Last updated: 04/09/2021 08:00:10

A cross-over study to evaluate the effect of itraconazole and rifampicin on the pharmacokinetics (PK) of GSK525762 in healthy female subjects of non child bearing potential

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GSK study ID
204946
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Clinicaltrials.gov ID
NCT02706535
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: A single center, two part, randomized, open label cross-over study to evaluate the effect of itraconazole and rifampicin on the pharmacokinetics of GSK525762 in healthy female subjects of non child bearing potential
Trial description: This is a Phase I, single center, two-part, randomized, open label, cross-over study. Part 1 of this study will evaluate the PK, safety, and tolerability of GSK525762 when administered alone and when co-administered following repeat dosing of itraconazole, a known strong inhibitor of Cytochrome P450 3A4 (CYP3A4) and a Para-glycoprotein (Pgp) inhibitor. Part 1 will consist of 2 Cohorts with preliminary PK and safety data obtained from Cohort 1 informing Cohort 2. Part 2 (one Cohort) of the study will evaluate the PK, safety, and tolerability of GSK525762 when administered alone and when co-administered following repeat dosing of rifampicin, a known potent inducer of CYP3A4. In vitro inhibition data indicate CYP3A4 may be the major route of clearance for GSK525762 and co-administration of drug therapies which modulate CYP3A4 (i.e.CYP3A4 inhibitors and inducers) is likely to alter the exposure of GSK525762 (i.e. increase or decrease exposure, respectively). The data generated from this current study to justify exclusion criteria on concomitant medications which affect CYP3A4 or Pgp and also inform potential dose modification in case of co-administration with medication affecting CYP3A4 activity. All subjects will undergo a screening visit within 28 days of the first dose of study drug followed by one treatment period and a follow-up visit 7-10 days after the last dose of GSK525762. Subjects in Part 1 will participate in the study for up to 45 days and subjects in Part 2 will participate for up to 56 days.
Primary purpose:
Treatment
Trial design:
Crossover Assignment
Masking:
None (Open Label)
Allocation:
Randomized
Primary outcomes:

Part 1: Area under the plasma concentration-time curve (AUC) from pre dose to time ‘t’ (AUC[0-t]) and pre dose to infinite time (AUC[0-infinity]) of GSK525762 and metabolites in the presence and absence of itraconazole

Timeframe: Day 1: Pre dose, 15 min, 30 min, 1 hr, 1.5 hr, 2 hr, 3 hr, 4 hr, 8 hr, 12 hr, 24 hr , 36 hr, and 48 hr post dose. Day 7:Pre dose, 15 min, 30 min, 1 hr, 1.5 hr, 2 hr, 3 hr, 4 hr, 8 hr, 12 hr, 24 hr, 36 hr, 48 hr and 72 hr.

Part 1: Maximum plasma concentration (Cmax) of GSK525762 and metabolites in the presence and absence of itraconazole

Timeframe: Day1 (Pre dose and 15 min, 30 min, 1 hr, 1.5 hr, 2 hr, 3 hr, 4 hr, 8 hr, 12 hr, 24 hr, 36 hr, and 48 hr post dose) and Day7 (Pre dose and 15 min, 30 min, 1 hr, 1.5 hr, 2 hr, 3 hr, 4 hr, 8 hr, 12 hr, 24 hr, 36 hr, 48 hr and 72 hr post dose) of each cohort

Part 1: Time to maximum plasma concentration (tmax) of GSK525762 and metabolites in the presence and absence of itraconazole

Timeframe: Day1 (Pre dose, 15 min, 30 min, 1 hr, 1.5 hr, 2 hr, 3 hr, 4 hr, 8 hr, 12 hr, 24 hr , 36 hr, and 48 hr) and Day7 (Pre dose, 15 min, 30 min, 1 hr, 1.5 hr, 2 hr, 3 hr, 4 hr, 8 hr, 12 hr, 24 hr, 36 hr, 48 hr and 72 hr) of each cohort

Part 2: (AUC[0-t]) and (AUC[0-infinity]) of GSK525762 and metabolites in the presence and absence of rifampicin

Timeframe: Blood samples will be collected on Day1 and Day 18 at Pre dose, 15 min, 30 min, 1 hr, 1.5 hr, 2 hr, 3 hr, 4 hr, 8 hr, 12 hr, 24 hr (Day 19), 36 hr, and 48 hr (Day 20) post dose

Part 2: Cmax of GSK525762 and metabolites in the presence and absence of rifampicin

Timeframe: Blood samples will be collected on Day 1 and Day 18 at Pre dose, 15 min, 30 min, 1 hr, 1.5 hr, 2 hr, 3 hr, 4 hr, 8 hr, 12 hr, 24 hr (Day 19), 36 hr, and 48 hr (Day 20) post dose

Part 2: tmax of GSK525762 and metabolites in the presence and absence of rifampicin

Timeframe: Blood samples will be collected on Day 1 and Day 18 at Pre dose, 15 min, 30 min, 1 hr, 1.5 hr, 2 hr, 3 hr, 4 hr, 8 hr, 12 hr, 24 hr (Day 19), 36 hr, and 48 hr (Day 20) post dose

Secondary outcomes:

Part 1: Number of subjects with adverse event (AE) and serious adverse event (SAE)

Timeframe: Up to 45 days

Part 1: Number of subjects having abnormal haematology parameters as a measure of safety.

Timeframe: Up to 45 days

Part 1: Number of subjects having abnormal clinical chemistry parameters as a measure of safety

Timeframe: Up to 45 days

Part 1: Number of subjects having abnormal urine parameters (using dipstick test) as a measure of safety

Timeframe: Up to 45 days

Part 1: Electrocardiogram (ECG) assessment as a measure of safety and tolerability

Timeframe: Up to 45 days

Part 1: Blood pressure assessment as a safety measure.

Timeframe: Up to 45 days

Part 1: Heart rate assessment as a safety measure.

Timeframe: Up to 45 days

Part 2: Number of subjects with adverse event (AE) and serious adverse event (SAE)

Timeframe: Up to 56 days

Part 2: Number of subjects having abnormal haematology parameters as a measure of safety.

Timeframe: Up to 56 days

Part 2: Number of subjects having abnormal clinical chemistry parameters as a measure of safety.

Timeframe: Up to 56 days

Part 2: Number of subjects having abnormal urine parameters (using dipstick test) as a measure of safety.

Timeframe: Up to 56 days

Part 2: ECG assessment as a measure of safety and tolerability.

Timeframe: Up to 56 days

Part 2: Blood pressure assessment as a safety measure.

Timeframe: Up to 56 days

Part 2: Heart rate assessment as a safety measure.

Timeframe: Up to 56 days

Interventions:
  • Drug: GSK525762 Besylate Tablets
  • Drug: Itraconazole 200 mg
  • Drug: Rifampicin 300 mg
    • Enrollment:
    29
    Primary completion date:
    2017-06-01
    Observational study model:
    Not applicable
    Time perspective:
    Not applicable
    Clinical publications:
    Kylie Riddell, Aarti Patel, Gary Collins, Yanyan Zhou, Dan Schramek, Brandon E. Kremer, and Geraldine Ferron-Brady. An Adaptive PBPK-Driven Design to Investigate the Effect of Itraconazole and Rifampicin on Pharmacokinetics of Molibresib (GSK525762) in Healthy Female Volunteers. J Clin Pharmacol. 2020; DOI: 10.1002/jcph.1711
    Medical condition
    Drug Interactions, Neoplasms
    Product
    itraconazole, molibresib, rifampicin
    Collaborators
    Not applicable
    Study date(s)
    May 2016 to January 2017
    Type
    Interventional
    Phase
    1

    Participation criteria

    Sex
    Female
    Age
    18 - 70 years
    Accepts healthy volunteers
    Yes
    • Between 18 and 70 years of age inclusive, at the time of signing the informed consent.
    • Healthy as determined by the investigator or medically qualified designee based on a medical evaluation including medical history, physical examination, and laboratory tests.
    • ALT and bilirubin >1.5xupper limit of normal (ULN) (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35 percent).
    • Current or chronic history of liver disease, or known hepatic or biliary abnormalities
    Inclusion and exclusion criteria
    Inclusion criteria:
    • Between 18 and 70 years of age inclusive, at the time of signing the informed consent.
    • Healthy as determined by the investigator or medically qualified designee based on a medical evaluation including medical history, physical examination, and laboratory tests.
    • A subject with a clinical abnormality or laboratory parameter(s) which is/are not specifically listed in the inclusion or exclusion criteria, outside the reference range for the population being studied may be included only if the investigator in consultation with the Medical Monitor agree and document that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures.
    • Body Weight >=45 Kilograms (Kg) and body mass index within the range 18.0 – 29.9 Kilograms/squared meter (kg/m^2) (inclusive) at time of screening.

      • Only female subjects of non child bearing potential are eligible for screening; men are not eligible for this study. Female subjects: are eligible to participate if she is not pregnant (as confirmed by a negative serum human chorionic gonadotrophin (hCG) test at screening and serum or urine hCG prior to dosing), is not lactating, and lacks reproductive potential, defined as: •Pre-menopausal females with one of the following: 1. Documented tubal ligation 2. Documented hysteroscopic tubal occlusion procedure with follow-up confirmation of bilateral tubal occlusion 3. Hysterectomy 4. Documented Bilateral Oophorectomy •Postmenopausal defined as 12 months of spontaneous amenorrhea [in questionable cases a blood sample with simultaneous follicle stimulating hormone (FSH) and estradiol levels consistent with menopause (refer to laboratory reference ranges for confirmatory levels)].

    • Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the consent form and in this protocol.
    Exclusion criteria:
    • ALT and bilirubin >1.5xupper limit of normal (ULN) (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35 percent).
    • Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).

      • Cardiac abnormalities as evidenced by any of the following: •History or current untreated clinically significant uncontrolled arrhythmias. •Clinically significant conduction abnormalities or arrhythmias, subjects with Bundle Branch Block •Presence of cardiac pacemaker •History or evidence of current >=Class II congestive heart failure as defined by New York Heart Association (NYHA). •History of acute coronary syndromes (including unstable angina and myocardial infarction), coronary angioplasty, or stenting.

    • Any of the following ECG findings: Baseline QT duration corrected for heart rate by Fridericia’s formula (QTcF) interval >450 miliseconds.
    • History of major gastrointestinal bleeding within the last 6 months. Any evidence of active gastrointestinal bleeding excludes the subject.
    • An unwillingness to abstain from all concomitant medications (excluding acetaminophen).

      • History of regular alcohol consumption within 3 months of the study defined as: •An average weekly intake of >7 drinks for females. One drink is equivalent to 12 grams of alcohol: 12 ounces (360 millilitre [ml]) of beer, 5 ounces (150 ml) of wine or 1.5 ounces (45 ml) of 80 proof distilled spirits.

    • A positive test for alcohol at screening or on admission to the clinical unit.
    • A positive urine drug test at screening or on admission to the clinical unit.
    • Urinary cotinine levels indicative of smoking or history or regular use of tobacco- or nicotine-containing products within 3 months prior to screening.
    • An unwillingness to abstain from caffeine- and xantheine- containing products for 24 hours prior to GSK525762 dosing until collection of the final PK sample during each PK session.
    • An unwillingness to abstain from ingestion of any food or drink containing grapefruit and grapefruit juice, Seville oranges, blood oranges, or pomelos within 7 days prior to the first dose of study treatment(s) or until the end of the study.
    • History of sensitivity to heparin or heparin-induced thrombocytopenia.
    • 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 Medical Monitor, contraindicates their participation.
    • Presence of hepatitis B surface antigen (HBsAg), positive hepatitis C antibody test result at screening or within 3 months prior to first dose of study treatment. A positive pre-study drug/alcohol screen.
    • A positive test for Human Immunodeficiency Virus antibody.
    • Where participation in the study would result in donation of blood or blood products in excess of 500 mL within 56 days.
    • 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 longest).
    • Exposure to more than four new chemical entities within 12 months prior to the first dosing day.

    Trial location(s)

    Location
    Status
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    Location
    GSK Investigational Site
    Baltimore, Maryland, United States, 21225
    Status
    Study Complete
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    Study documents

    Clinical study report
    Available language(s): English
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    Protocol
    Available language(s): English
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    Scientific result summary
    Available language(s): English
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    If you wish to request for full study report, please contact - [email protected]

    Results overview

    Refer to study documents

    Recruitment status
    Study complete
    Actual primary completion date
    2017-06-01
    Actual study completion date
    2017-06-01

    Plain language summaries

    Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.

    Additional information about the trial

    Additional information
    Not applicable
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