Study To Investigate The Relative Bioavailability of OZ439 Formulations In Healthy Volunteers

Healthy Volunteers Clinical Trial

Official title:

A Phase I Study To Investigate The Relative Bioavailability of OZ439 Formulations In Healthy Volunteers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01383096
• Other study ID #: MMV_OZ439_11_001
• Status: Completed
• Phase: Phase 1
• First received: June 23, 2011
• Last updated: January 19, 2015
• Start date: April 2012
• Est. completion date: August 2012

Study information

• Verified date: January 2015
• Source: Medicines for Malaria Venture
• Contact: n/a
• Is FDA regulated: No
• Health authority: Australia: Department of Health and Ageing Therapeutic Goods Administration
• Study type: Interventional

Clinical Trial Summary

This study is designed to assess prototype formulations compared to the aqueous dispersion of Active Pharmaceutical Ingredient used in Phase I and Phase IIa studies to date. It is hoped that the bioavailability of OZ439 can be enhanced in the fasted state to be close to that observed when given after food. This will improve the utility of OZ439 in the field as well as decreasing the cost of treatment (by decreasing the dose of OZ439 required) which is very important for an antimalarial drug product destined for use in developing counties.

Description:

This study was a single centre, open-label, pharmacokinetic, randomized cross-over study in healthy male volunteers and post-menopausal women. This study was conducted over three different cohorts as follows:

Cohort 1: Subjects received a single 800 mg (as free base) dose of five different treatment regimes (treatments A, B, C, D and E) on five occasions.

Cohort 2: Subjects received a single 800 mg (as free base) dose of four different treatment regimes (treatments F, G, H and I) on four occasions.

Cohort 3: Subjects received a single dose, 800mg (as free base) of prototype solution formulation 1 (treatment J) and 400mg (as free base) of prototype solution formulation 1 (treatment K) on two occasions. The treatments were administered under the fasted state.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 52
• Est. completion date: August 2012
• Est. primary completion date: August 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Healthy male and female volunteers between 18 and 55 years (inclusive). Post-menopausal women with amenorrhoea for at least 2 years are eligible confirmed by FSH level >/ = 25microlU/ml

• Body mass Index between 18 and 30 kg/m2, inclusive; and body weight > 50 kg.

• Healthy as determined by pre-study medical history, physical examination (including body temperature), 12 Lead ECG.

• Male volunteers must agree to use a double barrier method of contraception including abstinence, condom plus diaphragm or condom plus IUD or condom plus stable oral/transdermal/injectable hormonal contraceptive by female partner for at least 14 days prior to the time of the first dose of study drug through 90 days after the last dose of study drug and must also agree to not donate sperm for 90 days after the last dose of study drug. Vasectomy with zero sperm count for 6 months minimum prior to the first dose of study drug is an acceptable form of contraception

• Clinical laboratory tests at screening within the reference ranges or if outside the normal range not clinically significant. ALT, AST and total bilirubin must be within the normal range

• Able and willing to give written informed consent

• Willing and able to adhere to the lifestyle guideline requirements

• Willing and able to be confined to the Clinical Research Unit as required by the protocol

Exclusion Criteria:

• Evidence of or history of clinically significant oncologic, pulmonary, hepatic, cardiovascular, hematologic, metabolic, neurological, immunologic, nephrologic, endocrine, psychiatric disease, or current infection

• Evidence of or history of clinically significant gastrointestinal (excluding appendectomy and cholecystectomy) disease or current infection.

• Any condition that could possibly affect drug absorption, e.g. gastrectomy, diarrhea

• History of post-antibiotic colitis

• Pregnancy or breastfeeding

• QTc greater than 450 msec for males and females as corrected by the Fredricia's formula or evidence or history of abnormal cardiac rhythm

• History of drug or alcohol abuse within the past 2 years prior to Screening

• Tobacco users (includes stopping smoking less than 90 days prior to screening. "Tobacco use" includes smoking and the use of snuff and chewing tobacco, and other nicotine containing products

• Received an investigational drug or participated in another research study within 30 days of the first dose of study drug in any part of the study

• Use of prescription drugs within 14 days prior to the first dose of study drug in Period 1, or need for any antibiotic during the study

• Received any non prescription medications, vitamins, herbal supplements or dietary supplements within 7 days of the first dose of study drug in Period 1, unless prior approval is granted. Excluded from this list is intermittent use of acetaminophen at doses of up to 2 g/day

• Consumed alcohol within 72 hours of Day -1 in any part of the study, or have a positive alcohol screen at screening or each admission

• Consumed fruit juice or ate grapefruit within 7 days prior to the first dose of study drug in any part of the study

• Positive test for human immunodeficiency virus, hepatitis B surface antigen or anti-hepatitis C virus

• Positive urine drug screen at Screening or admission

• History of intolerance or hypersensitivity to artemisinins

• Likelihood of requiring treatment during the study period with drugs not permitted by the study protocol

• Volunteers who have donated blood or experienced significant blood loss within 90 days of screening

• Hemoglobin < 13.5 g/dL for males and < 12.5 g/dL for females

• Any concern by the investigator regarding the safe participation of the volunteer or any reason the investigator considers the volunteer inappropriate for participation

Study Design

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

Related Conditions & MeSH terms

• Healthy Volunteers

Intervention

Drug:
• OZ439 mesylate 800mg Powder in Bottle for Oral Suspension
OZ439 800 mg (as free base) as powder in a bottle for reconstitution in a suspension prior to oral administration
• OZ439 mesylate 400mg Prototype Solution Formula 1
OZ439 400 mg (as free base) as a prototype solution formulation 1
• OZ439 mesylate 800mg Prototype Solution Formula 1
OZ439 800 mg (as free base) as a prototype solution formulation 1
• OZ439 mesylate 800mg Prototype Solution Formula 2
OZ439 800 mg (as free base) as a prototype solution formulation 2

Locations

Country	Name	City	State
Australia	AMREP Centre for Clinical Studies	Melbourne	Victoria

Sponsors (3)

Lead Sponsor	Collaborator
Medicines for Malaria Venture	INC Research, Nucleus Network Ltd

Country where clinical trial is conducted

Australia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	OZ439 Cmax	The maximum observed plasma drug concentrations (Cmax)	1, 2, 3, 4, 6, 8, 12, 24, 48, 72, 96 and 168 hours post dosing	No
Primary	OZ439 AUC0-8	Area under the plasma concentration-time curve from zero to infinity (AUC0-8)	1, 2, 3, 4, 6, 8, 12, 24, 48, 72, 96 and 168 hours post dosing	No
Primary	OZ439 t1/2	Apparent terminal half life (t1/2)	1, 2, 3, 4, 6, 8, 12, 24, 48, 72, 96 and 168 hours post dosing	No