Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01989520
Other study ID # D3551C00002
Secondary ID
Status Completed
Phase Phase 1
First received November 15, 2013
Last updated June 24, 2015
Start date January 2014
Est. completion date April 2014

Study information

Verified date June 2015
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Medicines and Healthcare Products Regulatory Agency
Study type Interventional

Clinical Trial Summary

Study to investigate relative bioavailability of up to five different formulations of AZD5069


Description:

An Open-label, Single Centre Relative Bioavailability Study With an Adaptive Design Comparing up to 5 Solid Oral AZD5069 Formulations After Single Dose Administration to Healthy Volunteers


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date April 2014
Est. primary completion date April 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

1. Healthy male and/or female volunteers aged 18 to 50 years (inclusive).

2. Non-smokers or ex-smokers with no smoking history for the last 3 months prior to screening.

3. Body mass index (BMI) =18.0 and =30.0 kg/m2 calculated from height and weight at screening; minimum (min) weight 50 kg and maximum (max) weight 100 kg.

4. Healthy volunteers with neutrophil counts within the laboratory range at screening.

Exclusion Criteria:

1. A definite or suspected personal history of severe allergy, intolerance or hypersensitivity or ongoing allergy to drugs with a similar chemical structure or class to AZD5069 and/or the excipients, as judged to be clinically relevant by the Investigator.

2. Healthy volunteers who have previously received AZD5069.

3. Volunteers with latent tuberculosis as suggested by their history and judged by the Investigator; confirmatory testing with eg, Quantiferon(R) -TB Gold may be done if required.

4. Volunteers who have received live or live-attenuated vaccine in the 2 weeks prior to the first administration of the IP -

Study Design

Allocation: Randomized, Endpoint Classification: Bio-availability Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms

  • Uncontrolled and Persistent Asthma

Intervention

Drug:
Phase IIb formulation
Single oral dose 45mg AZD5069
Putative phase III formulation
Single oral dose 45mg AZD5069
Slow dissolution variant 1
Single oral dose 45mg AZD5069
Slow dissolution variant 2
Single oral dose 45mg AZD 5069
Test treatment E
Tablet formulation E, 45 mg (intermediate dissolution variant) of AZD5069

Locations

Country Name City State
United Kingdom Research Site London

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Description of pharmacokinetics of AZD5069 and its metabolite in terms of area under plasma concentration-time curve from time zero to the time of last quantifiable analyte concentration and extrapolated to infinity (AUC(0-last) and AUC) Curve taken during each of the 5 treatments Samples taken predose and 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, and 24 hours postdose No
Primary Description of pharmacokinetics of AZD5069 and its metabolite in terms of observed maximum plasma concentration (Cmax), plasma concentration measured at 12 hours (C12h), Cmax/C12h ratio, Cmax/AUC ratio, terminal rate constant (?z) Curve taken during each of the 5 treatments Sample taken predose and 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, and 24 hours postdose No
Primary Description of pharmacokinetics of AZD5069 and its metabolite in terms of terminal half-life (t½?z), time to reach maximum plasma concentration (tmax) Curve taken during each of the 5 treatments Sample taken predose and 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, and 24 hours postdose No
Primary Description of pharmacokinetics of AZD5069 and its metabolite in terms of apparent systemic clearance (CL/F) (AZD5069 only), and apparent volume of distribution (Vz/F) (AZD5069 only) Curve taken during each of the 5 treatments Sample taken predose and 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, and 24 hours postdose No
Secondary Description of effect on neutrophils in terms of circulating neutrophil numbers reported as absolute circulating neutrophil counts (ANC). The minimum absolute neutrophil count (ANCmin) and the time to ANCmin (ANCtmin) Samples taken during each of the 5 treatments Baseline sample taken at predose day 1 and then 2, 4, 6, 8, 10, 12, and 24 hours postdose Yes
Secondary Description of effect on neutrophils in terms of mean of ANC values from predose to 24 hours postdose (ANCmean), the minimum of the ANC ratio values (ANCmin,ratio) Samples taken during each of the 5 treatments Baseline sample taken at predose day 1 and then 2, 4, 6, 8, 10, 12, and 24 hours postdose Yes
Secondary Description of effect on neutrophils in terms of the mean of ANC ratio values calculated baseline to 24 hours post dose (ANCmean,ratio) Samples taken during each of the 5 treatments Baseline sample taken at predose day 1 and then 2, 4, 6, 8, 10, 12, and 24 hours postdose Yes

External Links