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CompletedNCT07193901

A Study to Evaluate the Efficacy, Safety, and Pharmacokinetic Characteristics of (R)-Ketamine Hydrochloride Nasal Spray in Patients With Depression and Acute Suicide prevention or Behavior

Medication studyAges 18–64China
The study in practice

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Who was this study for?

This study was for people with depression. Listed age limits: 18 years to 64 years. Other eligibility criteria applied.

Listed locations
Beijin and 14 more locationsSee all locations and recruitment
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.

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Study clarity

Study information

Study start dateStarted: May 27, 2025
Recruitment status
Completed
Enrollment listed in the registry
98
Sponsor
Sichuan Purity Pharmaceutical Technology Co., Ltd.
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
China
Age range
From 18 Years to 64 Years
Official registry ID
NCT07193901
Official title
Show the full official title

A Randomized, Double-blind, Placebo-controlled Phase Il Study to Evaluate the Efficacy, Safety, and Pharmacokinetic Characteristics of (R)-Ketamine Hydrochloride Nasal Spray in Patients With Depression and Acute Suicidal Ideation or Behavior

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Recruitment & locations

Completed

Beijin · Beijing · Changsha

9 more locations
  • Chengdu
  • Hangzhou
  • Hefei
  • Luzhou
  • Nanchang
  • Ningbo
  • Suzhou
  • Wuxi
  • Zhumadian

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Sichuan Purity Pharmaceutical Technology Co., Ltd., a pharmaceutical company.

Did this study involve medication?

Yes. The study involved medication, including Low Dose PRT042 nasal spray, median Dose PRT042 nasal spray, high dose PRT042 nasal spray and placebo.

Who was this study for?

This study was for people with depression. Listed age limits: 18 years to 64 years. Other eligibility criteria applied.

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