A First in Human Study to Assess the Safety, Tolerability, and Pharmacokinetics of DGX-001
Depressive Disorder
About this trial
This is an interventional treatment trial for Depressive Disorder
Eligibility Criteria
Inclusion Criteria:
- Male or female healthy adult volunteers between 18 to 65 years of age (Both inclusive).
- The subject's BMI is between 18 and 32 kg/m2.
- Female subjects with childbearing potential must have a negative serum pregnancy test.
- The subject is medically healthy with no clinically significant or relevant abnormalities in medical history, physical exam, vital signs, electrocardiogram (ECG), and laboratory evaluations (hematology, chemistry, and urinalysis) as assessed by the Investigator.
Exclusion Criteria:
- The subject has a current or recurrent disease that could affect the action, absorption or disposition of the investigational medicinal product or could affect clinical or laboratory assessments.
- The subject has abnormal renal function test ( <60mL/min, i.e., GFR by Cockroft/Gault) at screening or baseline.
- The subject has evidence of Gilbert's Syndrome or abnormal liver function test (LFTs >1.5x ULN) at screening or baseline.
- The subject has had a cholecystectomy or a history of cholecystitis.
- The subject has clinically significant 12-lead ECG abnormalities, including QTc of 450ms for males and 470ms for females (average of triplicate measures) for any pre-randomization ECG assessment.
- The subject has a current or relevant history of physical or psychiatric illness.
- The subject has a documented history of HIV antibody or tested positive for hepatitis B surface antigen (HBsAg) or Hepatitis C virus (HCV) antibody at screening.
- The subject received an investigational agent within the last 30 days prior to Screening or five half-lives (if known) prior to Screening.
- The subject has a history of alcohol or other substance abuse within the 12 months prior to dosing.
- The subject is currently using any medication (including over-the-counter [OTC], herbal or homeopathic preparations), except for hormonal replacement therapy or hormonal contraceptives, that in the opinion of the investigator can not be discontinued and avoided for four weeks before the first dose throughout the study period.
Sites / Locations
- CMAX Clinical Research Address
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Arm 7
Arm 8
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Single Ascending Dose Cohort S1
Single Ascending Dose Cohort S2
Single Ascending Dose Cohort S3
Single Ascending Dose Cohort S4
Multiple Ascending Doses Cohort M1
Multiple Ascending Doses Cohort M2
Multiple Ascending Doses Cohort M3
Stress Exposure Resilience Panel Cohort 1
Subjects will receive a single dose of either dose level 1 of DGX-001 or placebo
Subjects will receive a single dose of either dose level 2 of DGX-001 or placebo
Subjects will receive a single dose of either dose level 3 of DGX-001 or placebo
Subjects will receive a single dose of either dose level 4 of DGX-001 or placebo
Subjects will receive multiple doses of either dose level 1 of DGX-001 or placebo
Subjects will receive multiple doses of either dose level 2 of DGX-001 or placebo
Subjects will receive multiple doses of either dose level 3 of DGX-001 or placebo
Subjects will receive any of the MAD dose panel or placebo