Open Label Pharmacokinetic Study of OZ439 and Piperaquine on Administration of OZ439+TPGS Granules for Oral Suspension Alone or With Either Piperaquine Phosphate Tablets or Granules for Oral Solution in Healthy Volunteers

Malaria Clinical Trial

Official title:

Open Label Pharmacokinetic Study of OZ439 and Piperaquine Following Administration of OZ439+TPGS Granules for Oral Suspension Alone or With Either Piperaquine Phosphate Tablets or Granules for Oral Solution in the Fasted State in Healthy Volunteers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01958619
• Other study ID #: MMV_OZ439_13_004
• Secondary ID: 2013-003409-25
• Status: Completed
• Phase: Phase 1
• First received: October 7, 2013
• Last updated: April 21, 2015
• Start date: October 2013
• Est. completion date: January 2014

Study information

• Verified date: April 2015
• Source: Medicines for Malaria Venture
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency
• Study type: Interventional

Clinical Trial Summary

A healthy volunteer study to characterise the exposure of the two study medications, following administration of OZ439 + TPGS granules with piperaquine phosphate granules (intended for children) and with piperaquine phosphate tablets (intended for adults). Ideally, to confirm the exposure demonstrated in an earlier bioavailability study.

Description:

A Phase 1 open label parallel group, four arm study conducted in healthy male and female subject aged 18 to 55 years of age. Subjects will receive either treatment A, B, C or D as described below:

• Treatment A: 1440 mg PQP tablets and 800 mg OZ439 + TPGS granules for oral suspension

• Treatment B: 960 mg PQP tablets and 800 mg OZ439 + TPGS granules for oral suspension

• Treatment C: 960 mg PQP granules for oral solution and 800 mg OZ439 + TPGS granules for oral suspension

• Treatment D: 800 mg OZ439 + TPGS granules for oral suspension

Recruitment information / eligibility

• Status: Completed
• Enrollment: 55
• Est. completion date: January 2014
• Est. primary completion date: January 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• healthy, male or female, any race aged 18-55 years at screening

• body mass index of 18-30kg/m2 inclusive; and a total body weight >50kg and up to 100kg at screening

• Females must have negative pregnancy test at screening, be non-lactating and of non-childbearing potential confirmed by:

• natural (spontaneous) post-menopausal defined as amenorrheic for 12 months without an alternative medical cause with a screening FSH level >25IU/L for post menopause

• irreversible surgical sterilisation by bilateral oophorectomy or bilateral salpingectomy but not tubal ligation (with or without hysterectomy) at least six months ago

• Must agree to use acceptable methods of contraception Males must use acceptable methods of contraception if the male subject's partner could become pregnant from the time of the first administration of treatment or study medication until 3 months following administration of the last dose of study medication

One of the following acceptable methods of contraception must be used:

• Condom & occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/suppository)

• Surgical sterilisation (vasectomy with documentation of azoospermia) and a barrier method (condom or occlusive cap [diaphragm or cervical/vault caps] used with spermicidal foam/gel/film/cream/suppository)

• Female partner uses oral contraceptives (combination oestrogen/progesterone pills), injectable progesterone or subdermal implants and a barrier method (as above)

• Female partner uses medically prescribed topically-applied transdermal contraceptive patch and a barrier method (as above)

• Female partner has had documented tubal ligation (sterilization). In addition, a barrier method (as above) must be used

• Female partner has had documented placement of an intrauterine device or system and the use of a barrier method (as above)

• True abstinence: when in line with the preferred and usual lifestyle of the subject. Periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception. Abstinent subjects must agree use one of the above-mentioned contraceptive methods, if sexual relationships start during the study or up to 90 days after the last dose of study drug

• Subjects should not donate egg and sperm from the time of administration of study medication until 3 months after study medication

• Must be capable of understanding and complying with the requirements of the protocol and must have signed the informed consent form prior to undergoing any study-related procedures

Exclusion Criteria:

• Male subjects with female partner(s) who is (are) pregnant or lactating from the time of the administration of study medication

• Has a clinically significant disease or any condition or disease that might affect drug absorption, distribution or excretion

• History of allergic reaction to artemisinin-based compounds, 4-aminoquinolines such as piperaquine or any other clinically relevant allergy to drugs or food

• Any clinically significant abnormal laboratory, vital signs or other safety findings as determined by medical history, physical examination or other evaluations conducted at screening or on admission

• History or current evidence of any clinically relevant cardiovascular, pulmonary, hepatic, renal, gastrointestinal (excluding appendectomy and cholecystectomy), haematological, endocrinological, immunological, metabolic, neurological, oncological, psychiatric, urological or other disease, or current infection

• History of post-antibiotic colitis

• Electrocardiogram abnormalities in the 12-lead Electrocardiogram (at screening) and/or 24-hour Holter Electrocardiogram (at screening) which in the opinion of the Investigator is clinically relevant or will interfere with the ECG analysis

• History of clinically significant Electrocardiogram abnormalities, or any of the following abnormalities at screening or on admission:

• PR >200ms

• QRS complex >120ms

• QTcB or QTcF >450ms or shortened QTcB or QTcF less than 340ms for males and females or family history of long QT syndrome or sudden death

• Any degree of heart block (such as first, second or third degree atrioventricular block, incomplete, full or intermittent bundle branch block)

• Abnormal T wave morphology / prominent U waves

• Positive results in any of the serology tests for Hepatitis B Surface Antigen, anti Hepatitis core antibody, Hepatitis C antibodies, and HIV 1 and 2 antibodies

• Confirmed positive results from urine drug screen (amphetamines, benzodiazepines, cocaine, cannabinoids, opiates, barbiturates, and methadone) or from the alcohol breath test at screening and admission

• History or clinical evidence of alcohol abuse, or any recreational drug abuse within the 2 years of screening

• Mentally handicapped

• Participation in a drug trial within 90 days of drug administration

• Use of ANY prescription or over the counter medications, within 3 weeks of study medication administration, or vitamins or herbal supplements within 2 weeks of administration of the study drug, unless prior approval is granted. Intermittent use of paracetamol at doses of up to 2g/day is permitted

• Use of moderate/strong inhibitors and/or inducers of CYP450 in 4 weeks of drug administration (or at least 5 half-lives of the compound whichever is the longer)

• Veins unsuitable for intravenous puncture or cannulation on either arm (veins difficult to locate, access or puncture, or veins with a tendency to rupture during or after puncture)

• Transaminases, bilirubin, serum potassium outside normal range at screening or admission

• Haemoglobin < lower limit of normal at screening or admission

• Donation of >500mL blood in 90 days prior to drug administration

• Must be non-smoker for at least three months before screening. "Tobacco use" includes smoking and the use of snuff and chewing tobacco, and other nicotine containing products. May not use any non-nicotine containing smoking cessation aids, e.g. varenicline, for at least three months before screening

• Any consumption of grapefruit, Seville oranges, wild grapes, black mulberries, pomegranates as fruit juice, marmalade or as a raw fruit within 7 days prior to dosing of study drug and throughout the study

• Any circumstances or conditions, which may affect full participation in the trial or compliance with the protocol

• Legal incapacity or limited legal capacity at screening

• Vegetarians, vegans or any dietary restrictions conflicting with the study standardised menus

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Malaria

Intervention

Drug:
• 1440mg PQP tablets
Piperaquine phosphate tablets (1440mg)
• 960mg PQP tablets
Piperaquine phosphate tablets (960mg)
• 800mg OZ439 + TPGS
OZ439 (800mg) + TPGS granules for oral suspension
• 960mg PQP granules
Piperaquine phosphate granules for oral solution (960mg)

Locations

Country	Name	City	State
United Kingdom	Richmond Pharmacology Ltd.	Croydon	London

Sponsors (2)

Lead Sponsor	Collaborator
Medicines for Malaria Venture	Richmond Pharmacology Limited

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	OZ439 Cmax	OZ439 observed maximum drug plasma concentration	Days 1 pre-dose and post-dose at 0.5, 1, 2, 3, 4, 5, 6, 8, 12, 16 and 24 hours (Day 2), and, 48 (Day 3), 72 (Day 4), 96 (Day 5) and 168 (Day 8) hours post-dose. Sampling will also be done on Day 11, 15, 29 and 43.	No
Primary	OZ439 AUC0-8	OZ439 Area under plasma concentration time curve from time zero extrapolated to infinity.	Days 1 pre-dose and post-dose at 0.5, 1, 2, 3, 4, 5, 6, 8, 12, 16 and 24 hours (Day 2), and, 48 (Day 3), 72 (Day 4), 96 (Day 5) and 168 (Day 8) hours post-dose. Sampling will also be done on Day 11, 15, 29 and 43.	No
Secondary	Piperaquine Cmax	Piperaquine Observed maximum drug plasma concentration	Days 1 pre-dose and post-dose at 0.5, 1, 2, 3, 4, 5, 6, 8, 12, 16 and 24 hours (Day 2), and, 48 (Day 3), 72 (Day 4), 96 (Day 5) and 168 (Day 8) hours post-dose. Sampling will also be done on Day 11, 15, 29 and 43.	No
Secondary	Piperaquine AUC0-8	Piperaquine Area under plasma concentration time curve from time zero extrapolated to infinity.	Days 1 pre-dose and post-dose at 0.5, 1, 2, 3, 4, 5, 6, 8, 12, 16 and 24 hours (Day 2), and, 48 (Day 3), 72 (Day 4), 96 (Day 5) and 168 (Day 8) hours post-dose. Sampling will also be done on Day 11, 15, 29 and 43.	No