KarXT for Bipolar Disorder
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests the effectiveness and safety of a new treatment, KarXT, for managing mania in people with Bipolar-I Disorder. Participants will receive either KarXT or a placebo (a substance with no therapeutic effect) alongside their regular medication, such as lithium, valproate, or lamotrigine. It targets individuals currently experiencing a severe manic episode that requires hospitalization and are on a stable dose of specific mood stabilizers. As a Phase 3 trial, this is the final step before FDA approval, offering participants a chance to contribute to a potentially groundbreaking treatment.
Do I have to stop taking my current medications for the trial?
The trial requires that you stay on a stable dose of lithium, valproate, or lamotrigine for at least two weeks before screening. If you're on valproate, you must have been taking it for at least seven months.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that KarXT was tested for safety in earlier studies. Most side effects were mild and occurred in the first one to two weeks of treatment, resolving quickly. Overall, participants generally tolerated the treatment well. This suggests that KarXT is likely safe for people, though individual experiences may vary.12345
Why do researchers think this study treatment might be promising for bipolar disorder?
Unlike standard treatments for bipolar disorder, which often rely on mood stabilizers like lithium, valproate, or lamotrigine, KarXT offers a new approach. Researchers are excited about KarXT because it combines xanomeline, a muscarinic receptor agonist, with trospium chloride, which reduces unwanted side effects. This unique mechanism targets both the M1 and M4 muscarinic receptors in the brain, potentially improving cognition and mood symptoms more effectively than current options. By offering a novel pathway for managing bipolar disorder, KarXT could provide a significant advancement in treatment.
What evidence suggests that KarXT might be an effective treatment for mania in Bipolar-I Disorder?
Research has shown that KarXT yields promising results for mental health conditions. In one study involving individuals with schizophrenia, KarXT significantly improved symptoms over a year. Another study found that a patient using KarXT for just five weeks experienced a 39.53% reduction in symptom severity. These findings suggest that KarXT might also help reduce symptoms in bipolar disorder. In this trial, participants will receive either KarXT combined with Lithium, Valproate, or Lamotrigine, or a placebo combined with these medications. While specific data for bipolar disorder is still being gathered, the positive results in related conditions are encouraging.678910
Who Is on the Research Team?
Bristol-Myers Squibb
Principal Investigator
Bristol-Myers Squibb
Are You a Good Fit for This Trial?
This trial is for adults with Bipolar-I disorder experiencing a manic episode, who are hospitalized and have been on a stable dose of lithium, valproate, or lamotrigine for at least two weeks. They must have a BMI between 18-40 kg/m2 and meet specific severity criteria. Excluded are those with certain liver diseases, other primary psychiatric disorders within the last year, recent substance abuse issues, suicidal risk behaviors, or conditions like irritable bowel syndrome.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive adjunctive KarXT or placebo alongside Lithium, Valproate, or Lamotrigine for the treatment of mania
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- KarXT
Find a Clinic Near You
Who Is Running the Clinical Trial?
Bristol-Myers Squibb
Lead Sponsor
Christopher Boerner
Bristol-Myers Squibb
Chief Executive Officer since 2023
PhD in Business Administration from the Haas School of Business, University of California, Berkeley; BA in Economics and History from Washington University in St. Louis
Deepak L. Bhatt
Bristol-Myers Squibb
Chief Medical Officer since 2024
MD from Yale University; MSc in Clinical Epidemiology from the University of Pennsylvania