Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01673178 · ClinicalTrials.gov registry record · Phase 1

Multiple Dose Study Of PF-05231023 In Adult Subjects Who Have Poor Lipid Control With And Without Type 2 Diabetes Mellitus

A Phase 1 study, sponsored by Pfizer.

Completed
Registry status
Phase 1
Development phase
107
Enrollment target

NCT01673178: Completed Phase 1 study, sponsored by Pfizer.

NCT01673178 is a Phase 1 study that has completed, run by Pfizer. The registered enrollment target is 107 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (78% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01673178, a Phase 1 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
107 participants
Enrollment target

Study Summary

This is a trial in obese subjects who have poor lipid control with and without Type 2 diabetes mellitus to study the safety, tolerability and pharmacokinetics of multiple doses of PF-05231023

Primary Outcome

An AE was any untoward medical occurrence in a participant who received study drug without regard to possibility of causal relationship. An SAE was an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged inpatient hospitalization; life-threatening experience (immediate risk of dying); persistent or significant disability/incapacity; congenital anomaly. Treatment-emergent events were between first dose of study drug and up to 28 day

Interventions

  • OTHER Placebo
  • DRUG 25 mg PF-05231023
  • DRUG 50 mg PF-05231023
  • DRUG 100 mg PF-05231023
  • DRUG 150 mg PF-05231023

Trial Details

FieldValue
Enrollment Target 107 participants
Start Date 2012-10
Est. Completion 2013-09
Phase Phase 1
Pfizer

1,845 total trials

What the finished NCT01673178 record still lists

NCT01673178 is an interventional study that assigns participants to a tested intervention. The registered 107 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 (78% higher).

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

NCT01673178 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01673178 about?

NCT01673178 is a clinical study titled "Multiple Dose Study Of PF-05231023 In Adult Subjects Who Have Poor Lipid Control With And Without Type 2 Diabetes Mellitus". This is a trial in obese subjects who have poor lipid control with and without Type 2 diabetes mellitus to study the safety, tolerability and pharmacokinetics of multiple doses of PF-05231023

What is the current status of trial NCT01673178?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 107 participants. The study started on 2012-10. Estimated completion is 2013-09.

What interventions are being tested in trial NCT01673178?

The interventions under investigation include: Placebo (OTHER), 25 mg PF-05231023 (DRUG), 50 mg PF-05231023 (DRUG), 100 mg PF-05231023 (DRUG), 150 mg PF-05231023 (DRUG).

Who is sponsoring clinical trial NCT01673178?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01673178's enrollment target sits among peer trials

107 531st of 2000 higher than 1,470 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05491668 · 107 participants

    Physiological Assessment of Severe Coronary Stenosis for Informing Planned PCI

  • NCT06041594 · 107 participants · NA

    Treating Pulmonary Embolism With Laguna Thrombectomy System (TRUST)

  • NCT06081426 · 107 participants · NA

    Examining Neurobiological Mechanisms Underlying the Therapeutic Effect of the Ketogenic Diet in Bipolar Disorder (BD)

  • NCT06527599 · 107 participants · NA

    Screening in Trauma for Opioid Misuse Prevention - an Adaptive Intervention

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01673178, the US trial registry maintained by the National Library of Medicine. NCT01673178 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.