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Last Updated: October 31, 2024

CLINICAL TRIALS PROFILE FOR SAGE-718


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Clinical Trials for SAGE-718

Trial ID Title Status Sponsor Phase Summary
NCT03770780 ↗ A Study to Assess the Electrophysiology, Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Response Using Magnetic Resonance Imaging of SAGE-718 Using a Ketamine Challenge in Healthy Subjects Completed Sage Therapeutics Phase 1 This study is a phase 1, double-blind, placebo-controlled crossover study of SAGE-718 using a ketamine challenge, to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamic response using magnetic resonance imaging in healthy subjects
NCT03771586 ↗ A Study to Assess the Electrophysiology, Safety, Tolerability, and Pharmacokinetics of SAGE-718 Using a Ketamine Challenge in Healthy Subjects Completed Sage Therapeutics Phase 1 This study is a phase 1, double-blind, placebo-controlled crossover study of single, oral dose of SAGE-718 using a ketamine challenge, to evaluate the electrophysiology, safety, tolerability, and pharmacokinetics in healthy subjects
NCT03787758 ↗ A Study to Evaluate Safety, Tolerability, and Pharmacokinetics of SAGE-718 Oral Solution in Patients With Huntington's Disease - Part B Completed Sage Therapeutics Phase 1 This study is a phase 1, double-blind, placebo-controlled, multiple ascending dose study to determine the safety, tolerability, and pharmacokinetics of SAGE-718 oral solution in healthy adults (Part A) with an open-label cohort of patients with Huntington's disease (Part B)
NCT03844906 ↗ A Study to Assess Electrophysiology, Safety, Tolerability, and Pharmacokinetics of Multiple Doses of SAGE-718 Using Ketamine Challenge in Healthy Subjects Completed Sage Therapeutics Phase 1 This study is a Phase 1, randomized, double-blind, placebo-controlled study of multiple doses of SAGE-718 using ketamine challenge to evaluate the electrophysiology, safety, tolerability, and pharmacokinetics in healthy subjects.
NCT04476017 ↗ A Study to Evaluate the Safety and Tolerability of SAGE-718 in Participants With Parkinson's Disease Mild Cognitive Impairment (PD-MCI) Recruiting Sage Therapeutics Phase 2 The primary purpose of this two-part study is to evaluate the safety and tolerability of SAGE-718 and its effects on cognitive, neuropsychiatric, and motor symptoms in participants with PD-MCI.
NCT04602624 ↗ A Study to Evaluate the Safety and Tolerability of SAGE-718 in Participants With Mild Cognitive Impairment or Mild Dementia Due to Alzheimer's Disease (AD) Completed Sage Therapeutics Phase 2 The primary purpose of this study is to evaluate the safety and tolerability of SAGE-718 and its effects on cognitive and neuropsychiatric symptoms in participants with mild cognitive impairment (MCI) or mild dementia due to Alzheimer's disease (AD).
NCT05107128 ↗ A Study to Evaluate the Effect of SAGE-718 on Cognitive Function in Participants With Huntington's Disease (HD) Not yet recruiting Sage Therapeutics Phase 2 The primary purpose of this study is to evaluate the effect of SAGE-718 on cognitive performance and functioning in participants with HD.
>Trial ID >Title >Status >Phase >Summary

Clinical Trial Conditions for SAGE-718

Condition Name

Condition Name
Intervention Trials
Healthy Volunteer 3
Huntington Disease 3
Cognitive Dysfunction 3
Mild Dementia 2
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Condition MeSH

Condition MeSH
Intervention Trials
Cognitive Dysfunction 4
Huntington Disease 4
Dementia 2
Alzheimer Disease 2
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Clinical Trial Locations for SAGE-718

Trials by Country

Trials by Country
Location Trials
United States 24
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Trials by US State

Trials by US State
Location Trials
California 6
New Jersey 4
Nebraska 2
Maryland 2
Georgia 2
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Clinical Trial Progress for SAGE-718

Clinical Trial Phase

Clinical Trial Phase
Clinical Trial Phase Trials
Phase 3 1
Phase 2 6
Phase 1 4
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Clinical Trial Status

Clinical Trial Status
Clinical Trial Phase Trials
Not yet recruiting 5
Completed 5
Recruiting 1
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Clinical Trial Sponsors for SAGE-718

Sponsor Name

Sponsor Name
Sponsor Trials
Sage Therapeutics 11
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Sponsor Type

Sponsor Type
Sponsor Trials
Industry 11
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