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NCT06254612CompletedPhase 2

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

A Multi-center, Double-Blind, Randomized, Placebo-Controlled Study of the Efficacy and Safety of SP-624 in the Treatment of Adults With Major Depressive Disorder

Source: ClinicalTrials.gov · Last updated 18 Aug 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
497 (actual)
First submitted
2 Feb 2024
Start date
25 Mar 2024
Primary completion date
8 Jul 2026
Lead sponsor
Sirtsei Pharmaceuticals, Inc.
Diseases
Depression
NCT number
NCT06254612

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 497
  • From 25 Mar 2024 to the primary completion date, 8 Jul 2026
  • 50 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • A history of or current DSM-5 diagnosis of MDD with psychotic features, any schizophrenia spectrum and other psychotic disorders, bipolar disorder, or personality disorder.
  • Presence or history of any known clinically significant cardiovascular disorders including, but not limited to: coronary artery disease, heart failure, valvular heart disease, cardiomyopathies, myocardial infarction, chamber enlargement or hypertrophy, or orthostatic hypotension.
  • Presence of uncontrolled hypertension, defined as consistent sitting systolic blood pressure (SBP) \>160 mmHg or consistent sitting diastolic blood pressure (DBP) \>95 mmHg despite present therapy.

Lab values

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

Other

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

Who the study is looking for

  • Males and females, aged 18 to 65 years, inclusive.
  • Meet DSM-5 criteria for moderate to severe MDD, as confirmed by the Mini International 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.

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (50)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
IMA Clinical Research
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AlbuquerqueUnited StatesUnknown status
Accelerated Enrollment Solutions
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AtlantaUnited StatesUnknown status
Donald J Garcia Jr, MD, PA
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AustinUnited StatesUnknown status
Velocity Clinical Research
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BeachwoodUnited StatesUnknown status
Northwest Clinical Research Center
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BellevueUnited StatesUnknown status
Clinical Innovations
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BellflowerUnited StatesUnknown status
NeuroBehavioral Medicine Group
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Bloomfield HillsUnited StatesUnknown status
Boston Clinical Trials
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BostonUnited StatesUnknown status
Integrative Clinical Trials
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BrooklynUnited StatesUnknown status
SanRo Clinical Research Group
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BryantUnited StatesUnknown status
Magnolia Clinical Research
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CaryUnited StatesUnknown status
UNC- Chapel Hill
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Chapel HillUnited StatesUnknown status
New Hope Clinical Research
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CharlotteUnited StatesUnknown status
Center For Emotional Fitness
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Cherry HillUnited StatesUnknown status
MCB Clinical Research Centers
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Colorado SpringsUnited StatesUnknown status
Future Search Trials of Dallas
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DallasUnited StatesUnknown status
Midwest Clinical Research Center
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DaytonUnited StatesUnknown status
Revive Research Institute
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ElginUnited StatesUnknown status
Haracec Clinical Research
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El PasoUnited StatesUnknown status
Core Clinical Research
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EverettUnited StatesUnknown status
Sun Valley Research Center
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ImperialUnited StatesUnknown status
Clinical Neuroscience Solutions
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JacksonvilleUnited StatesUnknown status
Accel Clinical
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LakelandUnited StatesUnknown status
Redbird Research
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Las VegasUnited StatesUnknown status
IMA Clinical Research
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Las VegasUnited StatesUnknown status
Segal Trials
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LauderhillUnited StatesUnknown status
Synergy San Diego
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Lemon GroveUnited StatesUnknown status
Alivation Research
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LincolnUnited StatesUnknown status
CenExel-HRI
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MarltonUnited StatesUnknown status
Tandem Clinical Research
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MarreroUnited StatesUnknown status
Clinical Neuroscience Solutions
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MemphisUnited StatesUnknown status
Velocity Clinical Research
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MeridianUnited StatesUnknown status
Segal Trials - Miami Lakes
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Miami LakesUnited StatesUnknown status
North Star Medical Research
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Middleburg HeightsUnited StatesUnknown status
Pioneer Clinical Research
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New YorkUnited StatesUnknown status
Coastal Carolina Research Center
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North CharlestonUnited StatesUnknown status
Excell Research
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OceansideUnited StatesUnknown status
Clinical Neuroscience Solutions
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OrlandoUnited StatesUnknown status
IMA Clinical Research
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PhoenixUnited StatesUnknown status
DMI Research
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Pinellas ParkUnited StatesUnknown status
Summit Headlands
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PortlandUnited StatesUnknown status
Pillar Clinical Research
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RichardsonUnited StatesUnknown status
CITrials
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RiversideUnited StatesUnknown status
Midwest Research Group
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Saint CharlesUnited StatesUnknown status
R and H Clinical Research
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StaffordUnited StatesUnknown status
Collaborative Neuroscience Research
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TorranceUnited StatesUnknown status
Noble Clinical Research
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TucsonUnited StatesUnknown status
Sunwise Clinical Research
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Walnut CreekUnited StatesUnknown status
Next Level Clinical Trials
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West CovinaUnited StatesUnknown status
Grayline Research Center
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Wichita FallsUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.