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Study to Evaluate the Effect of Food on the Pharmacokinetics of a BGB-3111 in Healthy Subjects

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ClinicalTrials.gov Identifier: NCT04163523
Recruitment Status : Completed
First Posted : November 14, 2019
Last Update Posted : November 14, 2019
Sponsor:
Information provided by (Responsible Party):
BeiGene

Brief Summary:
Phase 1 study in healthy subjects to determine the effect of food on the pharmacokinetics of BGB-3111.

Condition or disease Intervention/treatment Phase
Healthy Volunteers Drug: Zanubrutinib Phase 1

Detailed Description:
A randomized, crossover study to evaluate the effect of food on pharmacokinetics of BGB-3111 when administered in subjects either after a high fat/calorie meal or a low fat/calorie meal or after an overnight fast.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 18 participants
Allocation: Randomized
Intervention Model: Sequential Assignment
Masking: None (Open Label)
Primary Purpose: Basic Science
Official Title: A Single Center, Phase I, Open-Label, Randomized, Crossover Study to Evaluate the Effect of Food on the Pharmacokinetics of a Single Dose of BGB-3111 Given Orally at 320 mg QD in Healthy Adult Subjects
Actual Study Start Date : May 25, 2016
Actual Primary Completion Date : July 21, 2016
Actual Study Completion Date : July 21, 2016

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Treatment Sequence 1
5 Subjects received Period 1- 320 mg BGB-3111 administered after an overnight fast; Period 2- 320 mg BGB-3111 administered after High Fat/Calorie Meal; Period 3 - Day 15: 320 mg BGB-3111 administered after Low Fat/Calorie Meal
Drug: Zanubrutinib
Other Name: BGB-3111

Experimental: Treatment Sequence 2
5 Subjects received Period 1 - Day 1: 320 mg BGB-3111 administered after High Fat/Calorie Meal; Period 2- Day 8: 320 mg BGB-3111 administered after Low Fat/Calorie Meal; Period 3- Day 15: 320 mg BGB-3111 administered after an overnight fast
Drug: Zanubrutinib
Other Name: BGB-3111

Experimental: Treatment Sequence 3
Approximately 5 Subjects receive Period 1-Day 1: 320 mg BGB-3111 administered after Low Fat/Calorie Meal; Period 2-Day 8: 320 mg BGB-3111 administered after an overnight fast; Period 3- Day 15: 320 mg BGB-3111 administered after High Fat/Calorie Meal
Drug: Zanubrutinib
Other Name: BGB-3111




Primary Outcome Measures :
  1. Pharmacokinetic Parameter: Plasma concentration of zanubrutinib as measured by area under concentration-time curve (AUC(0-24)) [ Time Frame: up to 24 hours ]
  2. Pharmacokinetic Parameter: Plasma concentration of zanubrutinib as measured by area under concentration-time curve (AUC(0-∞)) [ Time Frame: up to 2 months ]
  3. Pharmacokinetic Parameter: Peak Plasma Concentration (Cmax) of zanubrutinib [ Time Frame: up to 2 months ]
  4. Pharmacokinetic Parameter: Time to Reach Peak Plasma Concentration (Tmax) of zanubrutinib [ Time Frame: up to 2 months ]
  5. Pharmacokinetic Parameter: Half-life Period of zanubrutinib (T1/2) [ Time Frame: up to 2 months ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Males and females between 18 to 65 years of age (inclusive)
  2. Subjects must be willing and able to give written informed consent by signing an IRB-approved Informed Consent Form prior to admission to this study
  3. Male subjects must agree to use a medically acceptable method of contraception from Screening until 90 days after administration of the last dose of study drug. Medically acceptable methods of contraception include the following: abstinence; a condom in addition to having the female partner use another form of contraception such as medically approved hormonal methods, diaphragm, intrauterine device or a tubal ligation. This requirement may be waived if the Principal Investigator or delegate is satisfied that the subject or partner is sterile (i.e., if female has undergone a hysterectomy, or has undergone a tubal ligation at least 3 months prior to Screening, or is postmenopausal (no menstrual period for at least 12 months prior to Screening); if male has undergone vasectomy at least 6 months prior to Screening). Male subjects agrees not to donate sperm for at least 90 days after administration of the last dose of study drug
  4. Female subjects of non-childbearing potential measures, meeting at least one of the following criteria:

    1. amenorrhoeal for 12 months (menopause confirmed by Follicular Stimulating Hormone (FSH) and Luteinising Hormone (LH) levels as defined by the established reference ranges), or
    2. surgically sterile (e.g. hysterectomy, oophorectomy, tubal ligation for at least 3 months)
  5. Males and females with a body mass Index (BMI) range 18-35 kg/m2 inclusive.
  6. Subjects who are healthy as determined by pre-study medical history, physical examination, and 12-Lead ECG
  7. Subjects who have clinical laboratory test results during the screening period that are within the reference ranges or are clinically acceptable to the Investigator
  8. Subjects who test negative for HIV, HBV, and HCV by standard serologic tests must be negative at Screening
  9. Subjects who test negative for drugs of abuse and alcohol tests at screening and admission
  10. Subjects who are nonsmokers(ex-smokers should have quit smoking at least 6 months prior to screening)

Exclusion Criteria:

  1. Subjects who have a history or presence of respiratory, gastrointestinal, renal, hepatic, hematological, lymphatic, neurological, cardiovascular, psychiatric, musculoskeletal, genitourinary, immunological, dermatological, connective tissue diseases or disorders that, in the Investigator's opinion, could affect the conduct of the study or the absorption, metabolism or excretion of the study drug
  2. Subjects who have a history of relevant drug hypersensitivity
  3. Subjects who have a history of substance abuse, drug addiction or alcoholism
  4. Subjects who consume more than 14 units of alcohol per week for women and 28 units of alcohol for men
  5. A QTc at screening, check-in (all periods), and pre and post study drug dosing of greater than 450 msec for males and females
  6. Subjects with the following laboratory abnormalities (at Screening and check-in of each period): a leucocyte count < 4.0x10^9/L, a neutrophil count of < 2.5x10^9, lymphocyte count < 1.2x10^9/L, Haemoglobin < 10 g/L, or transaminase levels (ALT, AST) > ULN
  7. Subjects who have a significant infection, an acute infection such as influenza, coryzal symptoms, recent upper respiratory tract infection, or known inflammatory process at the time of screening and/or admission
  8. Subjects who have acute gastrointestinal symptoms at the time of screening and/or admission (e.g. nausea, vomiting, diarrhea, heartburn)
  9. Subjects who have used prescription drugs within 14 days of first dosing, unless agreed as nonclinically relevant by the Investigator and BeiGene (hormone replacement therapy will be permitted)
  10. Subjects who have used over the counter medication excluding routine vitamins and herbal supplements (paracetamol <2 grams/day is acceptable) but including mega dose vitamin therapy and St John's Wort within 7 days of first dosing and throughout the study, unless agreed as nonclinically relevant by the Investigator and BeiGene
  11. Subjects who have used any investigational drug and /or participated in any clinical trial within 2 months of first dosing
  12. Subjects who have donated and/or received any blood or blood products within the previous 3 months prior to first dosing. Subjects should not donate blood while on the study and for at least 60 days after last dose of study medication
  13. Subjects who have consumed food or beverage (including caffeine, alcohol, and grapefruit-containing products) known to interfere with cytochrome P450 within 48 hours prior to first study drug dose
  14. Subjects who cannot communicate reliably with the investigator or are unlikely to co-operate with the requirements of the study

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04163523


Locations
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Australia, South Australia
CMAX
Adelaide, South Australia, Australia, 5000
Sponsors and Collaborators
BeiGene
Investigators
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Study Director: William Novotony, MD Beigne
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Responsible Party: BeiGene
ClinicalTrials.gov Identifier: NCT04163523    
Other Study ID Numbers: BGB-3111-103
First Posted: November 14, 2019    Key Record Dates
Last Update Posted: November 14, 2019
Last Verified: November 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by BeiGene:
Phase 1, pharmacokinetics safety
Additional relevant MeSH terms:
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Zanubrutinib
Antineoplastic Agents
Protein Kinase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action