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NCT02106195 · ClinicalTrials.gov registry record · Phase 2

A Safety and Tolerability Study of Belumosudil (KD025) Treatment in Subjects With Moderately Severe Psoriasis Vulgaris

A Phase 2 study, sponsored by Kadmon Corporation.

Completed
Registry status
Phase 2
Development phase
8
Enrollment target

NCT02106195: Completed Phase 2 study, sponsored by Kadmon Corporation.

NCT02106195 is a Phase 2 study that has completed, run by Kadmon Corporation. The registered enrollment target is 8 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02106195, a Phase 2 study, has completed, sponsored by Kadmon Corporation.

COMPLETED
Registry status
Phase 2
Development phase
8 participants
Enrollment target

Study Summary

The primary objective is to assess the safety and tolerability of 200 mg of belumosudil administered orally once daily for 28 days.

Primary Outcome

To evaluate the safety and tolerability of 200 mg of belumosudil administered PO QD to subjects for treatment of psoriasis

Interventions

  • DRUG Belumosudil

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2014-04
Est. Completion 2014-09
Phase Phase 2
Kadmon Corporation

15 total trials

What the finished NCT02106195 record still lists

NCT02106195 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (94% lower).

The record links to 0 conditions, and to 1 intervention - of which Belumosudil is the first listed.

NCT02106195 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02106195 about?

NCT02106195 is a clinical study titled "A Safety and Tolerability Study of Belumosudil (KD025) Treatment in Subjects With Moderately Severe Psoriasis Vulgaris". The primary objective is to assess the safety and tolerability of 200 mg of belumosudil administered orally once daily for 28 days.

What is the current status of trial NCT02106195?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 8 participants. The study started on 2014-04. Estimated completion is 2014-09.

What interventions are being tested in trial NCT02106195?

The interventions under investigation include: Belumosudil (DRUG).

Who is sponsoring clinical trial NCT02106195?

This trial is sponsored by Kadmon Corporation, which has 15 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02106195's enrollment target sits among peer trials

8 1990th of 2000 higher than 5 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 NCT02106195, the US trial registry maintained by the National Library of Medicine. NCT02106195 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.