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NCT Number: NCT03843060

A Phase 1 Study to Assess the Pharmacokinetics of AZD9977 Administered Alone and in Combination With Itraconazole in Healthy Volunteers

This is an open-label, non-randomized, fixed sequence study conducted at a single study center with primary aim to assess the pharmacokinetics (PK) of AZD9977 in healthy volunteers when administered alone and in combination with multiple doses of itraconazole.

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Key information

Conditions

Heart Failure With Preserved Ejection Fraction (HFpEF) Cardiovascular Diseases Heart Diseases Heart Failure

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Research Site

Baltimore, Maryland, 21225, United States

About this study

This is an open-label, non-randomized, fixed sequence study conducted at a single study center with primary aim to assess the pharmacokinetics (PK) of AZD9977 in healthy volunteers when administered alone and in combination with multiple doses of itraconazole. Two types of treatments (treatment period 1 and treatment period 2) will be administered in a fixed order separated by a washout period of 3 days or more. Treatment period 1 will be single dose of AZD9977 (Dose 1) administration, in the fed state, on Day 1 followed by at least 3 days washout period. For treatment period 2, Itraconazole will be administered daily (Dose 2) from Day 4 to Day 8 plus AZD9977 (Dose 1, fed state) will be administered as a single dose on Day 7. Dose of itraconazole has to be taken at -1 hour (1 hour prior to AZD9977 dosing) when co-administered with AZD9977.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Provision of signed and dated, written informed consent prior to any study specific procedures.
  • Healthy male and female participants of non-childbearing potential aged 18 - 55 years with suitable veins for cannulation or repeated venipuncture.
  • Females must have a negative pregnancy test at screening and on admission to the unit, must not be lactating and must be of non-childbearing potential, confirmed at screening by fulfilling one of the following criteria:
  • Postmenopausal defined as amenorrhea for at least 12 months or more following cessation of all exogenous hormonal treatments and follicle stimulating hormone (FSH) levels ≥40 mlU/ml.
  • Documentation of irreversible surgical sterilization by hysterectomy, bilateral oophorectomy or bilateral salpingectomy but not tubal ligation.
  • Have a body mass index (BMI) between 18 and 30 kg/m2 inclusive and weigh at least 50 kg and no more than 100 kg inclusive.

Exclusion criteria

  • History of any clinically significant disease or disorder which, in the opinion of the PI, may either put the volunteer at risk because of participation in the study, or influence the results or the 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.
  • Any clinically significant illness, medical/surgical procedure, or trauma within 4 weeks of the first administration of IMP.

Any clinically significant abnormalities in clinical chemistry, hematology, or urinalysis results, as judged by the PI including serum potassium > 5.0 mmol/L, serum hsTnI > 25.6 pg/mL, and NT-pro-BNP > 124 pg/mL.

  • Any clinically significant abnormal findings in vital signs as specified below and as judged by the PI at screening and on admission including:
  • Systolic blood pressure (SBP) < 90 mmHg or > 140 mmHg.
  • Diastolic blood pressure (DBP) < 50 mmHg or > 90 mmHg.
  • HR < 45 or > 90 beats per minute (bpm). 6. Any clinically significant abnormalities on 12-lead ECG, as judged by the PI.
  • Any positive result on screening for serum hepatitis B surface antigen, hepatitis C antibody, and human immunodeficiency virus (HIV) antibody.
  • Known or suspected history of drug abuse in the last 12 months 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 the 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 the longest.
  • Plasma donation within 1 month of screening or any blood donation/loss more than 500 mL during the 3 months prior to screening.
  • History of severe allergy/hypersensitivity or ongoing allergy/hypersensitivity, as judged by the PI or history of hypersensitivity to drugs with a similar chemical structure or class to AZD9977.
  • Current smokers or those who have smoked or used nicotine products (including e cigarettes) within the 3 months prior to screening.
  • Positive screen for drugs of abuse, cotinine or alcohol at screening or on each admission to the study center.
  • Use of drugs with enzyme-inducing properties such as St John's Wort within 3 weeks prior to the first administration of IMP.
  • Use of any prescribed or non prescribed medication including antacids, analgesics (other than paracetamol/acetaminophen), herbal remedies, megadose vitamins (intake of 20 to 600 times the recommended daily dose) and minerals during the 2 weeks prior to the first administration of IMP or longer if the medication has a long half life.
  • Known or suspected history of alcohol or drug abuse or excessive intake of alcohol in the last 12 months as judged by the PI.
  • Involvement of any AstraZeneca, PAREXEL or study site employee or their close relatives.
  • Participants who have previously received AZD9977. 19. Judgment by the PI that the participant should not participate in the study if they have any ongoing or recent (i.e., during the screening period) minor medical complaints that may interfere with the interpretation of study data or are considered unlikely to comply with study procedures, restrictions, and requirements.
  • Vulnerable participants , e.g., kept in detention, protected adults under guardianship, trusteeship, or committed to an institution by governmental or juridical order.
  • Participants with any special dietary restrictions such as participants that are lactose intolerant or are vegetarians/vegans.
  • Drugs affecting CYP3A4 (itraconazole) should be refrained from use for 3 weeks prior to study commencement and thereafter until study completion.
  • The following exclusion criterion is driven by contraindications from the proposed concomitant CYP3A4 (itraconazole) inhibitor medications: Itraconazole (Sporanox) capsules are contra-indicated in patients with known hypersensitivity to itraconazole or to any of the excipients.

Treatment and study plan

AZD9977

Drug

Participants will receive single AZD9977 (Dose 1) capsule orally once daily in fed state, on Day 1 followed by at least 3 days washout period.

Itraconazole

Drug

Participants will receive Itraconazole daily (Dose 2) capsule orally once daily from Day 4 to Day 8 plus will be administered AZD9977 (Dose 1, fed state) as a single dose on Day 7. Dose of itraconazole has to be taken at -1 hour (1 hour prior to AZD9977 dosing) when co-administered with AZD9977.

Other names: Sporanox

Primary outcomes

  1. Area under plasma concentration-time curve from time zero to infinity (AUC) for AZD9977

    Time frame: Day 1 to 3: Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose. Day 4 to 9: pre-dose on Day 7 and 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose

    To access pharmacokinetics (PK) of AZD9977 in healthy volunteers when administered alone and in combination with multiple doses of itraconazole

  2. Area under the plasma concentration-time curve from time zero to time of last quantifiable concentration (AUClast) for AZD9977

    Time frame: Day 1 to 3: Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose. Day 4 to 9: pre-dose on Day 7 and 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose

    To access pharmacokinetics (PK) of AZD9977 in healthy volunteers when administered alone and in combination with multiple doses of itraconazole

  3. Maximum observed plasma concentration (Cmax) for AZD9977

    Time frame: Day 1 to 3: Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose. Day 4 to 9: pre-dose on Day 7 and 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose

    To access pharmacokinetics (PK) of AZD9977 in healthy volunteers when administered alone and in combination with multiple doses of itraconazole

Secondary outcomes

  1. Time to reach Maximum Observed Plasma Concentration (tMax)

    Time frame: Day 1 to 3: Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose. Day 4 to 9: pre-dose on Day 7 and 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose

    To access pharmacokinetics (PK) of AZD9977 in healthy volunteers when administered alone and in combination with multiple doses of itraconazole

  2. Half-life associated with terminal slope (λz) of a semi-logarithmic concentration-time curve (t½λz)

    Time frame: Day 1 to 3: Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose. Day 4 to 9: pre-dose on Day 7 and 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose

    To access pharmacokinetics (PK) of AZD9977 in healthy volunteers when administered alone and in combination with multiple doses of itraconazole

  3. Mean residence time of the unchanged drug in the systemic circulation from time zero to infinity (MRT)

    Time frame: Day 1 to 3: Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose. Day 4 to 9: pre-dose on Day 7 and 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose

    To access pharmacokinetics (PK) of AZD9977 in healthy volunteers when administered alone and in combination with multiple doses of itraconazole.

  4. Terminal elimination rate constant (λz)

    Time frame: Day 1 to 3: Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose. Day 4 to 9: pre-dose on Day 7 and 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose

    To access pharmacokinetics (PK) of AZD9977 in healthy volunteers when administered alone and in combination with multiple doses of itraconazole

  5. Apparent total body clearance of drug from plasmsa after extravascular administration (CL/F)

    Time frame: Day 1 to 3: Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose. Day 4 to 9: pre-dose on Day 7 and 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose

    To access pharmacokinetics (PK) of AZD9977 in healthy volunteers when administered alone and in combination with multiple doses of itraconazole

  6. Apparent volume of distribution during the terminal phase after extravascular administration (Vz/F)

    Time frame: Day 1 to 3: Pre-dose, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose. Day 4 to 9: pre-dose on Day 7 and 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 8, 12, 16, 24, 36 and 48 hours post-dose

    To access pharmacokinetics (PK) of AZD9977 in healthy volunteers when administered alone and in combination with multiple doses of itraconazole

  7. Number of participants with adverse events (AEs)

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess AEs as variable of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  8. Number of participants with abnormal blood pressure (both systolic and diastolic blood pressure)

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To measure BP as variable of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole. BP will be collected after the participants has rested in the supine position for at least 5 minutes.

  9. Number of participants with abnormal pulse rate

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To measure pulse rate as variable of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole. Pulse rate will be collected after the participants has rested in the supine position for at least 5 minutes.

  10. Number of participants with abnormal 12-lead Electrocardiograms (ECG)

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To examine the safety and tolerability of AZD9977 in combination with itraconazole. 12-lead safety ECG will be obtained after the participant rested in the supine position for at least 10 minutes using the sites own ECG machines. The Principal Investigator (PI) will judge the overall interpretation as normal or abnormal and this evaluation will be reported in ClinBase. If abnormal, it will be further documented as to whether or not the abnormality is clinically significant by the PI.

  11. Number of participants with abnormal physical examination findings

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess any clinically significant abnormal physical examination findings as a variable of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole. The complete physical examinations will include an assessment of the general appearance, respiratory, cardiovascular, abdomen, skin, head, and neck (including ears, eyes, nose, and throat), lymph nodes, thyroid, musculoskeletal and neurological systems. The brief physical examinations will include an assessment of the general appearance, skin, abdomen, cardiovascular system and respiratory.

  12. Number of participants with abnormal laboratory assessments: Hematology- White blood cell (WBC) count

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the white blood cell count as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole

  13. Number of participnats with abnormal laboratory assessments: Hematology- Red blood cell (RBC) count

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the red blood cell count as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole

  14. Number of paticipants with abnormal laboratory assessments: Hematology - Hemoglobin (Hb)

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the Hb as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole

  15. Number of participants with abnormal laboratory assessments: Hematology - Hematocrit (HCT) and Reticulocyte absolute count

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the HCT and reticulocyte absolute count as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  16. Number of participants with abnormal laboratory assessments: Hematology - Mean corpuscular hemoglobin (MCH)

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the MCH as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  17. Number of participants with abnormal laboratory assessments: Hematology - Mean corpuscular volume (MCV)

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the MCV as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  18. Number of participants with abnormal laboratory assessments: Hematology - Mean corpuscular hemoglobin concentration (MCHC)

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the MCHC as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  19. Number of participants with abnormal laboratory assessments: Hematology- Neutrophils absolute count

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the neutrophils absolute count as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole

  20. Number of participants with abnotmal laboratory assessments: Hematology- Lymphocytes absolute count

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the Lymphocytes absolute count as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole

  21. Number of participants with abnormal laboratory assessments: Hematology- Monocytes absolute count

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the Monocytes absolute count as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole

  22. Number of participants with abnormal laboratory assessments: Hematology- Eosinophils absolute count

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the Eosinophils absolute count as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole

  23. Number of participants with abnormal laboratory assessments: Hematology- Basophils absolute count

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the Basophils absolute count as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole

  24. Number of participants with abnormal laboratory assessments: Hematology- Platelets count

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the Platelets count as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole

  25. Number of participants with abnormal laboratory assessments: Serum Clinical chemistry - Calcium, potassium, phosphate and sodium

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the serum calcium, potassium, phosphate and sodium level as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  26. Number of participants with abnormal laboratory assessments: Serum Clinical chemistry - Liver enzymes

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the serum Alanine aminotransferase (ALT), Alkaline phosphatase (ALP), Aspartate aminotransferase (AST) and Gamma glutamyl transpeptidase (GGT) level as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  27. Number of participants with abnormal laboratory assessments: Serum Clinical chemistry - Albumin

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the albumin level as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  28. Number of participants with abnormal laboratory assessments: Serum Clinical chemistry - C reactive protein (CRP)

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the CRP level as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazol

  29. Number of participants with abnormal laboratory assessments: Serum Clinical chemistry - Creatine kinase (CK)

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the CK level as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  30. Number of participants with abnormal laboratory assessments: Serum Clinical chemistry - Creatinine

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the creatinine level as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  31. Number of participants with abnormal laboratory assessments: Serum Clinical chemistry - Glucose (fasting)

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the fasting glucose level as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  32. Number of participants with abnormal laboratory assessments: Serum Clinical chemistry- Uric acid

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the uric acid level as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  33. Number of participants with abnormal laboratory assessments: Serum Clinical chemistry- BUN

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the BUN level as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  34. Number of participants with abnormal laboratory assessments: Serum Clinical chemistry - Total Bilirubin (TBL)

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the TBL level as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  35. Number of participants with abnormal laboratory assessments: Serum Clinical chemistry - Indirect bilirubin

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the indirect bilirubin as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  36. Number of participants with abnormal laboratory assessments: Serum Clinical chemistry - High-sensitivity troponin I ((hsTnI)

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the High-sensitivity troponin I ((hsTnI) as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  37. Number of participants with abnormal laboratory assessments: Serum Clinical chemistry - N-terminal-pro-brain natriuretic peptide (NT-pro-BNP)

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the N-terminal-pro-brain natriuretic peptide (NT-pro-BNP) as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

  38. Number of participants with abnormal laboratory assessments: Clinical Urinalysis - Protein

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the urine protein level as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole. If urinalysis is positive for protein, a microscopy test will be performed to assess RBC, WBC, casts [cellular, granular, hyaline]).

  39. Number of participants with abnormal laboratory assessments: Clinical Urinalysis - Blood

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the urine blood level as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole. If urinalysis is positive for blood, a microscopy test will be performed to assess RBC, WBC, casts [cellular, granular, hyaline]).

  40. Number of participants with abnormal laboratory assessments: Clinical Urinalysis - Glucose

    Time frame: From screening (Day -28) till follow-up visit (up to approximately 6 weeks)

    To assess the urine glucose level as variables of safety and tolerability after administration of single dose of AZD9977 in combination with itraconazole.

Sponsors and collaborators

Lead sponsor

AstraZeneca

Industry

Registry information

Official study title

A Phase 1 Single Center Open-label, Non-randomized, Fixed Sequence Study in Healthy Volunteers to Assess the Pharmacokinetics (PK) of AZD9977 When Administered Alone and With Itraconazole

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Feb 15, 2019
Registry last updated
Apr 22, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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