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NCT05597241 · ClinicalTrials.gov registry record · Phase 1

Multiple Ascending Dose and Electroencephalography Trial of GATE-202 in Healthy Volunteers

A Phase 1 study of Major Depressive Disorder, sponsored by Syndeio Biosciences.

Completed
Registry status
Phase 1
Development phase
40
Enrollment target
1
Study location

NCT05597241 is a Phase 1 study of Major Depressive Disorder that has completed, run by Syndeio Biosciences. The registered enrollment target is 40 participants, below the 377-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05597241, a Phase 1 study of Major Depressive Disorder, has completed, sponsored by Syndeio Biosciences.

COMPLETED
Registry status
Phase 1
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

To evaluate the safety, tolerability, pharmacokinetics and EEG pharmacodynamics of single and multiple ascending doses of apimostinel in normal human volunteers

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG apimostinel

Study Locations (1)

Arkansas

  • Woodland Research Northwest - Rogers

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2022-10-15
Est. Completion 2023-04-04
Phase Phase 1

Sponsor

Syndeio Biosciences

7 total trials

What the Registry Record Tells You About NCT05597241

The ClinicalTrials.gov registry entry for NCT05597241 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 377-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (89% lower). The listed sponsor is Syndeio Biosciences, which has 7 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Major Depressive Disorder appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT05597241 reports 1 study location spanning 1 distinct geographic area - top geographies include Arkansas.

Frequently Asked Questions

What is clinical trial NCT05597241 about?

NCT05597241 is a clinical study titled "Multiple Ascending Dose and Electroencephalography Trial of GATE-202 in Healthy Volunteers". To evaluate the safety, tolerability, pharmacokinetics and EEG pharmacodynamics of single and multiple ascending doses of apimostinel in normal human volunteers

What is the current status of trial NCT05597241?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2022-10-15. Estimated completion is 2023-04-04.

What conditions does trial NCT05597241 study?

This clinical trial studies the following conditions: Major Depressive Disorder.

What interventions are being tested in trial NCT05597241?

The interventions under investigation include: Placebo (DRUG), apimostinel (DRUG).

Who is sponsoring clinical trial NCT05597241?

This trial is sponsored by Syndeio Biosciences, which has 7 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05597241 being conducted?

This trial has 1 study location across Arkansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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