HopeStage
Back to all studies
CompletedNCT06510504

Efficacy of BNC210 in Acute, As-needed Treatment of Anxiety in Social Anxiety Disorder - 1

Researchers compared 225 mg BNC210 and placebo, tracking side effects to assess safety in adults with an anxiety condition.

Medication studyAges 18–65United States
The study in practice

Understand this study

What did researchers investigate?

Researchers compared 225 mg BNC210 and placebo, tracking side effects to assess safety in adults with an anxiety condition.

Who was this study for?

This study was for people with anxiety. Listed age limits: 18 years to 65 years. Other eligibility criteria applied.

Listed locations
Encino, United States · La Jolla, United States and 18 more locationsSee all locations and recruitment
Activities
Medication described in the protocol · Placebo comparator
Compensation
Payment and expense reimbursement have not been verified.
Study clarity

Study information

Study start dateStarted: August 6, 2024
Recruitment status
Completed
Enrollment listed in the registry
370
Sponsor
Bionomics Limited
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States
Age range
From 18 Years to 65 Years
Official registry ID
NCT06510504
Official title
Show the full official title

A Phase 3, Randomized, Double-blind, 2-arm, Parallel-group, Placebo-controlled Study to Evaluate the Efficacy and Safety of BNC210 for the Acute, As-needed Treatment of Anxiety in Adults With Social Anxiety Disorder

Looking for a study you can join?

Explore recruiting studies

Recruitment & locations

Completed

Encino · La Jolla · Los Angeles

17 more locations
  • Oceanside
  • San Diego
  • San Jose
  • Sherman Oaks
  • Temecula
  • Jacksonville
  • Lauderhill
  • Miami Lakes
  • Orlando
  • Tampa
  • Decatur
  • Boston
  • Princeton
  • Brooklyn
  • Charlotte
  • Media
  • Austin
FAQ

Questions about this study

What did researchers investigate?

Researchers compared 225 mg BNC210 and placebo, tracking side effects to assess safety in adults with an anxiety condition.

Who is behind this study?

The study sponsor is Bionomics Limited.

Did this study involve medication?

Yes. The study involved medication, including 225 mg BNC210 and Placebo.

Who was this study for?

This study was for people with anxiety. Listed age limits: 18 years to 65 years. Other eligibility criteria applied.

Explore other studies

Want to find a study that may fit you better?

Answer a few simple questions to explore HopeStage studies by condition, country, and situation.

Find a study that may fit me