Evaluate the Pharmacokinetics and Safety of EXPAREL® Following Subcutaneous Administration in Healthy Chinese Subjects

Healthy Subjects Clinical Trial

Official title:

A Phase 1, Open Label Study to Evaluate the Pharmacokinetics and Safety of EXPAREL® Following Subcutaneous Administration in Healthy Chinese Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04158102
• Other study ID #: NB-EXP-1001
• Status: Completed
• Phase: Phase 1
• Start date: November 7, 2019
• Est. completion date: December 26, 2019

Study information

• Verified date: November 2019
• Source: Nuance Pharma (shanghai) Co., Ltd
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a single-center, open-label, single-dose study to evaluate the safety, pharmacokinetics in healthy subjects

Description:

This is a phase I, open-label, single-dose in healthy subjects conducted at single center.The objectives are to evaluate the metabolic and safety profile of EXPAREL®. Each volunteer will receive one dose of the investigational drug via subcutaneous injection at multiple points during the study period. Study duration is around 54 days, including screening, confinement, ambulatory visit and a phone follow up.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: December 26, 2019
• Est. primary completion date: December 17, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Chinese male or female subjects, and his/her biological parents and grandparents are of Chinese ethnicity.

2. Aged =18 and =55 years of age at screening, inclusive.

3. Willing and able to give written informed consent and comply with the study visit schedule, study procedures and restrictions.

4. Generally, in good health with no clinically significant abnormalities as determined by medical history, physical examination, 12-lead ECG and clinical laboratory tests.

5. Have a body mass index (BMI) between 19.0 and 24.0 kg/m2, inclusive, and a body weight =50 kg at screening visit and baseline visit (Day -1).

Exclusion Criteria:

1. Female subjects who are pregnant (positive pregnancy result at screening and on Day -1), or lactating.

2. Female subjects of child bearing potential and sexually active don't agree to use medically acceptable contraceptive (e.g. insertable, injectable, transdermal, hormonal contraceptive) from the date of consent given until 30 days after administration of study drug. Menopausal woman don't have her menopausal status confirmed by follicle-stimulating hormone test at screening.

3. Male subjects who are sexually active don't agree to use condom plus spermicide since the dosing day till 90 days after administration of study drug.

4. Male subjects don't agree not to donate sperm since the dosing day till 90 days after administration of study drug.

5. Presence of any concomitant clinically significant diseases, that would interfere with the study based on the investigator's discretion.

6. History of hypersensitivity or idiopathic reaction to amide-type local anesthetics.

7. Has a positive urine drug screen result for drugs of abuse or a positive blood alcohol test at the Screening Visit or baseline visit (Day-1).

8. Has an abnormal (clinically significant) ECG at the screening visit. Entry of any subject with an abnormal (but not clinically significant) ECG must be approved and documented by signature of the Investigator or medically qualified subinvestigator.

9. Has a supine BP outside the ranges of 90 to 140 mmHg for systolic BP and 50 to 90 mmHg, inclusive, for diastolic BP, or resting pulse rate outside the range of 40 to 100 beats per minute. If any of the values are out of range, the assessment may be repeated twice for eligibility determination at the screening visit or baseline visit (Day-1).

10. Positive HIV test result at screening.

11. Positive testing for HBs Antigen and/or a positive Hepatitis C antibody test result at screening.

12. Has an abnormal laboratory values outside the reference range that are of clinical significance which may suggest of an underlying disease such as alanine aminotransferase (ALT) or aspartate aminotransferase (AST) values, greater than 1.5 times the upper limit of normal.

13. Intake prescription or over the counter products (vitamins, dietary supplements, herbal preparations, etc.) within 14 days or less than 5 half-lives (whichever is longer) prior to screening visit.

14. Blood loss or donation more than 450ml within 3 months prior to dosing.

15. Previous participation in an EXPAREL® study.

16. Administration of an investigational drug within 30 days or 5 elimination half-lives of the investigational drug, whichever is longer, prior to study drug administration, or planned administration of another investigational product or procedure during the subject's participation in this study.

Related Conditions & MeSH terms

• Healthy Subjects

Intervention

Drug:
• Bupivacaine liposome injectable suspension
Single dose of Bupivacaine liposome injectable suspension 266 mg in 20 mL

Locations

Country	Name	City	State
China	HUK Phase 1 clinical trials center	Hong Kong	Hongkong

Sponsors (1)

Lead Sponsor	Collaborator
Nuance Pharma (shanghai) Co., Ltd

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	plasma concentration	Maximum observed plasma concentration (Cmax)	up to 14 days
Primary	Area under the plasma concentration-versus-time curve	Area under the plasma concentration-versus-time curve from time 0 extrapolated to infinity after drug administration (AUC0-8)	up to 14 days
Secondary	Incidence of adverse events(AEs)which are related to exparel injection	Adverse events refer to any treatment related abnormality with clinical significance identified by means of vital signs examination, physical check-up, twelve leads electrocardiogram inspection and laboratory tests throughout the study. Adverse events reported by subjects would also be recorded in the entire trial. All these abnormal cases described above would be reported as incidence of adverse events.	up to 21 days