This is a Phase 1b/2a clinical trial to evaluate the safety, tolerability, and efficacy of RLS103 (cannabidiol [CBD] inhaled dry powder) to relieve the anxiety induced by a public speaking challenge in adults with social anxiety disorder (SAD).
Subject participation will last 4 - 6 weeks. Upon signing an informed consent, all subjects will enter a screening phase lasting up to 3 weeks and including history, physical examination, laboratory tests, ECG, spirometry, and psychological tests. Subjects will undergo a public speaking test after screening tests are performed and eligibility is confirmed. One week after the completion of the public speaking test, subjects will come back for a follow-up visit that will involve a repeat of the safety and psychiatric assessments conducted during screening.
| Condition | Social Anxiety Disorder |
|---|---|
| Treatment | Low dose RLS103, High dose RLS103, placebo inhaled dry powder |
| Clinical Study Identifier | NCT05429788 |
| Sponsor | Receptor Life Sciences |
| Last Modified on | 29 March 2023 |
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