Clin2
NCT07799493Possibly a fitRecruiting

Studying caplyta for adults with social anxiety disorder

Social Anxiety Disorder (SAD)

Treatments studied

Part of Mental health clinical trials.

This study tests whether the medication caplyta (lumateperone) helps reduce symptoms of social anxiety disorder compared to a placebo. If it works, it could give people a new treatment option.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 4
Enrollment
40 people
Ages
18 years to 65 years
Study type
Interventional

Who can take part

  • You are between 18 and 65 years old.
  • You have been diagnosed with social anxiety disorder.
  • Your social anxiety symptoms are at least moderately severe.
  • You do not have certain other mental health conditions like schizophrenia or bipolar disorder.
  • You are not at immediate risk of suicide.
  • You are not currently taking certain other psychiatric medications.
  • If you could become pregnant, you agree to use birth control during the study and for 4 weeks after.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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