Bonita Springs, FLNCT07365462Now EnrollingIRB Ready

Tardive Dyskinesia Clinical Trial in Bonita Springs, FL

Access cutting-edge tardive dyskinesia treatment through this clinical trial at a research site in Bonita Springs. Study-provided care at no cost to qualified participants.

Sponsored by Neurocrine Biosciences

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Expert Care in Bonita Springs

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IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related tardive dyskinesia treatment provided free

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Check if you qualify for this tardive dyskinesia clinical trial in Bonita Springs, FL

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Why Participate?

  • No-Cost Study Care

  • Local to Bonita Springs

    Convenient for FL residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Bonita Springs site if eligible
  4. 4Begin participation

About This Tardive Dyskinesia Study in Bonita Springs

The primary objective of this study is to evaluate the efficacy of NBI-1065890 compared with placebo for the treatment of tardive dyskinesia (TD) in adult participants.

Sponsor: Neurocrine Biosciences

Who Can Participate

Inclusion Criteria

Medically confirmed diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder, or major depressive disorder (MDD) as defined in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) for at least 3 months prior to screening.
Medically confirmed diagnosis of neuroleptic-induced TD as defined in the DSM-5 for at least 3 months prior to screening.
Moderate or severe TD (AIMS Item 8, severity of abnormal movement overall) as assessed by a blinded, external AIMS video reviewer using a video recording of the participant's AIMS assessment administered at the clinical site by a blinded, certified site AIMS rater. The AIMS dyskinesia total score (sum of Items 1 to 7) must be ≥6 as assessed by the blinded, external AIMS video reviewer. Key

Exclusion Criteria

Comorbid parkinsonism (drug-induced or otherwise) or more than a minimal level of extrapyramidal signs/symptoms, as documented by a score on the Modified Simpson-Angus Scale (mSAS) (excluding Items 8 and 10) \>6 at screening or Day -1 (baseline) or a score \>3 in any one item (excluding Items 8 and 10).
Barnes Akathisia Rating Scale (BARS) global clinical assessment score ≥2 at screening or Day -1.
Brief Psychiatric Rating Scale (BPRS) total score ≥50 at screening or Day -1.
Hospitalized for schizophrenia, schizoaffective disorder, bipolar disorder, or MDD within 6 months of screening.
Participant has an unstable medical condition or unstable chronic disease.
Any known history of neuroleptic malignant syndrome (NMS). Note: Other protocol-defined inclusion and exclusion criteria may apply.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Bonita Springs?

Yes, this clinical trial (NCT07365462) has an active research site in Bonita Springs, FL that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Tardive Dyskinesia Treatment Options in Bonita Springs, FL

If you're searching for tardive dyskinesia treatment options in Bonita Springs, FL, this clinical trial (NCT07365462) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Bonita Springs research site is actively enrolling participants for this clinical trial. You'll receive care from experienced tardive dyskinesia specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all tardive dyskinesia clinical trials near you to find additional studies recruiting in your area.

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