Patient Guide: A Study to Evaluate the Efficacy and Safety of Adjunctive KarXT for the Treatment of Mania, With or Without Mixed Features, in Participants With Bipolar-I Disorder Taking Lithium, Valproate, or Lamotrigine

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 66 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT07140913
Status: 🟢 Enrolling Now
Condition: Mania, Bipolar Disorder
Phase: PHASE3

Where You Can Participate

This study is available at 66 locations across the country.

Top locations include:
  • • Bentonville, Arkansas
  • • Little Rock, Arkansas
  • • Chino, California
  • • And 63 more locations

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A Study to Evaluate the Efficacy and Safety of Adjunctive KarXT for the Treatment of Mania, With or Without Mixed Features, in Participants With Bipolar-I Disorder Taking Lithium, Valproate, or Lamotrigine - Join Clinical Trial NCTNCT07140913

How to Join This Clinical Trial - NCTNCT07140913

Learn how to participate in this PHASE3 trial studying an investigational therapy for Mania, Bipolar Disorder. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Mania, Bipolar Disorder. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Mania, Bipolar Disorder
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT07140913 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 66 locations. Find a study site near you:

Clinical Research Site

Bentonville, Arkansas 72712 - United States

Status: RECRUITING

Clinical Research Site

Little Rock, Arkansas 72204 - United States

Status: RECRUITING

Clinical Research Site

Chino, California 91710 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Costa Mesa, California 92626 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Culver City, California 90230 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

La Habra, California 90631-3842 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Montclair, California 91763 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Orange, California 92868 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Riverside, California 92506 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Hallandale, Florida 33009 - United States

Status: NOT_YET_RECRUITING

And 56 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Mania, Bipolar Disorder:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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