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NCT01592240 · ClinicalTrials.gov registry record · Phase 2

Monthly And Twice Monthly Subcutaneous Dosing Of PF-04950615 (RN316) In Hypercholesterolemic Subjects On A Statin

A Phase 2 study, sponsored by Pfizer.

Completed
Registry status
Phase 2
Development phase
354
Enrollment target

NCT01592240: Completed Phase 2 study, sponsored by Pfizer.

NCT01592240 is a Phase 2 study that has completed, run by Pfizer. The registered enrollment target is 354 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (166% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01592240, a Phase 2 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 2
Development phase
354 participants
Enrollment target

Study Summary

To evaluate the Low Density Lipoprotein-Cholesterol (LDL-C) lowering effect of PF-04950615 administered subcutaneously at monthly intervals, or twice monthly intervals in subjects with high cholesterol whose LDL-cholesterol is \>/=80 mg/dL on background treatment with a statin.

Interventions

  • DRUG PBO
  • DRUG 200mg PF-04950615 (RN316)
  • DRUG 300mg PF-04950615 (RN316)
  • DRUG PF-04950615

Trial Details

FieldValue
Enrollment Target 354 participants
Start Date 2012-07
Est. Completion 2013-05
Phase Phase 2
Pfizer

1,845 total trials

What the finished NCT01592240 record still lists

NCT01592240 is an interventional study that assigns participants to a tested intervention. The registered 354 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (166% higher).

The record links to 0 conditions, and to 4 interventions - of which PBO is the first listed.

NCT01592240 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01592240 about?

NCT01592240 is a clinical study titled "Monthly And Twice Monthly Subcutaneous Dosing Of PF-04950615 (RN316) In Hypercholesterolemic Subjects On A Statin". To evaluate the Low Density Lipoprotein-Cholesterol (LDL-C) lowering effect of PF-04950615 administered subcutaneously at monthly intervals, or twice monthly intervals in subjects with high cholesterol whose LDL-cholesterol is \>/=80 mg/dL on background treatment with a statin.

What is the current status of trial NCT01592240?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 354 participants. The study started on 2012-07. Estimated completion is 2013-05.

What interventions are being tested in trial NCT01592240?

The interventions under investigation include: PBO (DRUG), 200mg PF-04950615 (RN316) (DRUG), 300mg PF-04950615 (RN316) (DRUG), PF-04950615 (DRUG).

Who is sponsoring clinical trial NCT01592240?

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 NCT01592240's enrollment target sits among peer trials

354 128th of 2000 higher than 1,872 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT01592240, the US trial registry maintained by the National Library of Medicine. NCT01592240 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.