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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04855747
Other study ID # REL-1017-302
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date March 30, 2021
Est. completion date June 2024

Study information

Verified date February 2024
Source Relmada Therapeutics, Inc.
Contact Medical Director
Phone 786-638-7384
Email clinicaltrials@relmada.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is an outpatient, 2-arm, Phase 3, multicenter, randomized, double-blind, placebo-controlled study to assess the efficacy and safety of REL-1017 once daily (QD) as an adjunctive treatment of Major Depressive Disorder. Study participants will continue to take their current antidepressant therapy in addition to the study drug or placebo for the duration of the treatment period.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date June 2024
Est. primary completion date June 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Adults 18 to 65 years, inclusive. - Diagnosed with Major Depressive Disorder (MDD) based on Structured Clinical Interview for DSM-5 (SCID-5) for MDD. - Current major depressive episode. - Treated on approved, stable first-line anti-depressant therapy with inadequate response to 1 to 3 valid courses of treatment with an antidepressant medication Exclusion Criteria: - Any current and primary psychiatric disorder other than Major Depressive Disorder. - Severe alcohol or substance use disorder. - History of bipolar I and II disorder, psychosis, and/or mania. - Acute or chronic condition that, in the Investigator's opinion, would limit the subject's ability to complete or participate in this clinical study. - Any lifetime experience of having received ketamine or esketamine as a treatment for MDD, or as part of a clinical trial.

Study Design


Intervention

Drug:
REL-1017
REL-1017 tablet
Placebo
Placebo tablet

Locations

Country Name City State
United States Relmada Site Allentown Pennsylvania
United States Relmada Site Austin Texas
United States Relmada Site Austin Texas
United States Relmada Site Baltimore Maryland
United States Relmada Site Baytown Texas
United States Relmada Site Beachwood Ohio
United States Relmada Site Bellaire Texas
United States Relmada Site Bellevue Washington
United States Relmada Site Bellflower California
United States Relmada Site Boise Idaho
United States Relmada Site Boston Massachusetts
United States Relmada Site Boston Massachusetts
United States Relmada Site Bryant Arkansas
United States Relmada Site Cedarhurst New York
United States Relmada Site Chicago Illinois
United States Relmada Site Chicago Illinois
United States Relmada Site Cincinnati Ohio
United States Relmada Site Cincinnati Ohio
United States Relmada Site Culver City California
United States Relmada Site Dallas Texas
United States Relmada Site Denver Colorado
United States Relmada Site Draper Utah
United States Relmada Site Encino California
United States Relmada Site Everett Washington
United States Relmada Site Friendswood Texas
United States Relmada Gaithersburg Maryland
United States Relmada Site Gaithersburg Maryland
United States Relmada Site Glendale California
United States Relmada Site Hallandale Beach Florida
United States Relmada Site Hialeah Florida
United States Relmada Site Houston Texas
United States Relmada Site Houston Texas
United States Relmada Site Imperial California
United States Relmada Site Jacksonville Florida
United States Relmada Site La Jolla California
United States Relmada Site Lafayette California
United States Relmada Site Lake City Florida
United States Relmada Site Lakeland Florida
United States Relmada Site Las Vegas Nevada
United States Relmada Site Memphis Tennessee
United States Relmada Site Miami Florida
United States Relmada Site Miami Florida
United States Relmada Site Miami Florida
United States Relmada Site Miami Florida
United States Relmada Site Miami Springs Florida
United States Relmada Site Middleburg Heights Ohio
United States Relmada Site New York New York
United States Relmada Site Newport Beach California
United States Relmada Site Norwich Connecticut
United States Relmada Site O'Fallon Missouri
United States Relmada Site Okeechobee Florida
United States Relmada Site Orange California
United States Relmada Site Orange City Florida
United States Relmada Site Overland Park Kansas
United States Relmada Site Phoenix Arizona
United States Relmada Site Phoenix Arizona
United States Relmada Site Plano Texas
United States Relmada Site Princeton New Jersey
United States Relmada Site Redlands California
United States Relmada Site San Diego California
United States Relmada Site Saraland Alabama
United States Relmada Site Savannah Georgia
United States Relmada Site Stanford California
United States Relmada Site Staten Island New York
United States Relmada Site Tampa Florida
United States Relmada Site Tampa Florida
United States Relmada Site Tampa Florida
United States Relmada Site Temecula California
United States Relmada Site Toms River New Jersey
United States Relmada Site Torrance California
United States Relmada Site Upland California
United States Relmada Site Watertown Massachusetts
United States Relmada Site Waukesha Wisconsin
United States Relmada Site Weldon Spring Missouri
United States Relmada Site West Chester Ohio
United States Relmada Site West Palm Beach Florida
United States Relmada Site Wichita Falls Texas
United States Relmada Site Winter Park Florida

Sponsors (1)

Lead Sponsor Collaborator
Relmada Therapeutics, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in the MADRS10 total score Therapeutic efficacy of REL-1017 as adjunctive treatment versus placebo in the Montgomery-Asberg Depression Rating Scale (MADRS10) A higher MADRS score indicates more severe depression, and each item yields a score of 0 to 6. The overall score ranges from Oto 60 with scores above 34 indicating severe depression.
A negative change from baseline indicates improvement.
Day 28
Secondary Change in CGI-S score Therapeutic efficacy of REL-1017 as an adjunctive treatment versus placebo in Clinical Global Impression of Severity (CGI-S) The CGI-S is a standard method used in clinical studies to quantify and track patient progress and treatment response over time. The scale is composed of 7 ratings: 1 = normal, not at all ill; 2 = borderline ill; 3 = mildly ill; 4 = moderately ill; 5 = markedly ill; 6 = severely ill; and 7 = among the most extremely ill patients.
The score ranges from 1 to 7, and a lower CGI-S score indicates lower levels of depression.
Day 28
Secondary Change in the MADRS10 total score Therapeutic efficacy of REL-1017 as adjunctive treatment versus placebo in the Montgomery-Asberg Depression Rating Scale (MADRS10) A higher MADRS score indicates more severe depression, and each item yields a score of 0 to 6. The overall score ranges from Oto 60 with scores above 34 indicating severe depression.
A negative change from baseline indicates improvement.
Day 7
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