Dosing Obese With Noxafil® Under a Trial (DONUT)

Radboud University Medical Center

Status and phase: Completed; Phase 4

Conditions: Morbid Obesity

Treatments: Drug: Posaconazole Injection [Noxafil] 400mg; Drug: Posaconazole Injection [Noxafil] 300mg

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT03246386

UMCN-AKF-17.08

Details and patient eligibility

About

Although posaconazole is approved for the prophylaxes and treatment of invasive fungal infections, specific dosing guidelines for posaconazole in (morbidly) obese patients are not specified. There is clear evidence indicating that heavier patients are receiving a sub-optimal dose if the current guidelines are used. Specifically in the setting of augmented prevalence of species with intermediate susceptible to posaconazole, adequate dosing is needed at start of treatment.

Therefore it seems prudent to conduct a trial in a cohort of obese patients who receive posaconazole (300mg or 400mg) and define the pharmacokinetics. These will then be compared to the pharmacokinetics in a normal-weight group receiving 300mg posaconazole.

Full description

Obese patients with a BMI ≥ 35 kg/m2 undergoing endoscopic gastric bypass surgery will receive a 300 mg or 400mg dose of posaconazole. A PK curve will be determined after administration at t=0.45, 0.75, 1, 1.5, 2, 4, 8, 12, 24, and (if feasible) 48 hours post infusion. Blood samples (4 mL) on PK days will be taken to obtain at least 2.0 mL of plasma.

Enrollment: 24 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Subjects BMI:

   • obese groups: subject must have a BMI ≥35 kg/m2 at the time of inclusion,
   • non-obese group: subject must have a BMI ≥18.5 and < 25kg/m2 at the time of inclusion.

2. Subject is at least 18 of age on the day of screening and not older than 65 years of age on the day of dosing;

3. If a woman, is neither pregnant nor able to become pregnant and is not nursing an infant;

4. Subject is able and willing to sign the Informed Consent before screening evaluations.

   For the non-obese subjects the following additional inclusion criteria applies:

5. Subject is in good age-appropriate health condition as established by medical history, physical examination, electrocardiography, results of biochemistry, hematology and urinalysis testing within 6 weeks prior to study drug administration. Results of biochemistry, hematology and urinalysis testing should be within the laboratory's reference ranges (see Appendix A). If laboratory results are not within the reference ranges, the subject is included based on the investigator's judgment that the observed deviations are not clinically relevant. This should be clearly recorded;

Exclusion criteria

1. Documented history of sensitivity to medicinal products or excipients similar to those found in the posaconazole preparation;
2. History of, or known abuse of drugs, alcohol or solvents (up until a maximum of three months before study drug administration);
3. Use of medication that has known relevant interaction with study drug as determined by the investigator up to 1 weeks prior to study drug administration.
4. Donation of blood or plasma to a blood bank or in a clinical study (except a screening visit) within 4 weeks prior to study drug administration;
5. Blood transfusion within 8 weeks prior to study drug administration;

Trial design

Primary purpose: Basic Science

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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24 participants in 2 patient groups

Obese subjects

Experimental group

Description:

Subjects with a BMI\>35 kg/m2

Treatment:

Drug: Posaconazole Injection [Noxafil] 300mg

Drug: Posaconazole Injection [Noxafil] 400mg

Non-obese subjects

Active Comparator group

Description:

Subjects with a BMI\>18.5 and \<25 kg/m2

Treatment:

Drug: Posaconazole Injection [Noxafil] 300mg