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CSR Summary
Not Yet Available
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NCT03434041
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Primary Citation
Not Yet Available
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Data Specification
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Trial Information
Generic NameEsketamineProduct NameSPRAVATO®Therapeutic AreaNervous SystemProduct ClassPsychoanalepticsPharmacological SubgroupAntidepressantsChemical SubgroupOther AntidepressantsCondition StudiedDepressive Disorder, Treatment-Resistant
Sponsor Protocol NumberESKETINTRD3006Enrollment252Data PartnerJohnson & Johnson% FemaleN/AMean/Median Age (Years)37.3% WhiteN/A
Supporting Documentation
- Collected Datasets Available
- Protocol with Amendments Available
- Statistical Analysis Plan Available
- Clinical Study Report Available
Approved Data Requests Associated with this Trial
- 2025-0756 : Multi-Analyst Reanalysis of IPD on Esketamine and Suicidality (Team Three)
- 2025-0752 : Multi-Analyst Reanalysis of IPD on Esketamine and Suicidality (Team Two)
- 2025-0748 : Multi-Analyst Reanalysis of IPD on Esketamine and Suicidality (Team One)
- 2025-0544 : Placebo Response Magnitude and Associated Factors in Randomized Double-Blind Trials of Ketamine for Depression
- 2025-0352 : ALL-EMBRACED: clinicAL triaLs web-sErvice to Modify eligiBility cRiteria and pre-screening viA artifiCial intElligence methoDs
- 2025-0004 : Differential Effects of Esketamine on Individual Symptoms of Major Depression
- 2024-0612 : Effects of ketamine and esketamine on death, suicidal behavior and suicidal ideation in psychiatric disorders: A systematic review and meta-analysis
