Phase 3 Psoriasis Trial, Completed NCT01186744 Sponsor: Pfizer Condition: Psoriasis
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Trial results

AI generated results summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

According to the results reported on ClinicalTrials.gov, this trial enrolled 666 participants in total across several groups, all of whom had psoriasis. The trial was testing a medicine called CP-690,550 (also known as tofacitinib) at two different doses — 5 mg and 10 mg, taken twice daily. The study was designed in three phases: an initial treatment period (Period A), a withdrawal period where some participants were switched to a dummy tablet called a placebo (Period B), and a re-treatment period (Period C). The trial measured how participants' psoriasis responded using two scoring tools — the PASI score (a detailed measure of how much of the body is affected and how severe the patches are) and the PGA score (a doctor's overall rating from "clear" to "severe"). The reported data shows that during the withdrawal phase (Period B), among those who had been on the 5 mg dose, around 90% who stayed on the medicine still met the PASI75 response threshold (meaning their psoriasis score had dropped by at least 75% from the start) at an early time point, compared with about 63% of those switched to placebo; by a later time point in that period, those figures had dropped to roughly 63% and 32% respectively. Similar patterns were reported for the 10 mg group. For the doctor's overall rating (PGA), the reported data shows that around 81% of those continuing on 5 mg were rated "clear" or "almost clear" at an early point in Period B, compared with about 57% on placebo; for the 10 mg group the figures were approximately 80% versus 52%. The reported data also shows that during re-treatment (Period C), participants who had previously been on the 10 mg dose and were then switched back after a break reached response thresholds at higher rates over time than those re-starting the 5 mg dose. For the secondary outcomes, the median time reported to reach the PASI75 threshold during the first treatment period was approximately 24.3 weeks for the 5 mg group and 8.7 weeks for the 10 mg group; similarly, the median time to a "clear" or "almost clear" doctor rating was about 24.1 weeks for the 5 mg group and 8.1 weeks for the 10 mg group. These are the results as reported to ClinicalTrials.gov. They are not medical advice — always discuss what they mean for you with your doctor.

These are the results as reported to ClinicalTrials.gov, not medical advice. Verify independently with the trial site and discuss what they mean for you with your doctor.

Phase 3 Psoriasis Trial, Completed

NCT01186744
Completed Phase 3 🇦🇺 Australian site

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

"Who might be able to join this trial:

  • You are 18 years old or older and have been diagnosed with the most common form of psoriasis (called plaque psoriasis) for at least 12 months before starting the study
  • Your psoriasis has been rated as moderate or severe by a doctor, based on standard scoring measurements
  • Your psoriasis covers at least 10% of your body surface area
  • You do not have an active, hidden, or untreated tuberculosis infection or other serious infections

Who may not be able to join:

  • You have a less common type of psoriasis, or your psoriasis was caused by a medication
  • You are unable to stop your current psoriasis treatments, including tablets, injections, creams, or light therapy, before and during the trial
  • You have any serious medical condition that is not well controlled (confirm with trial site)

Important: Always verify eligibility with the trial site directly before applying."

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Pfizer CT.gov Call Center, Pfizer

Australian sites

Dr. Glenn & Partners, Kogarah, New South Wales
Premier Dermatology, Kogarah, New South Wales
Skin and Cancer Foundation, Carlton, Victoria
Uniradiology, Carlton, Victoria
Malvern Diagnostic Imaging, Malvern, Victoria
Emeritus Research, Malvern East, Victoria

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Completed
Phase
Phase 3
Sponsor
Registry
ClinicalTrials.gov
Start date
1 September 2010
Est. completion
1 January 2013

Where this trial is recruiting

🇦🇷 Argentina 🇦🇺 Australia 🇧🇷 Brazil 🇧🇬 Bulgaria 🇨🇦 Canada 🇩🇰 Denmark 🇫🇮 Finland 🇬🇷 Greece 🇳🇱 Netherlands 🇸🇰 Slovakia 🇬🇧 United Kingdom 🇺🇸 United States

6 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Percentage of Participants Maintaining a Psoriasis Area and Severity Index 75 (PASI75) Response During the Double-Blind Treatment Withdrawal Period (Period B); Percentage of Participants Maintaining a Physician's Global Assessment (PGA) Response During the Double-Blind Treatment Withdrawal (Period B); Percentage of Participants Achieving a PASI75 Response During CP-690,550 Re-Treatment (Period C) Among Those Who Had a Greater Than (>)50% Reduction of Visit A4/Week 24 PASI Response During Double-Blind Treatment Withdrawal (Period B); Percentage of Participants Achieving a PGA Response of Clear...

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov