Tricaprilin Liquid Formulation PK Study
NCT05028114 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 71
Last updated 2023-10-17
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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