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GSK163090

Phase 2

Depressive Disorder | Small molecule | Psychiatry |GSK plc|Last Updated: Mar 19, 2018

Success Probability

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Trial Design

RandomizedDouble-BlindPLACEBO_CONTROLLED
Total Trials1
Total Enrollment99

FDA Designations

No designations recorded

Clinical trial landscape

GSK163090 · 3 trials · 5 indications

Phase 2 1Phase 1 2
NCT00896363Safety and Efficacy Study in Patients With Major Depressive DisorderDepressive Disorder
COMPLETED99 Analytics
PHASE2COMPLETED
Safety and Efficacy Study in Patients With Major Depressive Disorder
Depressive DisorderUnlock trial analytics

Study Endpoints

Primary Endpoints

Change From Baseline in the Hamilton Depression Rating Scale (HAMD17), on Day 14 and 42
Baseline (Day 1, pre-dose), Day 14 and Day 42

HAMD-17 is a 17-item scale that evaluates depressed mood, vegetative and cognitive symptoms of depression, and co-morbid anxiety symptoms. The 17 items were rated on either a 5-point (0-4) or a 3-point (0-2) scale. In general, the 5 point scale items use a rating of 0=absent; 1=doubtful to mild; 2=mild to moderate; 3=moderate to severe; 4=very severe. The 3-point scale items use a rating of 0=absent; 1=probable or mild; 2=definite. The total HAMD-17score ranges from 0 (not ill) to 52 (severely ill). The highest possible score was 52, which represented the most severe measure of depression; the lowest possible score was 0, which represents an absence of depression. Baseline was defined as the assessment done on Day 1 (pre-dose). Change from baseline in total Score was the difference between HAMD total score at the time point being analyzed to Day 1.

Change From Baseline in Bech Melancholia Subscale (BECH 6) Scale, on Day 14 and 42
Baseline (Day 1, pre-dose), Day 14 and Day 42

The bech melancholia is sum of scores on 6 items- depressed mood, feelings of guilt, work and activities, retardation, anxiety psychic, somatic symptoms general (items 1, 2, 7, 8, 10 and 13 respectively). Each item having 5 responses. The items are rated on a scale of 0-4, where 0=absent; 1=doubtful to mild; 2=mild to moderate; 3=moderate to severe; 4=very severe. Total possible score is 0-24. where the lowest possible score was 0, which represented an absence of depression and higher scores reflecting greater severity of diseases. Baseline was defined as the assessment done on Day 1. Change from baseline was the difference between BECH 6 scale at the time point being analyzed to randomization.

Change From Baseline in Quick Inventory of Depressive Symtomatology - Self Rated (QIDS-SR) Scale, on Day 14 and 42
Baseline (Day 1, pre-dose), Day 14 and Day 42

The QIDS-SR is a 16-item, participant-rated short form of the Inventory of Depressive Symptomatology that assesses 9 domains: sad mood, concentration, self-criticism, suicidal ideation, interest, energy/fatigue, sleep disturbance (initial, middle, and late insomnia or hypersomnia), appetite/weight increase/decrease and psychomotor agitation/retardation. A total score was obtained by summing scores on each domain. the scores ranges from 0 (none) to 27 (very severe), where the highest possible score was 27, which represented the most severe measure of depression; the lowest possible score was 0, which represents an absence of depression. Baseline was defined as the assessment done on Day 1. Change from Randomization in total score was the difference between QIDS total score at the time point being analyzed to randomization.

Number of Participants With Suicidal Behavior and Suicidal Ideation Subscales of the Columbia Suicide Severity Rating Scale (C-SSRS)
Up to Day 52

The C-SSRS was a clinician-rated scale that evaluated severity and change of suicidality by integrating both behaviour and ideation. The 2 of 3 sections of the scale were suicidal behavior and suicidal ideation. For suicidal behaviour participants were scored as non-suicidal-0, preparatory acts or behavior communicating ideation-01, aborted attempt-2, interrupted attempt-3 or actual attempt-4. The score ranges from 0-4, where 0 was absence of suicidal behavior and 4 being the most severe form of suicidal behavior. On the Suicidal Ideation scale, participants were scored as non-suicidal-0, wish to be dead-1, non-specific active suicidal thoughts-2, active suicidal ideation with associated thoughts of methods without intent-3, active suicidal ideation with some intent to act on suicidal thoughts without clear plan-4, active suicidal ideation with plan and intent-5. The score ranges from 0-5, where 0 was absence of suicidal ideation and 5 being the most severe form of suicidal ideation.

Number of Participants With Abnormal Hematology Values of Clinical Concern Range (CCR).
Up to Day 42

Only those parameters for which at least one value of CC was reported were summarized. Pre-defined limits of CC (CC Low \[relative to the lower limit of normal\], CC High \[relative to the upper limit of normal\]) were: hemoglobin (Hb): \> 25, 180; hematocrit (Hct): \> 0.075, 0.54; absolute neutrophil count (ANC): \< 1.5, NA; platelet: \< 100, \> 550; white blood cells (WBC): \< 3,\> 20

Number of Participants With Abnormal Chemistry Values of CCR
Up to Day 42

Only those parameters for which at least one value of CC was reported were summarized. Pre-defined limits of CC (CC Low \[relative to the lower limit of normal\], CC High \[relative to the upper limit of normal\]) were: albumin (unit: gram per liter): \< 30, NA; alanine aminotransferase (ALT): NA, \>= 3 times upper limit of normal; aspartate aminotransferase (AST): NA, \>= 3 times upper limit of normal; total bilirubin: NA, \>=1.5 times upper limit of normal; calcium: \< 2.0, \> 2.75; gamma glutamyl transferase (GGT): \< 3.0, \> 9; potassium: \< 3.0, \> 5.5; magnesium: \< 0.5, \> 1.23.

Change From Baseline in Liver Chemistry -Alkaline Phosphatase (ALP), ALT, AST and GGT
Baseline (screening) up to Day 42

Clinical liver chemistry parameters of Alkaline Phosphatase , ALT, AST, GGT were assessed on screening, Day 7, Day 14, Day 28 and Day 42. Screening was defined as Baseline. Change from Baseline in liver chemistry was the difference between the value at time point analyzed and screening.

Change From Baseline in Liver Chemistry- Direct Bilirubin and Total Bilirubin
Baseline (screening) up to Day 42

Liver chemistry parameters: Direct Bilirubin and Total Bilirubin were assessed on screening, Day 7, Day 14, Day 28 and Day 42. Screening was defined as Baseline. Change from Baseline in liver chemistry was the difference between the value at time point analyzed and screening.

Number of Participant of Urinanalysis Assessment Over Period
Screening (Day -10 to -2), Day 14 and Day 42

Urinalysis parameters included: Urine Occult Blood, Urine Ketones, Urine Ketones. data for number of participants with abnormal urinanalysis parameters was reported by dipstick method. dipstick was a strip used to detect the presence or absence of these parameters in the urine sample. dipstick test gives results in a semi-quantitative manner, and results can be read as negative, Trace, 1+, 2+, and 3+, indicating proportional concentrations in the urine sample. Urine occult blood dipstick and urine general dipstick were semi quantitative results. Urine glucose and urine ketones dipstick results were in milimole per liter, urine protein dipstick results were in gram per liter.

Change From Baseline in Electrocardiogram (ECG) Values -PR Interval, QRS Duration, QT Interval, QTcB, QTcF, RR Interval
Baseline (Day 1) and up to Day 42

Data for change from Baseline was reported for PR Interval, QRS Duration, QT Interval, QTcB, QTcF, and RR Interval. 12-lead ECGs was obtained at each time point during the study using an ECG machine that automatically calculated the heart rate and measures PR, QRS, QT, and QTcB ,QTcF, and RR intervals. Day -1 evening (PM) was the Baseline for participants with only Day -1 records. Day 1 PM Dose was the Baseline for participants with Day 1 records. Baseline was the mean of replicate assessments. Change from Baseline was the difference between the value at the time point analyzed and baseline value.

Mean of Change From Baseline in Systolic and Diastolic Blood Pressure (BP)
Baseline (Day 1) , Day 2, 3, 4, 5, 6, 7, 8, 14, 21, 28 and 42

Semi-supine systolic and diastolic blood pressure was assessed at the specified time points. Measurements were taken after the participant has been semi-supine for at least 5 minutes. BP was measured at least every hour until the values were within the normal range. Day 1 was Baseline and change from Baseline was difference between the value at the time point analyzed and baseline value.

Mean of Change From Baseline in Heart Rate
Baseline (Day 1), Day 2, 3, 4, 5, 6, 7, 8, 14, 21, 28 and 42

Heart rate is the speed of the heartbeat measured by the number of contractions of the heart per minute, (beats per minute). Heart rate was assessed at the specified time points. Measurements were taken after the participant has been semi-supine for at least 5 minutes. Day 1 was Baseline and change from Baseline was difference between the value at the time point analyzed and baseline value.

Number of Participants With All Adverse Events (AEs), and Serious Adverse Events (SAEs)
Up to Day 52

Data for number of participants who presented one or more adverse events (serious or non serious) was reported. An AE was defined as any untoward medical occurrence (MO) in a participant temporally associated with the use of a medicinal product (MP), whether or not considered related to the MP and can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with its use. The SAE was any untoward MO that, at any dose, results in death, life threatening, persistent or significant disability/incapacity, results in or prolongs inpatient hospitalization, congenital abnormality or birth defect, that may not be immediately life-threatening or result in death or hospitalization but may jeopardize the participant or may require medical or surgical intervention to prevent one of the other outcomes listed in this definition.

Safety and tolerability of GSK163090: Clinical laboratory, ECGs and vital signs assessments Questionnaire - DESS(Discontinuation Emergent Signs and symptoms)
All over 10 days post dose for Group 1 and over 3 weeks for subjects in groups 2 and 3.
Brain receptor occupancy of GSK163090 Plasma concentrations of GSK163090
throughout the study

Secondary Endpoints

Mean Last Observed Quantifiable Concentration (Ct) of GSK163090 Over the Period
Day 4 (AM pre-dose), Day 7 (AM and PM pre-dose), Day 10 (AM and PM pre-dose), Day 14 (AM and PM pre-dose), Day 21 (AM pre dose), Day 28 (AM pre dose), Day 42 (AM pre-dose and 4-6 h post AM dose)
Area Under Concentration-time Curve (AUC) at Steady State
Day 4 (AM pre-dose), Day 7 (AM and PM pre-dose), Day 10 (AM and PM pre-dose), Day 14 (AM and PM pre-dose), Day 21 (AM pre dose), Day 28 (AM pre dose), Day 42 (AM pre-dose and 4-6 h post AM dose)
Average Concentration (Cave) at Steady State
Day 4 (AM pre-dose), Day 7 (AM and PM pre-dose), Day 10 (AM and PM pre-dose), Day 14 (AM and PM pre-dose), Day 21 (AM pre dose), Day 28 (AM pre dose), Day 42 (AM pre-dose and 4-6 h post AM dose)
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Study Design & Arms

AllocationRANDOMIZED
MaskingDOUBLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
ActiveACTIVE_COMPARATORParallel Group - High Dose Arm, Low Dose Arm
PlaceboPLACEBO_COMPARATORParallel Group
GSK163090ACTIVE_COMPARATORone infusion only

Interventions

NameTypeDescription
GSK163090 1 mgDRUGDeveloped for the treatment of Major Depressive Disorder
GSK163090 PlaceboDRUGDeveloped for the treatment of Major Depressive Disorder
GSK163090 3 mgDRUGDeveloped for the treatment of Major Depressive Disorder
GSK163090DRUG -
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Eligibility Criteria

Age Range18 Years to 64 Years
SexALL
Healthy VolunteersNo
Study Sites15

Inclusion Criteria: * Currently have severe depression (Major Depressive Disorder - without psychotic features) * meet criteria (DSM IV-TR ) for current major depressive episode for at least 4 weeks but for no greater than 24 months * depression questionnaire (HAMD17) total score greater than or eq...

Countries:RussiaUnited StatesCanada
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Frequently asked questions about GSK163090

What is GSK163090 used for?

GSK163090 is an investigational small molecule being studied for the treatment of major depressive disorder and anxiety disorders. It has been evaluated in clinical trials involving healthy subjects and patients with depressive disorder, including major depressive disorder (MDD). The drug is in Phase 2 clinical development.

What does GSK163090 target?

GSK163090 is a small molecule developed for psychiatric conditions. Its specific molecular target has not been disclosed in available clinical trial information. The drug is being studied for its effects on depressive disorder and anxiety disorders, but the precise mechanism of action is not publicly detailed.

Who makes GSK163090?

GSK163090 is being developed by GSK plc, a global pharmaceutical company listed on the stock exchange under the ticker symbol GSK. The company has conducted clinical trials of this investigational drug for psychiatric indications, including major depressive disorder.

What phase is GSK163090 in?

GSK163090 is in Phase 2 clinical development. It has completed Phase 1 trials and one Phase 2 study in patients with major depressive disorder. The drug is investigational and has not been approved by regulatory authorities for any indication.

What clinical trials is GSK163090 in?

GSK163090 has been studied in four clinical trials. These include NCT00435695, a Phase 1 PET imaging study in healthy males; NCT00536679, a bioavailability and food effect study; NCT00559299, a patient tolerability study; and NCT00896363, a Phase 2 safety and efficacy study in patients with major depressive disorder.

Is GSK163090 the same as other drugs?

GSK163090 is a unique investigational compound developed by GSK plc. No alternative names for this drug have been reported in clinical trial registrations. It is distinct from other marketed antidepressants and is being studied specifically for depressive and anxiety disorders.