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

NCT01491529 · ClinicalTrials.gov registry record · Phase 2

Evaluation of the Efficacy and Safety of Modified Release AFQ056 in Parkinson's Patients With L-dopa Induced Dyskinesias

A Phase 2 study, sponsored by Novartis Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
154
Enrollment target

NCT01491529: Completed Phase 2 study, sponsored by Novartis Pharmaceuticals.

NCT01491529 is a Phase 2 study that has completed, run by Novartis Pharmaceuticals. The registered enrollment target is 154 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (16% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01491529, a Phase 2 study, has completed, sponsored by Novartis Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
154 participants
Enrollment target

Study Summary

This study will assess the efficacy and safety of modified release AFQ056 in patients that have Parkinson's Disease L-dopa Induced Dyskinesias (PD-LID)

Primary Outcome

The modified AIMS is a scale used to assess dyskinesia. It focuses on six different parts of the body and rates abnormal movements from 0 (absence of dyskinesia to 4 (severe) (maximal score, 24). Change from baseline to Week 12 will be analyzed using the mixed effect repeated measures model (MMRM) including treatment, pooled center, week, treatment by week interaction as fixed effects and baseline total score as covariate with an unstructured covariance structure.

Interventions

  • DRUG Placebo
  • DRUG AFQ056

Trial Details

FieldValue
Enrollment Target 154 participants
Start Date 2012-04
Est. Completion 2013-04
Phase Phase 2
Novartis Pharmaceuticals

1,375 total trials

What the finished NCT01491529 record still lists

NCT01491529 is an interventional study that assigns participants to a tested intervention. The registered 154 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 (16% higher).

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

NCT01491529 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01491529 about?

NCT01491529 is a clinical study titled "Evaluation of the Efficacy and Safety of Modified Release AFQ056 in Parkinson's Patients With L-dopa Induced Dyskinesias". This study will assess the efficacy and safety of modified release AFQ056 in patients that have Parkinson's Disease L-dopa Induced Dyskinesias (PD-LID)

What is the current status of trial NCT01491529?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 154 participants. The study started on 2012-04. Estimated completion is 2013-04.

What interventions are being tested in trial NCT01491529?

The interventions under investigation include: Placebo (DRUG), AFQ056 (DRUG).

Who is sponsoring clinical trial NCT01491529?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01491529's enrollment target sits among peer trials

154 448th of 2000 higher than 1,552 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

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

  • NCT04300998 · 154 participants

    Study of CAR-T Therapy in Older Patients

  • NCT04597372 · 154 participants · Phase 2

    Impact of Tamsulosin on Post-Operative Urinary Retention Following Pelvic Reconstructive Surgery

  • NCT05294042 · 154 participants · NA

    Patient Navigators for Children's Community Mental Health Services in High Poverty Urban Communities

  • NCT05512390 · 154 participants · Phase 1

    A Study to Assess the Adverse Events, Change in Disease Activity, and How Intravenously Infused ABBV-319 Moves Through the Bodies of Adult Participants With Relapsed or Refractory (R/R) Diffuse Large B-cell Lymphoma (DLBCL), Follicular Lymphoma (FL), or Chronic Lymphocytic Leukemia (CLL)

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01491529, the US trial registry maintained by the National Library of Medicine. NCT01491529 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.