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NCT03030105 · ClinicalTrials.gov registry record · Phase 1

Study to Evaluate the Effects of BPN14770 on Scopolamine-induced Cognitive Impairment in Healthy Volunteers

A Phase 1 study, sponsored by Tetra Discovery Partners.

Completed
Registry status
Phase 1
Development phase
38
Enrollment target

NCT03030105: Completed Phase 1 study, sponsored by Tetra Discovery Partners.

NCT03030105 is a Phase 1 study that has completed, run by Tetra Discovery Partners. The registered enrollment target is 38 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (37% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT03030105, a Phase 1 study, has completed, sponsored by Tetra Discovery Partners.

COMPLETED
Registry status
Phase 1
Development phase
38 participants
Enrollment target

Study Summary

This is a Phase 1, randomized, double-blind, placebo-controlled, 6-period crossover study to evaluate the effects of BPN14770 10 mg and 50 mg in reversing scopolamine-induced cognitive impairment in healthy volunteers. A positive control, donepezil 10 mg, will be included, and additivity of BPN14770 50 mg to donepezil 10 mg in reversing scopolamine effects will also be evaluated.

Interventions

  • DRUG Donepezil
  • DRUG BPN14770
  • DRUG BPN14770 placebo
  • DRUG Donepezil placebo
  • DRUG Scopolamine 0.6 MG/ML

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2017-01
Est. Completion 2017-06
Phase Phase 1
Tetra Discovery Partners

8 total trials

What the finished NCT03030105 record still lists

NCT03030105 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 38 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (37% lower).

The record links to 0 conditions, and to 5 interventions - of which Donepezil is the first listed.

NCT03030105 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03030105 about?

NCT03030105 is a clinical study titled "Study to Evaluate the Effects of BPN14770 on Scopolamine-induced Cognitive Impairment in Healthy Volunteers". This is a Phase 1, randomized, double-blind, placebo-controlled, 6-period crossover study to evaluate the effects of BPN14770 10 mg and 50 mg in reversing scopolamine-induced cognitive impairment in healthy volunteers. A positive control, donepezil 10 mg, will be included, and additivity of BPN14770...

What is the current status of trial NCT03030105?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 38 participants. The study started on 2017-01. Estimated completion is 2017-06.

What interventions are being tested in trial NCT03030105?

The interventions under investigation include: Donepezil (DRUG), BPN14770 (DRUG), BPN14770 placebo (DRUG), Donepezil placebo (DRUG), Scopolamine 0.6 MG/ML (DRUG).

Who is sponsoring clinical trial NCT03030105?

This trial is sponsored by Tetra Discovery Partners, which has 8 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03030105's enrollment target sits among peer trials

38 1197th of 2000 higher than 797 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03030105, the US trial registry maintained by the National Library of Medicine. NCT03030105 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.