Clinical Trials Directory

Trials / Completed

CompletedNCT02958696

Relative Bioavailability of HTL0018318 Oral Aqueous Solution Versus Capsules

A Phase 1, Randomised, Open Label, 2-period Crossover, Single Centre, 3-arm, Single Dose Study to Investigate the Relative Bioavailability of HTL0018318 Oral Aqueous Solution Versus Capsule Formation in Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
37 (actual)
Sponsor
Nxera Pharma UK Limited · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

HTL0018318 is a selective muscarinc M1 agonist. This study is a phase I, open label, randomised, crossover, single dose, trial in healthy volunteers to compare the relative bioavailability of HTL0018318 when given by oral aqueous solution and in capsule formulation.

Conditions

Interventions

TypeNameDescription
DRUGHTL0018318Two single doses of active drug (low, mid or high dose either as aqueous solution or capsule) separated by a washout of at least 12 days.

Timeline

Start date
2016-10-01
Primary completion
2017-01-01
Completion
2017-01-01
First posted
2016-11-08
Last updated
2017-02-03

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02958696. Inclusion in this directory is not an endorsement.