A Study of the Efficacy and Safety of SP-624 in the Treatment of Adults With Major Depressive Disorder

Last updated: April 18, 2025
Sponsor: Sirtsei Pharmaceuticals, Inc.
Overall Status: Active - Recruiting

Phase

2

Condition

Depression

Affective Disorders

Depression (Adult And Geriatric)

Treatment

SP-624

Placebo

Clinical Study ID

NCT06254612
SP-624-202
  • Ages 18-65
  • All Genders

Study Summary

This is a Phase 2B clinical study evaluating the effectiveness and safety of SP-624 as compared to placebo in the treatment of adults with Major Depressive Disorder.

Eligibility Criteria

Inclusion

Key Inclusion Criteria:

  • Males and females, aged 18 to 65 years, inclusive.

  • Meet DSM-5 criteria for moderate to severe MDD, as confirmed by the MiniInternational Neuropsychiatric Interview (MINI).

  • In generally good physical health, in the opinion of the Investigator.

  • Body mass index (BMI) must be ≥ 18 and ≤ 45 kg/m2.

Exclusion

Key Exclusion Criteria:

  • Female who is pregnant, breastfeeding, or less than 6 months postpartum at screen.

  • A history of or current DSM-5 diagnosis of MDD with psychotic features, anyschizophrenia spectrum and other psychotic disorders, bipolar disorder, orpersonality disorder.

  • Presence or history of any known clinically significant cardiovascular disordersincluding, but not limited to: coronary artery disease, heart failure, valvularheart disease, cardiomyopathies, myocardial infarction, chamber enlargement orhypertrophy, or orthostatic hypotension.

  • Presence of uncontrolled hypertension, defined as consistent sitting systolic bloodpressure (SBP) >160 mmHg or consistent sitting diastolic blood pressure (DBP) >95mmHg despite present therapy.

  • Screening laboratory value(s) outside the laboratory reference range that areconsidered to be clinically significant by the Investigator (clinical chemistry,hematology, thyroid function, and urinalysis).

Study Design

Total Participants: 456
Treatment Group(s): 2
Primary Treatment: SP-624
Phase: 2
Study Start date:
March 25, 2024
Estimated Completion Date:
November 30, 2025

Connect with a study center

  • IMA Clinical Research

    Phoenix, Arizona 85012
    United States

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  • SanRo Clinical Research Group

    Bryant, Arkansas 72022
    United States

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    Bellflower, California 90706
    United States

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  • Sun Valley Research Center

    Imperial, California 92251
    United States

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  • Sunwise Clinical Research

    Lafayette, California 94549
    United States

    Active - Recruiting

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    Lemon Grove, California 91945
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    Oceanside, California 92056
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    Colorado Springs, Colorado 80910
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    Jacksonville, Florida 32256
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    Lakeland, Florida 33803
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    Lauderhill, Florida 33319
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    Miami Lakes, Florida 33016
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    Orlando, Florida 32801
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    Pinellas Park, Florida 33782
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    Atlanta, Georgia 30328
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    Meridian, Idaho 83642
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    Elgin, Illinois 60123
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    Boston, Massachusetts 02131
    United States

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    Lincoln, Nebraska 68526
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    Las Vegas, Nevada 89102
    United States

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    Berlin, New Jersey 08009
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    Site Not Available

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    Cherry Hill, New Jersey 08002
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    Marlton, New Jersey 08053
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    Albuquerque, New Mexico 87109
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    Brooklyn, New York 11229
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    Cary, North Carolina 27511
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    Chapel Hill, North Carolina 27599
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    Charlotte, North Carolina 28211
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    Beachwood, Ohio 44122
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    Dayton, Ohio 45417
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    Middleburg Heights, Ohio 44130
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    Portland, Oregon 97210
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    North Charleston, South Carolina 29405
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    Memphis, Tennessee 38119
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    Dallas, Texas 75231
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    Richardson, Texas 75080
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    Stafford, Texas 77477
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  • Grayline Research Center

    Wichita Falls, Texas 76309
    United States

    Active - Recruiting

  • Core Clinical Research

    Everett, Washington 98201
    United States

    Active - Recruiting

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