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NCT01626573 · ClinicalTrials.gov registry record · Phase 2

A Study Exploring the Safety, Tolerability, and Efficacy of a 28 Day Course Followed by an Additional 56 Day Course of Itacitinib in Subjects With Active Rheumatoid Arthritis

A Phase 2 study, sponsored by Incyte Corporation.

Completed
Registry status
Phase 2
Development phase
106
Enrollment target

NCT01626573: Completed Phase 2 study, sponsored by Incyte Corporation.

NCT01626573 is a Phase 2 study that has completed, run by Incyte Corporation. The registered enrollment target is 106 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01626573, a Phase 2 study, has completed, sponsored by Incyte Corporation.

COMPLETED
Registry status
Phase 2
Development phase
106 participants
Enrollment target

Study Summary

This is a study evaluating a 28-day course followed by a 56-day course of itacitinib in patients with active rheumatoid arthritis (RA). The study will evaluate safety and efficacy parameters of itacitinib.

Interventions

  • DRUG Itacitinib
  • DRUG Itacitinib Placebo

Trial Details

FieldValue
Enrollment Target 106 participants
Start Date 2012-03
Est. Completion 2013-10
Phase Phase 2
Incyte Corporation

239 total trials

What the finished NCT01626573 record still lists

NCT01626573 is an interventional study that assigns participants to a tested intervention. The registered 106 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% lower).

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

NCT01626573 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01626573 about?

NCT01626573 is a clinical study titled "A Study Exploring the Safety, Tolerability, and Efficacy of a 28 Day Course Followed by an Additional 56 Day Course of Itacitinib in Subjects With Active Rheumatoid Arthritis". This is a study evaluating a 28-day course followed by a 56-day course of itacitinib in patients with active rheumatoid arthritis (RA). The study will evaluate safety and efficacy parameters of itacitinib.

What is the current status of trial NCT01626573?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 106 participants. The study started on 2012-03. Estimated completion is 2013-10.

What interventions are being tested in trial NCT01626573?

The interventions under investigation include: Itacitinib (DRUG), Itacitinib Placebo (DRUG).

Who is sponsoring clinical trial NCT01626573?

This trial is sponsored by Incyte Corporation, which has 239 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01626573's enrollment target sits among peer trials

106 648th of 2000 higher than 1,351 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 NCT01626573, the US trial registry maintained by the National Library of Medicine. NCT01626573 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.