Viewing Study NCT03051256


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Study NCT ID: NCT03051256
Status: COMPLETED
Last Update Posted: 2023-11-01
First Post: 2017-02-03
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: Safety, Tolerability, PK Profile, and Symptom Response of a 7-Day Dosing With 25 mg or 50 mg Daily of REL-1017 in MDD
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Study Design

Study Type: INTERVENTIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: None
Target Duration: None
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Bio Spec Retention: None
Bio Spec Description: None
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Phases

Phase Brief Phase Text View
None PHASE2 View
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