Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02472795 · ClinicalTrials.gov registry record · Phase 1

Clinical Study to Investigate the Biological Activity, Safety, Tolerability, and Pharmacokinetics of ACT-334441 in Subjects With Systemic Lupus Erythematosus

A Phase 1 study, sponsored by Viatris Innovation.

Completed
Registry status
Phase 1
Development phase
105
Enrollment target

NCT02472795: Completed Phase 1 study, sponsored by Viatris Innovation.

NCT02472795 is a Phase 1 study that has completed, run by Viatris Innovation. The registered enrollment target is 105 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (75% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02472795, a Phase 1 study, has completed, sponsored by Viatris Innovation.

COMPLETED
Registry status
Phase 1
Development phase
105 participants
Enrollment target

Study Summary

International trial to evaluate the biological activity and safety of cenerimod (ACT-334441) in systemic lupus erythematosus (SLE) patients.

Primary Outcome

The primary objective of the clinical study was to asses whether cenerimod could reduce the number of circulating lymphocytes in the bloodstream of people with systemic lupus erythematosus (SLE). The change was defined as: Total lymphocyte count at end-of-treatment (EOT) minus total lymphocyte count at baseline. A negative change over time indicates that the number of peripheral circulating lymphocytes has decreased. The reduction of the total lymphocyte count over a treatment period indicate

Interventions

  • DRUG Matching placebo
  • DRUG Cenerimod

Trial Details

FieldValue
Enrollment Target 105 participants
Start Date 2015-06-01
Est. Completion 2017-02-28
Phase Phase 1
Viatris Innovation

11 total trials

What the finished NCT02472795 record still lists

NCT02472795 is an interventional study that assigns participants to a tested intervention. The registered 105 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (75% higher).

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

NCT02472795 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02472795 about?

NCT02472795 is a clinical study titled "Clinical Study to Investigate the Biological Activity, Safety, Tolerability, and Pharmacokinetics of ACT-334441 in Subjects With Systemic Lupus Erythematosus". International trial to evaluate the biological activity and safety of cenerimod (ACT-334441) in systemic lupus erythematosus (SLE) patients.

What is the current status of trial NCT02472795?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 105 participants. The study started on 2015-06-01. Estimated completion is 2017-02-28.

What interventions are being tested in trial NCT02472795?

The interventions under investigation include: Matching placebo (DRUG), Cenerimod (DRUG).

Who is sponsoring clinical trial NCT02472795?

This trial is sponsored by Viatris Innovation, which has 11 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02472795's enrollment target sits among peer trials

105 533rd of 2000 higher than 1,465 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03372317 · 105 participants

    Tau PET in Imaging and Cognition: Healthy Adults From 55-90

  • NCT04253964 · 105 participants · Phase 2

    Pilot Study of Performance Status 2 vs. Performance Status 0-1 Non-small Cell Lung Cancer Patients Treated With Chemo/Immunotherapy

  • NCT04742452 · 105 participants · NA

    Comparison of Partial Rotator Cuff Repair vs. Superior Capsular Reconstruction for Irreparable Rotator Cuff Tears

  • NCT04875429 · 105 participants · NA

    Zenith® Fenestrated+ Clinical Study

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT02472795, the US trial registry maintained by the National Library of Medicine. NCT02472795 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.