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NCT02672839 · ClinicalTrials.gov registry record · Phase 1

A Comparison Study of the Bioavailability of a Capsule Formulation of LGD-6972 to an Oral Solution Formulation

A Phase 1 study, sponsored by Ligand Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
12
Enrollment target

NCT02672839: Completed Phase 1 study, sponsored by Ligand Pharmaceuticals.

NCT02672839 is a Phase 1 study that has completed, run by Ligand Pharmaceuticals. The registered enrollment target is 12 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02672839, a Phase 1 study, has completed, sponsored by Ligand Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
12 participants
Enrollment target

Study Summary

The purpose of this study is to compare relative oral bioavailability of a capsule formulation of LGD-6972 to a solution formulation of LGD-6972.

Primary Outcome

AUC: ratio: medium test form to reference form

Interventions

  • DRUG LGD-6972 Solution
  • DRUG LGD-6972 Capsules

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2016-02
Est. Completion 2016-05
Phase Phase 1
Ligand Pharmaceuticals

15 total trials

What the finished NCT02672839 record still lists

NCT02672839 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower).

The record links to 0 conditions, and to 2 interventions - of which LGD-6972 Solution is the first listed.

NCT02672839 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02672839 about?

NCT02672839 is a clinical study titled "A Comparison Study of the Bioavailability of a Capsule Formulation of LGD-6972 to an Oral Solution Formulation". The purpose of this study is to compare relative oral bioavailability of a capsule formulation of LGD-6972 to a solution formulation of LGD-6972.

What is the current status of trial NCT02672839?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2016-02. Estimated completion is 2016-05.

What interventions are being tested in trial NCT02672839?

The interventions under investigation include: LGD-6972 Solution (DRUG), LGD-6972 Capsules (DRUG).

Who is sponsoring clinical trial NCT02672839?

This trial is sponsored by Ligand Pharmaceuticals, which has 15 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02672839's enrollment target sits among peer trials

12 1852nd of 2000 higher than 90 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 NCT02672839, the US trial registry maintained by the National Library of Medicine. NCT02672839 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.