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NCT01010542 · ClinicalTrials.gov registry record · Phase 1

Study Evaluating Single Dose Of ILV-095 In Psoriasis Subjects

A Phase 1 study, sponsored by Pfizer.

Terminated
Registry status
Phase 1
Development phase
39
Enrollment target

NCT01010542: Clinical Trial Phase 1 study, sponsored by Pfizer.

NCT01010542 is a Phase 1 study that was terminated before completion, run by Pfizer. The registered enrollment target is 39 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (35% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01010542, a Phase 1 study, was terminated before completion, sponsored by Pfizer.

TERMINATED
Registry status
Phase 1
Development phase
39 participants
Enrollment target

Study Summary

The purpose of this research study is to evaluate the safety and tolerability of ILV-095 when it is given to individuals with moderate to severe chronic plaque psoriasis. Another purpose of the study is to observe how the drug enters the blood and tissues over time, how the body breaks down the drug and whether or not the body will develop an immune reaction (sensitivity) to the drug.

Primary Outcome

PASI score: combined assessment of lesion severity and area affected into single score range:0 (no disease) to 72(maximal disease),with higher scores representing greater severity of psoriasis.Body divided into 4 sections(head and neck \[h\],arms \[u\],trunk \[t\],legs \[l\]);each area scored by itself and scores combined for final PASI score.For each section,percent body surface area(A) of skin involved was estimated:0 (no involvement) to 6 (90 to 100 percent involvement),severity estimated by

Interventions

  • DRUG ILV-095 300 mg in a 4 to 1 ratio

Trial Details

FieldValue
Enrollment Target 39 participants
Start Date 2009-12-01
Est. Completion 2011-05-20
Phase Phase 1
Pfizer

1,845 total trials

Why NCT01010542 stopped before completion

NCT01010542 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 39 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (35% lower).

The record links to 0 conditions, and to 1 intervention - of which ILV-095 300 mg in a 4 to 1 ratio is the first listed.

NCT01010542 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01010542 about?

NCT01010542 is a clinical study titled "Study Evaluating Single Dose Of ILV-095 In Psoriasis Subjects". The purpose of this research study is to evaluate the safety and tolerability of ILV-095 when it is given to individuals with moderate to severe chronic plaque psoriasis. Another purpose of the study is to observe how the drug enters the blood and tissues over time, how the body breaks down the drug...

What is the current status of trial NCT01010542?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 39 participants. The study started on 2009-12-01. Estimated completion is 2011-05-20.

What interventions are being tested in trial NCT01010542?

The interventions under investigation include: ILV-095 300 mg in a 4 to 1 ratio (DRUG).

Who is sponsoring clinical trial NCT01010542?

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 NCT01010542's enrollment target sits among peer trials

39 1191st of 2000 higher than 804 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 NCT01010542, the US trial registry maintained by the National Library of Medicine. NCT01010542 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.