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NCT01488877 · ClinicalTrials.gov registry record · Phase 1

A Study To Evaluate The Safety And Tolerability Of PF-03882845 In Patients With Type 2 Diabetic Nephropathy

A Phase 1 study, sponsored by Pfizer.

Terminated
Registry status
Phase 1
Development phase
6
Enrollment target

NCT01488877: Clinical Trial Phase 1 study, sponsored by Pfizer.

NCT01488877 is a Phase 1 study that was terminated before completion, run by Pfizer. The registered enrollment target is 6 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01488877, a Phase 1 study, was terminated before completion, sponsored by Pfizer.

TERMINATED
Registry status
Phase 1
Development phase
6 participants
Enrollment target

Study Summary

PF-03882845 is a compound proposed for treatment of type 2 diabetic nephropathy. The primary purpose of this trial is to evaluate the safety and tolerability, pharmacokinetics and pharmacodynamics of multiple doses of PF-03882845 in this population.

Primary Outcome

Baseline value calculated as the average of -24 hours (pre-dose) measurement on Day -1 and 0 hours (immediately pre-dose) measurement on Day 1. Day 8 value calculated was average of 0 hours (immediately pre-dose) measurements on Day 7 and 8. Change from baseline values were presented under time point of Day 8.

Interventions

  • DRUG Spironolactone
  • OTHER placebo
  • DRUG PF-03882845

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2012-01
Est. Completion 2012-07
Phase Phase 1
Pfizer

1,845 total trials

Why NCT01488877 stopped before completion

NCT01488877 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower).

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

NCT01488877 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01488877 about?

NCT01488877 is a clinical study titled "A Study To Evaluate The Safety And Tolerability Of PF-03882845 In Patients With Type 2 Diabetic Nephropathy". PF-03882845 is a compound proposed for treatment of type 2 diabetic nephropathy. The primary purpose of this trial is to evaluate the safety and tolerability, pharmacokinetics and pharmacodynamics of multiple doses of PF-03882845 in this population.

What is the current status of trial NCT01488877?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 6 participants. The study started on 2012-01. Estimated completion is 2012-07.

What interventions are being tested in trial NCT01488877?

The interventions under investigation include: Spironolactone (DRUG), placebo (OTHER), PF-03882845 (DRUG).

Who is sponsoring clinical trial NCT01488877?

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 NCT01488877's enrollment target sits among peer trials

6 1974th of 2000 higher than 12 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 NCT01488877, the US trial registry maintained by the National Library of Medicine. NCT01488877 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.