target

Study Summary

The primary objective of this study is to evaluate the safety and tolerability of multiple oral doses of LX4211 400 mg and LX4211 800 mg (administered once daily for 10 consecutive days) in healthy subjects.

Interventions

  • DRUG LX4211 800 mg
  • DRUG LX4211 Placebo
  • DRUG LX4211 400 mg

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2013-08
Phase Phase 1
Lexicon Pharmaceuticals

56 total trials

What the finished NCT01916850 record still lists

NCT01916850 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower).

The record links to 0 conditions, and to 3 interventions - of which LX4211 800 mg is the first listed.

NCT01916850 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01916850 about?

NCT01916850 is a clinical study titled "Study to Determine the Safety, Tolerability and Pharmacokinetics Following Multiple Doses of LX4211 in Healthy Subjects". The primary objective of this study is to evaluate the safety and tolerability of multiple oral doses of LX4211 400 mg and LX4211 800 mg (administered once daily for 10 consecutive days) in healthy subjects.

What is the current status of trial NCT01916850?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2013-08.

What interventions are being tested in trial NCT01916850?

The interventions under investigation include: LX4211 800 mg (DRUG), LX4211 Placebo (DRUG), LX4211 400 mg (DRUG).

Who is sponsoring clinical trial NCT01916850?

This trial is sponsored by Lexicon Pharmaceuticals, which has 56 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01916850's enrollment target sits among peer trials

25 1495th of 2000 higher than 481 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 NCT01916850, the US trial registry maintained by the National Library of Medicine. NCT01916850 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.