Steady-State Comparative Bioavailability Study in Prophylaxis Patients of Lozanoc® 50 mg With Sporanox® 100 mg

Mayne Pharma

Status and phase

Completed

Phase 4

Conditions

Neutropenia

Treatments

Drug: Lozanoc

Drug: Sporanox

Study type

Interventional

Funder types

Industry

Identifiers

NCT02621905

MPG010

Details and patient eligibility

About

The pharmacokinetics of Sporanox and Lozanoc has not been compared in patients requiring anti-fungal prophylaxis or therapy. The present study is designed to compare the pharmacokinetics of Sporanox and Lozanoc in patients requiring primary prophylaxis. The 3-week exposure to each formulation is designed to allow for all participants to reach steady-state for each drug, as the time to steady-state can vary.

Full description

After confirmation of eligibility, participants will be randomly assigned 1:1 to commence therapy with either 100mg mane and 100mg nocte for 21 days or Sporanox 200mg mane and 200mg nocte with food for 21 days. If a subject enters the study already receiving itraconazole prophylaxis at a dose of itraconazole higher than 100 mg twice a day, the subject will then be dosed on study at the pre-study dosage; that is, the subject will take the same number of capsules per day on study as the subject was taking prior to enrolment in the study.

The following information will be collected at baseline; whether the participant is taking itraconazole prophylaxis and at what dose; whether the participant is taking gastric suppression therapy. Patients who are not taking food or who are taking gastric acid suppression therapy (antacids, an H2 antagonist or a proton pump inhibitor) can take Sporanox with cola or orange juice to maximise absorption as recommended in the Sporanox product label (not required for Lozanoc formulation).

At Day 22, participants assigned to

Lozanoc and who have completed 21 days of Lozanoc prophylaxis will cross over to the same number of Sporanox capsules with food for a further 21 days
Sporanox and who have completed 21 days of Sporanox prophylaxis will cross over to the same number of Lozanoc capsules for a further 21 days.

The dose of either drug may be dose-reduced or ceased for toxicity at the discretion of the investigator.

During the course of the treatment periods participants will undergo the following assessments:

Concurrent medication(s)
Clinical adverse events
Measurement of vital signs (weight, blood pressure, temperature)
Targeted physical examination
Documentation of any evidence of systemic fungal infection
Medication and meal diaries
12-lead electrocardiogram (ECG)
Laboratory safety assessments: Renal function and electrolytes (urea, creatinine, estimated glomerular filtration rate [eGFR], sodium, potassium, chloride, bicarbonate), Liver function tests (bilirubin, albumin, total protein, alanine aminotransferase [ALT], aspartate aminotransferase [AST])
Pharmacokinetic testing: Trough (pre-morning dose; 0 hr) sample will be collected at Baseline (Day 1), and at Days 8, 15, 22, 29, 36 and 43. Post-dose samples will also be collected 2, 3.5 and 6 hours after the morning dose on Day 22 and Day 43

Enrollment

40 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Provision of written, informed consent
Age of at least 18 years
No clinical evidence of active systemic fungal infection
Physician-recommended primary prophylaxis against systemic fungal infections with itraconazole in patients who have had or about to have: a heart, lung or bone marrow transplant, combination chemotherapy for cancer; aspergilloma, chronic pulmonary aspergillus bronchitis, or allergic bronchopulmonary aspergillosis
Patients may be receiving itraconazole prophylaxis prior to entry into the study
Body mass index between 15.0 and 35.0 kg/m2

Exclusion criteria

Pregnant, planning pregnancy or breastfeeding
Congestive cardiac failure or other causes of ventricular dysfunction that may outweigh the benefit of itraconazole
Hypersensitivity to either study drug or to any of their excipients
Coadministration of the following drugs:
- CYP3A4 metabolised substrates that can prolong the QT-interval e.g., sertindole, terfenadine
- CYP3A4 metabolised HMG-CoA reductase inhibitors e.g. simvastatin, lovastatin
- Potent CYP3A4 inhibitors e.g. dronedarone
- Triazolam, alprazolam and oral midazolam
- Ergot alkaloids such as dihydroergotamine, ergometrine (ergonovine) and ergotamine