Tricaprilin Liquid Formulation PK Study

NCT05028114 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 71

Last updated 2023-10-17

No results posted yet for this study

Summary

The purpose of this study is to evaluate the pharmacokinetics, safety, and tolerability of new liquid formulations of tricaprilin, with the aim of finding a suitable formulation to advance in development. This is a three-part, part-randomised study that include single-dose, food effect, and titration tolerability in up to 80 healthy participants.

Conditions

  • Alzheimer Disease

Interventions

DRUG

AC-1202

Tricaprilin formulated as AC-1202

DRUG

AC-OLE-01

Tricaprilin Formulation

DRUG

AC-OLE-02

Tricaprilin Formulation

DRUG

AC-OLE-03

Tricaprilin Formulation

DRUG

AC-OLE-04

Tricaprilin Formulation

DRUG

AC-OLE-05

Tricaprilin Formulation

DRUG

AC-OLE-06

Tricaprilin Formulation

DRUG

AC-OLE-07

Tricaprilin Formulation

DRUG

AC-OLE-08

Tricaprilin Formulation

DRUG

AC-OLE-09

Tricaprilin Formulation

DRUG

AC-OLE-010

Tricaprilin Formulation

DRUG

AC-OLE-P

Placebo to tricaprilin formulation

Sponsors & Collaborators

  • Cerecin

    lead INDUSTRY

Principal Investigators

  • Study Director · Cerecin

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-08-31
Primary Completion
2022-03-18
Completion
2022-07-19

Countries

  • Australia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05028114 on ClinicalTrials.gov