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NCT01265667 · ClinicalTrials.gov registry record · Phase 2

Trial of CF101 to Treat Patients With Psoriasis

A Phase 2 study, sponsored by Can-Fite BioPharma.

Completed
Registry status
Phase 2
Development phase
293
Enrollment target

NCT01265667: Completed Phase 2 study, sponsored by Can-Fite BioPharma.

NCT01265667 is a Phase 2 study that has completed, run by Can-Fite BioPharma. The registered enrollment target is 293 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (120% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01265667, a Phase 2 study, has completed, sponsored by Can-Fite BioPharma.

COMPLETED
Registry status
Phase 2
Development phase
293 participants
Enrollment target

Study Summary

Eligible patients with Psoriasis will be treated with CF101 or placebo twice daily for 16 weeks. All subjects will receive open-lable CF101 in weeks 17-32.

Primary Outcome

Achievement of PASI 75 indicates a 75% reduction in the PASI score, which ranges from 0 (no disease) to 72 (maximal disease)

Interventions

  • DRUG Placebo
  • DRUG CF101

Trial Details

FieldValue
Enrollment Target 293 participants
Start Date 2011-07
Est. Completion 2015-05
Phase Phase 2
Can-Fite BioPharma

4 total trials

What the finished NCT01265667 record still lists

NCT01265667 is an interventional study that assigns participants to a tested intervention. The registered 293 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 (120% higher).

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

NCT01265667 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01265667 about?

NCT01265667 is a clinical study titled "Trial of CF101 to Treat Patients With Psoriasis". Eligible patients with Psoriasis will be treated with CF101 or placebo twice daily for 16 weeks. All subjects will receive open-lable CF101 in weeks 17-32.

What is the current status of trial NCT01265667?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 293 participants. The study started on 2011-07. Estimated completion is 2015-05.

What interventions are being tested in trial NCT01265667?

The interventions under investigation include: Placebo (DRUG), CF101 (DRUG).

Who is sponsoring clinical trial NCT01265667?

This trial is sponsored by Can-Fite BioPharma, which has 4 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01265667's enrollment target sits among peer trials

293 191st of 2000 higher than 1,810 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 NCT01265667, the US trial registry maintained by the National Library of Medicine. NCT01265667 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.