AZD4635 Relative Bioavailability Study (Rel Bio)

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AstraZeneca

Status and phase

Completed
Phase 1

Conditions

Healthy Volunteers

Treatments

Drug: Lansoprazole and AZD4635 50 mg solid oral formulation
Drug: AZD4635 solid oral formulation variant 2 - fasted
Drug: AZD4635 50 mg nano-suspension (reference)
Drug: AZD4635 solid oral formulation - fed
Drug: AZD4635 solid oral formulation - fasted
Drug: AZD4635 solid oral formulation variant 1 - fasted
Drug: [14C] AZD4635 IV microtracer - fasted

Study type

Interventional

Funder types

Industry

Identifiers

NCT03710434
D8730C00002
2018-003366-14 (EudraCT Number)

Details and patient eligibility

About

To investigate the pharmacokinetics and relative bioavailability of AZD4635 solid oral formulation and compare with the nano-suspension reference formulation with the option to assess food effect, pH effect and absolute bioavailability

Full description

This is a single centre, phase 1, open-label randomised, 2-part study to assess the pharmacokinetics and relative bioavailability of AZD4635 in non-smoking healthy male subjects, with the option to assess food effect, pH effect and absolute bioavailability. It is planned to enrol 20 subjects who will participate in both parts of the study. Subjects will receive a single-dose of AZD4635 in 6 dosing periods with a minimum washout of 9 days between doses. Part A is a 2-period randomised crossover study of single doses of AZD4635. Subjects will be randomised to receive 50mg AZD4635 nano-suspension (reference) or 50mg AZD4635 solid oral formulation, in the fasted state. Part B is a 4-period, open-label, randomised, crossover study of single doses of AZD4635 in the same subjects from Part A. The treatments selected for Part B will depend on the outcome of interim analyses of AZD4635 exposure. Subjects will receive 2 of the following 4 treatments in dosing periods 3 and 4: A single dose of AZD4635 solid oral formulation dose after a high fat meal A single dose of AZD4635 solid oral formulation co-administered with a proton pump inhibitor (PPI), lansoprazole (fasted state) A different single dose (XX mg) of AZD4635 solid oral formulation (fasted state) Another different single dose (YY mg) of AZD4635 solid oral formulation (fasted state) Periods 5 and 6 is a 2-period randomised crossover of two variants of AZD4635 solid oral formulation. Subjects will be randomised to receive AZD4635 solid oral formulation variant 1 in the fasted state or AZD4635 solid oral formulation variant 2 in the fasted state. In Periods 5 and 6, Part B an IV microtracer dose of [14C] AZD4635 with solid oral formulation, variant 1 will be administered.

Enrollment

21 patients

Sex

Male

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Provision of signed and dated, written informed consent prior to any study specific procedures.
  • Healthy male subjects aged 18 to 55 years with suitable veins for cannulation or repeated venepuncture and IV infusion.
  • Have a body mass index of 18.0 to 32.0 kg/m2, and weigh at least 50 kg and no more than 100 kg.
  • Must be willing and able to communicate and participate in the whole study
  • Must agree to adhere to the contraception requirements, as precaution should avoid fathering a child by either true abstinence or use together, with their female partner/spouse, a highly effective contraception form of birth control in combination with a barrier method, starting from the time of AZD4635 administration until 90 days after the last dose of AZD4635.

Exclusion criteria

  • History of any clinically significant disease or disorder which in investigator opinion, may put volunteer at risk because of participation in the study, or influence results of volunteer's ability to participate in the study.
  • History or presence of gastrointestinal, hepatic or renal disease, or any other condition known to interfere with absorption, distribution, metabolism or excretion of drugs.
  • Presence of refractory nausea and vomiting or chronic gastrointestinal diseases.
  • Any clinically significant illness, medical/surgical procedure, or trauma within 4 weeks of the first administration of IMP.
  • Any confirmed clinically significant abnormalities in clinical chemistry, haematology or urinalysis as judged by the investigator
  • Any confirmed clinically significant abnormal findings in vital signs, as judged by investigator.
  • BP >140/90 mmHg or history of hypertension.
  • Any confirmed clinically significant abnormal findings in 12-lead ECG, as judged by investigator.
  • Any positive result at screening for serum hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (HCV Ab) or human immunodeficiency virus (HIV) results.
  • Known or suspected history of drug or alcohol abuse within the past 2 years, as judged by the investigator.
  • Has received another new chemical entity (defined as a compound which has not been approved for marketing) within 3 months of first administration of IMP in this study. The period of exclusion begins 3 months after the final dose or 1 month after the last visit, whichever is longest. Note: subjects consented and screened, but not randomized in this study or a previous Phase I study are not excluded.
  • Plasma donation within 1 month of screening or any blood donation/loss of more than 500 mL of blood during the 3 months prior to screening.
  • History of severe allergy/hypersensitivity or ongoing allergy/hypersensitivity, as judged by the investigator or history of hypersensitivity to drugs with a similar chemical structure or class to AZD4635 or the formulation excipients. Hayfever is allowed unless it is active.
  • Current smokers and those who have smoked within last 12 months. A breath carbon monoxide reading of greater than 10 ppm at screening and admission.
  • Current users of e-cigarettes and nicotine replacement products and those who have used these products within last 12 months.
  • Positive screen for drugs of abuse at screening or admission to the clinical unit or positive screen for alcohol at screening or admission to the clinical unit.
  • Herbal preparations/medications are not allowed throughout the study. These herbal medications include, but are not limited to, St. John's wort, kava, ephedra (ma huang), gingko biloba, dehydroepiandrosterone, yohimbe, saw palmetto, and ginseng. Subjects should stop using these herbal medications 14 days prior to the first dose of AZD4635.
  • Use of any prescribed or nonprescribed medication including antacids, H2 antagonists, PPI, analgesics (other than paracetamol/acetaminophen up to 4 g/day), vitamins and minerals during the two weeks prior to first administration of IMP or longer if medication has a longer half-life. Exceptions may apply on a case by case basis, if considered not to interfere with the objectives of the study, as agreed by the PI and sponsor's medical monitor.
  • Known or suspected history of alcohol or drug abuse or regular alcohol consumption in males >21 units per week (1 unit = ½ pint beer, or a 25 mL shot of 40% spirit, 1.5 to 2 Units = 125 mL glass of wine, depending on type)
  • Subjects who are study site employees, or immediate family members of a study site or sponsor employee
  • Subjects who have previously been enrolled in this study or have previously received AZD4635.
  • Radiation exposure, including that from the present study, excluding background radiation but including diagnostic x-rays and other medical exposures, exceeding 5 mSv in the last 12 months or 10 mSv in the last 5 years. No occupationally exposed worker, as defined in the Ionising Radiation Regulations 2017, shall participate in the study
  • Subjects who have been enrolled in an ADME study in the last 12 months.
  • Subjects with Gilberts Syndrome or a history of cholecystectomy or gall stones.
  • Judgment by investigator that volunteer should not participate in study if they have any ongoing or recent (ie, during the screening period) minor medical complaints that may interfere with the interpretation of the study data or are considered unlikely to comply with the study procedures, restrictions and requirements.
  • Failure to satisfy the investigator of fitness to participate for any other reason.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

21 participants in 8 patient groups

Part A - nano-suspension
Experimental group
Description:
Subjects will receive single dose of AZD4635 50mg nano-suspension (reference) in the fasted state.
Treatment:
Drug: AZD4635 50 mg nano-suspension (reference)
Part A - solid oral formulation
Experimental group
Description:
Subjects will receive single dose of AZD4635 50mg solid oral formulation, in the fasted state.
Treatment:
Drug: AZD4635 solid oral formulation - fasted
Part B-solid oral formulation with food
Experimental group
Description:
Subjects will receive a single dose AZD4635 solid oral formulation after high fat meal.
Treatment:
Drug: AZD4635 solid oral formulation - fed
Part B - solid oral formulation with PPI
Experimental group
Description:
Subjects will receive 30 mg lansoprazole BID and a single dose of AZD4635 solid oral formulation in the fasted state.
Treatment:
Drug: Lansoprazole and AZD4635 50 mg solid oral formulation
Part B - dose exploration 1
Experimental group
Description:
If dose adjustment is required, subjects will receive a different single dose (XX mg) of AZD4635 solid oral formulation, in the fasted state.
Treatment:
Drug: AZD4635 solid oral formulation - fasted
Part B - dose exploration 2
Experimental group
Description:
If dose adjustment is required, subjects will receive a different single dose (YY mg) of AZD4635 solid oral formulation, in the fasted state.
Treatment:
Drug: AZD4635 solid oral formulation - fasted
Part B - variant 1
Experimental group
Description:
Subjects will receive a single dose of AZD4635 solid oral formulation, variant 1 in the fasted state and optional [14C] AZD4635 IV microtracer.
Treatment:
Drug: [14C] AZD4635 IV microtracer - fasted
Drug: AZD4635 solid oral formulation variant 1 - fasted
Part B - variant 2
Experimental group
Description:
Subjects will receive a single dose of AZD4635 solid oral formulation, variant 2 in the fasted state.
Treatment:
Drug: AZD4635 solid oral formulation variant 2 - fasted

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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