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A Study of the Efficacy and Safety of SP-624 in the Treatment of Adults With Major Depressive Disorder
NCT06254612 · Sirtsei Pharmaceuticals, Inc.
In plain English
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Official title
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
About this study
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
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 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.
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, 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.
* 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).
Study design
Enrollment target: 456 participants
Allocation: randomized
Masking: quadruple
Age groups: adult, older_adult
Timeline
Starts: 2024-03-25
Estimated completion: 2026-07-01
Last updated: 2026-04-01
Interventions
Drug: SP-624Drug: Placebo
Primary outcomes
- • Change from Baseline in the Montgomery-Asberg Depression Rating Scale (MADRS) total score. (Baseline to Week 4)
Sponsor
Sirtsei Pharmaceuticals, Inc. · industry
With: Rho, Inc.
Contacts & investigators
ContactYuki Prescott · contact · yprescott@arrivobio.com · 919-460-9500
InvestigatorGreg Rigdon, PhD · study_director, Sirtsei Pharmaceuticals, Inc.
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