First in Man Evaluation of Single and Multiple Doses of Oral ATX2417

Allergy Clinical Trial

Official title:

Double Blind Randomised Placebo Controlled Evaluation of Single and Multiple Oral Doses of ATX2417 in Man and Effect of Food

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02316912
• Other study ID #: ATX2417/001/14
• Status: Completed
• Phase: Phase 1
• First received: December 2, 2014
• Last updated: July 18, 2016
• Start date: February 2015
• Est. completion date: April 2016

Study information

• Verified date: July 2016
• Source: Atopix Therapeutics, Ltd.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency
• Study type: Interventional

Clinical Trial Summary

First in man evaluation of single and multiple doses of compound ATX2417 in healthy male volunteers. A double blind placebo controlled parallel group ascending dose design; up to five dose levels for the single dose and up to two dose levels for the multiple dose (8 days of dosing). Subjects will be screened to assure normal health prior to inclusion in the trial and will be monitored for safety (adverse events, vital signs, ECGs, safety labs) and pharmacokinetic profile. A fasted/fed comparison will also be included in the single ascending dose part of the trial.

Description:

The study consists of two parts, A (single ascending dose including fasted/fed comparison) and B (multiple ascending dose). Part B will be conducted after a thorough review by the Sponsor and the Principal Investigator of the data arising from part A.

Part A This will be a randomised, double blind, placebo controlled, parallel group titration of up to seven single dose levels of ATX2417. In each cohort, six subjects will receive active compound and two will receive placebo in a randomised fashion. At each dose level, 2 subjects (1 subject will receive ATX2417 and 1 subject will receive placebo) will be dosed on Day 1 and the remaining 6 subjects will be dosed at least 24 hours later. Safety and pharmacokinetic observations will be made. There will be a minimum of two weeks between the first dosing day at each dose level. Safety and ATX2417 pharmacokinetic data will be reviewed prior to each dose escalation and, based on pharmacokinetic data, it is also possible to decrease the dose if the pharmacokinetic profile so indicates. This part will also include an assessment of the effect of a high fat breakfast on the absorption and pharmacokinetic profile of ATX 2417, performed at a dose predicted to be associated with therapeutic plasma concentrations.

Part B Following completion of Part A, and selection of appropriate dose levels, Part B will be performed. This will be a randomised, double blind, placebo controlled, parallel group study of up to two dose levels of ATX2417 given once daily for eight days. In each cohort, six subjects will receive active compound and two will receive placebo in a randomised fashion. Safety and pharmacokinetic observations will be made.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 64
• Est. completion date: April 2016
• Est. primary completion date: April 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Healthy male subjects, any racial group

2. Able to comply with the protocol

3. Subjects with a Body Mass Index (BMI) of 21-28 (BMI = Body weight (kg) / (Height (m)2)

Exclusion Criteria:

1. A history of gastrointestinal disorder likely to influence drug absorption

2. Receipt of any medication including over the counter preparations and vitamins within 14 days of the first dose of study drug with the exception of paracetamol up to a maximum of 2 g daily

3. Evidence of clinically significant renal, hepatic, cardiovascular or metabolic dysfunction

4. A history of drug or alcohol abuse

5. Inability to communicate well with the investigator (i.e., language problem, poor mental development or impaired cerebral function)

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator)

Related Conditions & MeSH terms

• Allergy
• Hypersensitivity

Intervention

Drug:
• ATX2417
Randomised double blind parallel group ascending dose assessment
• Placebo
Randomised double blind parallel group ascending dose assessment

Locations

Country	Name	City	State
United Kingdom	Simbec Research	Merthyr Tydfil	Glamorgan

Sponsors (2)

Lead Sponsor	Collaborator
Atopix Therapeutics, Ltd.	Simbec Research

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of subjects with adverse events as a measure of safety and tolerability	Number of subjects with adverse events	120 hours after dosing	No
Secondary	AUC0-t	Area under concentration time curve at 120 hours	120 hours after single dose	No
Secondary	AUC0-t	Area under concentration time curve at 120 hours	120 hours after eighth dose	No