Major Depressive Disorder (MDD)
Conditions
Brief summary
The purpose of this study is to determine if LY03005 is effective and safe in improve MADRS score, as compared to placebo (no medicine) in participants with Major Depressive Disorder (MDD)
Detailed description
The study consisted of two periods: a screening period of 1 week and a double-blind treatment period (8 weeks). After the screening period, 588 enrolled subjects were randomized into one of 3 study groups in the 1:1:1 ratio, 2 LY03005 treatment groups with different dose or 1 placebo group. Subjects were given investigatory drug or placebo according to the protocol, followed up at the end of 1, 2, 4 6, and 8 weeks.
Interventions
DRUGLY03005 extended-release tablet
orally once a day
DRUGPlacebo
orally once a day
Sponsors
Luye Pharma Group Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
1. Male or female aged 18 to 65 years subjects from outpatients; 2. Subjects currently meet the Diagnostic and Statistical Manual of Manual Disorders, fifth Edition(DSM-5) criteria for MDD with either single or recurrent episodes (296.2/296.3) without psychotic characteristics; 3. Subjects has a total score of the Montgomery- Åsberg Depression Scale (MADRS) ≥26 points at screening; 4. Subjects has a clinical Global Impression -severity illness (CGI-S) score≥4 points at screening
Exclusion criteria
1. Allergic or known to be allergic to venlafaxine and desvenlafaxine; 2. Subjects with MDD who were not responsive to the previous venlafaxine treatment with sufficient amount and duration and to at least two different mechanisms of action antidepressants with adequate amount and duration in the past; 3. There is a clear suicide attempt or behavior and score of the 10th item (suicidal ideation) in MADRS scale is 4 points or greater; 4. Pregnant or lactating women,women who have a planned pregnancy in the near future; 5. Subjects meet the diagnostic criteria for other psychotic disorders(except for MDD) in DSM-5, such as Schizophrenia Spectrum and Other Psychotic Disorders, Bipolar and Related Disorders, Obsessive-Compulsive and related Disorders, post-traumatic stress disorder, separation disorders, anorexia nervosa or bulimia and personality disorder; 6. Subjects who meet the diagnostic criteria for substance or alcohol abuse (excluding nicotine or caffeine) 6 months prior to the screening; 7. MDD secondary to other mental illnesses or physical illnesses; 8. Those with a history of seizures (except for convulsions caused by febrile seizures in children).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Montgomery- Åsberg Depression Rating Scale(MADRS) | 8 Weeks | Changes from baseline in the 10-items Montgomery- Åsberg Depression Scales (MADRS) total scores at the end of treatment. The MADRS has a 10-item checklist. Items are rated on a scale of 0-6, for a total score range of 0 (low severity of depressive symptoms) to 60 (high severity of depressive symptoms). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| 17 items Hamilton Depression Scales (HAM-D17) | 8 Weeks | Changes from baseline in the 17 items Hamilton Depression Scales (HAM-D17) total scores at the end of treatment. HAM-D17 is a standardized, clinician-administered rating scale that assesses 17 items characteristically associated with major depression (symptoms such as depressed mood, guilty feelings, suicide, sleep disturbances, anxiety levels, and weight loss). Nine items are scored on a 3 point scale (0=none/absent to 2=most severe) and 8 items are scored on a 5 point scale (0=none/absent to 4=most severe) for a maximum total score of 50; higher score indicates more depression. |
Countries
China
Outcome results
None listed