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

Healthy Volunteers Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04163523
• Other study ID #: BGB-3111-103
• Status: Completed
• Phase: Phase 1
• Start date: May 25, 2016
• Est. completion date: July 21, 2016

Study information

• Verified date: November 2019
• Source: BeiGene
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 18
• Est. completion date: July 21, 2016
• Est. primary completion date: July 21, 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

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

Related Conditions & MeSH terms

• Healthy Volunteers

Intervention

Drug:
• Zanubrutinib

Locations

Country	Name	City	State
Australia	CMAX	Adelaide	South Australia

Sponsors (1)

Lead Sponsor	Collaborator
BeiGene

Country where clinical trial is conducted

Australia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pharmacokinetic Parameter: Plasma concentration of zanubrutinib as measured by area under concentration-time curve (AUC(0-24))		up to 24 hours
Primary	Pharmacokinetic Parameter: Plasma concentration of zanubrutinib as measured by area under concentration-time curve (AUC(0-8))		up to 2 months
Primary	Pharmacokinetic Parameter: Peak Plasma Concentration (Cmax) of zanubrutinib		up to 2 months
Primary	Pharmacokinetic Parameter: Time to Reach Peak Plasma Concentration (Tmax) of zanubrutinib		up to 2 months
Primary	Pharmacokinetic Parameter: Half-life Period of zanubrutinib (T1/2)		up to 2 months