Study Of The Repeat Dosing Of Ketoconazole On The Pharmacokinetics Of A Single Dose Of Pazopanib (GW786034) Eye Drops

NCT00659555 | Completed Phase 1

• 1 other identifier: MD7110861
• Study Type: interventional
• Target: 24
• Locations: 1 country
• Sites: 1

Brief Summary

This is a two-period study to evaluate the effect of repeat oral dosing of ketoconazole on the pharmacokinetics of single dose pazopanib administered as an eye drop

Conditions

Macular Degeneration

Keywords

vascular endothelial growth factor,; drug interaction,; pharmacokinetics,; age-related macular degeneration,; pazopanib,; angiogenesis,; ketoconazole

Outcome Measures

Primary Outcomes (1)

• Pazopanib exposure measured by AUC anc Cmax.

  Up to 2 months

Secondary Outcomes (2)

• General safety measured by clinical laboratory tests, vital signs, cardiac monitoring and AE reporting. Pazopanib exposure as measured by additional pharmacokinetic parameters.

  Up to 2 months

• Additional pharmacokinetic endpoints will include pazopanib AUC(0-t), tmax ans t½.

  Up to 2 months

Study Arms (2)

Treatment A receivers

EXPERIMENTAL

Subjects received pazopanib, single dose as 2 x 40 microliter drops of 5 mg/mL solution in Period 1

Drug: pazopanib eye drops

Treatment B receivers

EXPERIMENTAL

Subjects received ketoconazole, daily 400 mg oral dose on Days 1 to 8; pazopanib, single dose as 2 x 40 microliter drops of 5 mg/mL solution on Day 5 in Period 2

Drug: pazopanib eye drops; Drug: Ketoconozole tablets

Interventions

pazopanib eye drops DRUG

Pazopanib will be administered as eye drop solution via topical ocular route. Pazopanib eye drops will be available as white, colorless solution.

Treatment A receivers; Treatment B receivers

Ketoconozole tablets DRUG

Ketoconozole will be administered as tablets via oral route. Ketoconozole tablets will be present as white, rounded, scored tablets

Treatment B receivers

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Healthy as determined by a trained health care professional, base on a medical evaluation including medical history, physical examination, laboratory tests and 12-lead ECG. A subject with a clinical abnormality or laboratory parameters outside the reference range for the population being studied may be included only if the Investigator and the GSK Medical Monitor agree that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures. Subjects with ALT or AST values above the normal limit should be excluded from enrollment.
• Male or female greater than 18 years of age.
• A female subject is eligible to participate if she is of:
• Non-childbearing potential defined as pre-menopausal females with a document tubal ligation/occlusion or hysterectomy; or postmenopausal defined as 12 months of spontaneous amenorrhea \[in questionable cases a blood sample showing simultaneous follicle stimulating hormone (FSH)\> 40MIU/ml and estradiol \< 40 pg/ml (\<140 pmol/L) may be used to confirm that a woman is postmenopausal\].
• BMI within the range 18-30 kg/m2 (inclusive).
• Capable of giving written informed consent and complying with the requirements and restrictions listed in the consent form.
• QTcB or QTcF \< 450 msec; or QTc \<480 msec in subjects with Bundle Branch Block.

You may not qualify if:

• Current alcohol or illicit drug use which, in the judgment of the Investigator, would interfere with the subject's ability to comply with the dosing schedule or protocol-specified evaluations. For example, a history of regular alcohol consumption (defined below) within 6 months of screening would exclude a subject.
• Regular alcohol consumption: an average weekly intake of \>14 drinks/week for men or \> 7 drinks/week for women. One drink is equivalent to (12 g alcohol) = 5 ounces (150 mL) of wine or 12 ounces (360 mL) of beer or 1.5 ounces (45 ml) of 80 proof distilled spirits.
• A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening.
• HIV requiring treatment during the study period.
• The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
• Exposure to more than four new chemical entities within 12 months prior to the first dosing day.
• Use of prescription, non-prescription, or illicit drugs, including vitamins, herbal and dietary supplements (including St. John's Wort) within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to the first dose of study medication, unless in the opinion of the Investigator and the GSK Medical Monitor the medication will not interfere with the study procedures or compromise subject safety. (Note: this restriction includes ocular prescription and non-prescription drugs.)
• History of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy that, in the opinion of the investigator or GSK Medical Monitor, contraindicates their participation.
• Any contraindication to use of ketoconazole as detailed in the package insert.
• Where participation in the study would result in donation of blood or blood products in excess of 500 ml within a 56 day period.
• Pregnant females as determined by positive urine hCG test at screening or prior to dosing.
• Women planning to breastfeed an infant during the study period.
• Presence of ongoing ocular disease at the time of screening.
• Any eye surgery within three months prior to first dose of study medication.
• An unwillingness to refrain from wearing contact lenses during the study until completion of the follow-up visit.

Sponsors & Collaborators

• GlaxoSmithKline: lead

Study Sites (1)

GSK Investigational Site

Buffalo, New York, 14202, United States

Location

Related Links

• Results for study 110861 can be found on the GSK Clinical Study Register.

MeSH Terms

Conditions

Macular Degeneration

Condition Hierarchy (Ancestors)

Retinal Degeneration; Retinal Diseases; Eye Diseases

Study Officials

• GSK Clinical Trials

  GlaxoSmithKline

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: April 10, 2008
• First Posted: April 16, 2008
• Study Start: April 4, 2008
• Primary Completion: May 10, 2008
• Study Completion: May 10, 2008
• Last Updated: November 13, 2017

Record last verified: 2017-11

Locations

US (1)