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Clinical Trials/NCT04618263
NCT04618263
Terminated
Phase 1

A Randomized Double-blind, Placebo-controlled Single and Multiple Intravenous Ascending Dose Study of the Safety, Tolerability and Pharmacokinetics of GATE-101 in Normal Healthy Volunteers

Gate Neurosciences, Inc1 site in 1 country18 target enrollmentOctober 26, 2020

Overview

Phase
Phase 1
Intervention
GATE-101
Conditions
Major Depressive Disorder
Sponsor
Gate Neurosciences, Inc
Enrollment
18
Locations
1
Primary Endpoint
Number of Participants with Treatment-Emergent Adverse Events Through Study Completion, 28 days
Status
Terminated
Last Updated
3 years ago

Overview

Brief Summary

To evaluate the safety, tolerability, and pharmacokinetics of single and multiple ascending doses of GATE-101 in normal human volunteers

Detailed Description

Single ascending dose (SAD), multiple ascending dose (MAD), double-blind placebo-controlled study in normal human volunteers. Secondary objectives: To evaluate the pharmacokinetics (PK) of GATE-101 following increasing single and multiple doses of intravenously (IV) administered GATE-101. GATE-101 or Placebo: Dose/Mode of Administration: Single or 5 Daily Doses;Intravenous

Registry
clinicaltrials.gov
Start Date
October 26, 2020
End Date
August 13, 2021
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Normal, healthy volunteer male and female subjects
  • Aged 18 to 40 years
  • For female subjects must meet one of the following:
  • Surgically sterile or at least 2 years menopausal, confirmed by follicle stimulating hormone (FSH) at screening visit, or,
  • If of childbearing potential, subject must use an acceptable method of birth control from date of screening to at least 30 days after the last dose of study drug. Must have a documented negative blood or urine pregnancy test within 24 hours prior to dosing. If reported sterile or postmenopausal, will be confirmed by FSH.
  • For male subjects, must meet one of the following:
  • Surgically sterile
  • If not surgically sterile then use of an acceptable form of contraception (condom) from the time of randomization through 30 days following the last dose of study drug. Male subjects are strongly advised to inform female partners of the need for them to use highly effective birth control during this time period.
  • Body mass index (BMI) \< 30
  • Clinical laboratory values \<2 times the upper limit of normal (ULN) or deemed not clinically significant by the Investigator.

Exclusion Criteria

  • Human immunodeficiency virus (HIV) infection, or hepatitis or other ongoing infectious disease
  • Evidence of alcohol abuse (greater than 4 units of alcohol on most days; 1 unit = 1/2 pint of beer, 1 glass of wine or 1 oz. of spirits). Alcohol consumption should be avoided for at least 24 hours prior to baseline/dosing visit. A positive alcohol breathalyzer at screening and baseline visit
  • Current abuse of illicit substances, using the Diagnostic and Statistical Manual (DSM) V definition of substance use disorder.
  • Current cigarette/tobacco smoker or use of other tobacco or nicotine products including ecigarettes or vaping (if formerly a smoker must not have smoked for at least one year prior to enrolling in this study). Nonsmoking will be confirmed by cotinine assay.
  • Currently pregnant, planning to become pregnant during the course of the study, or nursing mother
  • Impaired renal function (GFR \< 90 ml/min)
  • Elevated systolic blood pressure (\> 130 mmHg) or diastolic blood pressure (\> 80 mmHg) and/or increased QTc (\>450 msec for men or \>470 msec for women) or additional risk factors for Torsades de Pointes including heart failure, hypokalemia, family history of Long QT Syndrome
  • Type I or Type II diabetes
  • Malignancy in the last 5 years, with the exception of nonmetastatic basal cell or squamous cell carcinoma of the skin or localized carcinoma in situ of the cervix
  • Currently taking prescription (except as listed in Section 7.4.1) or over-the-counter medications including herbal therapies, within 14 days of enrollment into the study.

Arms & Interventions

GATE-101, 15 mg IV, Single Dose, Lumbar Catheter

GATE-101, 15 mg IV, Single Dose, with Lumbar Catheter for collection of cerebrospinal fluid (CSF) PK samples, with follow up of 28 days

Intervention: GATE-101

GATE-101, 5 mg IV, Single Dose

GATE-101, 5 mg IV, Single Dose, with follow up of 28 days

Intervention: GATE-101

GATE-101, 15 mg IV, Single Dose

GATE-101, 15 mg IV, Single Dose, with follow up of 28 days

Intervention: GATE-101

GATE-101, 50 mg IV, Single Dose

GATE-101, 50 mg IV, Single Dose, with follow up of 28 days

Intervention: GATE-101

GATE-101, 150 mg IV, Single Dose

GATE-101, 150 mg IV, Single Dose, with follow up of 28 days

Intervention: GATE-101

GATE-101, 450 mg IV, Single Dose

GATE-101, 450 mg IV, Single Dose, with follow up of 28 days

Intervention: GATE-101

GATE-101, 50 mg IV, Single Dose, Lumbar Catheter

GATE-101, 50 mg IV, Single Dose, with Lumbar Catheter for collection of cerebrospinal fluid (CSF) PK samples, with follow up of 28 days

Intervention: GATE-101

GATE-101 5 mg IV, Five Daily Doses

GATE-101 5 mg IV, Five Daily Doses, with follow up for 28 days from first dose

Intervention: GATE-101

GATE-101 15 mg IV, Five Daily Doses

GATE-101 15 mg IV, Five Daily Doses, with follow up for 28 days from first dose

Intervention: GATE-101

GATE-101 150 mg IV, Five Daily Doses

GATE-101 150 mg IV, Five Daily Doses, with follow up for 28 days from first dose

Intervention: GATE-101

Placebo Comparator, Single Dose

Placebo Comparator, Single Dose, with follow up for 28 days

Intervention: GATE-101

Placebo Comparator, Five Daily Doses

Placebo Comparator, Five Daily Doses, with follow up for 28 days from first dose

Intervention: GATE-101

Outcomes

Primary Outcomes

Number of Participants with Treatment-Emergent Adverse Events Through Study Completion, 28 days

Time Frame: 28 Days

Safety and Tolerabiity

Secondary Outcomes

  • Pharmacokinetics - maximum plasma concentration - following a single intravenous dose(72 hours)
  • Pharmacokinetics - maximum plasma concentration - following 5 daily intravenous doses(72 hours)
  • Pharmacokinetics - area under the curve - following a single intravenous dose(72 hours)
  • Pharmacokinetics - area under the curve - following 5 daily intravenous doses(72 hours)

Study Sites (1)

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