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RecruitingNCT06830044

Milsaperidone added to medication for major depression

About this titleRead the official source — NCT06830044

This study evaluates the safety and effectiveness of Milsaperidone for people with depression.

Medication studyAges 18–65Multiple countries
The study in practice

Understand this study

What is this study about?

This study evaluates the safety and effectiveness of Milsaperidone for people with depression.

Who could participate?

This study is for people with depression. Listed age limits: 18 years to 65 years. Other eligibility criteria apply.

Listed locations
Phoenix and 52 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateStarted: March 3, 2025
Recruitment status
Recruiting
Enrollment listed in the registry
500
Sponsor
Vanda Pharmaceuticals
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, Bulgaria, Czechia, ...
Age range
From 18 Years to 65 Years
Official registry ID
NCT06830044
Official title
Show the full official title

A Randomized, Double-Blind, Placebo-controlled Multicenter Study to Assess the Efficacy and Safety of Milsaperidone as Adjunctive Therapy in the Treatment of Patients With Major Depressive Disorder

Recruitment & locations

Currently recruiting

Phoenix, United States · Little Rock, United States · Garden Grove, United States

42 more locations
  • Orange, United States
  • Redlands, United States
  • San Jose, United States
  • Walnut Creek, United States
  • Colorado Springs, United States
  • Fort Myers, United States
  • Miami, United States
  • Tampa, United States
  • Snellville, United States
  • Chicago, United States
  • Carmel, United States
  • Boston, United States
  • Saint Charles, United States
  • Las Vegas, United States
  • New York, United States
  • Staten Island, United States
  • Charlotte, United States
  • Cincinnati, United States
  • Media, United States
  • Houston, United States
  • Plano, United States
  • Richardson, United States
  • Witchita Falls, United States
  • Bellevue, United States
  • Kardzhali, Bulgaria
  • Pleven, Bulgaria
  • Plovdiv, Bulgaria
  • Sofia, Bulgaria
  • Targovishte, Bulgaria
  • Varna, Bulgaria
  • Vratsa, Bulgaria
  • Brno, Czechia
  • Pilsen, Czechia
  • Poruba, Czechia
  • Prague, Czechia
  • Bialystok, Poland
  • Bydgoszcz, Poland
  • Gdansk, Poland
  • Katowice, Poland
  • Suchy Las, Poland
  • Torun, Poland
  • Czechia

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FAQ

Questions about this study

What is this study about?

This study evaluates the safety and effectiveness of Milsaperidone for people with depression.

Who is behind this study?

The study sponsor is Vanda Pharmaceuticals.

Does this study involve medication?

Yes. The study involves medication, including Milsaperidone and Placebo.

Who can participate?

This study is for people with depression. Listed age limits: 18 years to 65 years. Other eligibility criteria apply.

Is this study still recruiting?

The registry lists this study as recruiting.

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