An Relative Bioavailability Study of BH006 for Injection in Healthy Subjects

Bioavailability Clinical Trial

Official title:

An Open-label, Randomized, Single-dose, Two-period Cross-over Study to Evaluate the Relative Bioavailability Between BH006 for Injection Per the Intended Dosage Regimen and Fosaprepitant and Palonosetron in Healthy Subjects

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06427681
• Other study ID #: BH006-BE-102
• Status: Not yet recruiting
• Phase: Early Phase 1
• Start date: May 2024
• Est. completion date: December 2024

Study information

• Verified date: May 2024
• Source: Zhuhai Beihai Biotech Co., Ltd
• Contact: Xiaohua Wei, PMD
• Phone: +86 13500248359
• Email: xhwei[@]bayhibiotech.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study is an open label, randomized, balanced, two period, two sequence, crossover, single dose, relative bioavailability study in healthy subjects.Each subject, meeting all the inclusion criteria and none of the exclusion criteria, will receive test product or reference product in a crossover manner based on randomization schedule. A balance between T-R and R-T randomization sequence will be ensured using statistical techniques. Blood samples for PK assessment will be collected prior to and after start of intravenous infusion on Day 1 (Period I), Day 15 (Period II).

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 40
• Est. completion date: December 2024
• Est. primary completion date: September 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Willing and able to provide signed and dated informed consent prior to any study-related procedures.

2. Willing and able to comply with all study procedures.

3. Subjects and their spouses must agree to use adequate contraception 14 days prior to the first dose, for the duration of study participation, and for 6 months following completion of therapy.

4. Healthy subjects of either gender, =18 years of age, or = 55 years of age.

5. Have a body weight (BW) of = 45.0 kg(female) / = 50.0 kg(male) and 18 = body mass index (BMI) = 28 kg/m2.

6. Subjects had normal vital signs (T: 35.9~37.6?; P: 50~100 beats/min; BP:

90~139mmHg/60~89mmHg, all including critical values) and good organ function prior to enrollment:

• 12-ECG: QTc <450 milliseconds for males and <470 milliseconds for females;

• Platelets = 100 × 109/L; neutrophil count = 1.5 × 109/L; hemoglobin = 110 g/L;

• Alanine aminotransferase, aspartate aminotransferase and bilirubin = ULN;

• Subjects with abnormal values on physical examination and the rest of the laboratory tests were also enrolled if the investigator determined that the abnormality was not clinically significant in the context of past medical history.

Exclusion Criteria:

1. Those who are known to be allergic to the investigational drug, its excipients, or similar drugs, or those who suffer from allergic diseases or belong to an allergic constitution (such as allergies to two or more drugs, food, or pollen).

2. Those who have a history of clinically serious disease and have not been cured, or those who currently have a disease that may significantly affect the PK or safety evaluation of the study drug.

3. Those with abnormal and clinically significant vital signs, 12-ECG, and clinical laboratory tests.

4. Major surgery within 90 days prior to study entry; minor surgery within 2 weeks prior to study entry.

5. Subjects who have received a vaccination within 30 days prior to the first dose.

6. Subjects who have used or using any drug within 30 days prior to the first dose that may have a significant impact on the PK or safety evaluation of this study drug, including, but not limited to, CYP3A4 inhibitors/agonists, drugs that may alter activity of drug metabolizing enzyme of liver.

7. Subjects who have participated in and used any clinical trial drug within 90 days prior to the first dose, or plan to participate in other clinical trials during this study.

8. Those with a history of alcohol abuse, or regular drinkers within 90 days prior to the first dose (14 units of alcohol per week: 1 unit = 285 mL of beer, or 25 mL of spirits, or 100 mL of wine), or those who could not abstain during the test, or had a positive alcohol breath test. (1 unit = 1 unit of alcohol = about 285 mL of beer or about 100 mL of red wine or about 25 mL of beverage containing 40% (v/v) alcohol).

9. Subjects who are addicted to tobacco (more than 5 cigarettes or equivalent per day) within 30 days prior to the first dose, or who were unable to quit smoking during the trial.

10. Subjects who have lost/donated more than 450 mL of blood (except physiological blood loss in females) within 90 days prior to the first dose, or who have received a blood transfusion or used a blood product, or who plan to donate blood during the trial or within 30 days of the end of the trial.

11. Subjects who have taken a special diet (including pitaya, mango, grapefruit, etc.) or have had strenuous exercise, or other factors affecting drug absorption, distribution, metabolism, or excretion within 14 days prior to the first dose.

12. Consumption of food or beverages containing alcoholic products or caffeine or xanthine within 48 hours before the first dose.

13. Subjects have a history of drug abuse within the past five years or a positive drug abuse screen.

14. Subjects have presence of Hepatitis B surface antigen (HBsAg) or a Positive Hepatitis C antibody test result, or positive human immunodeficiency virus (HIV) antibody test, or Positive test for syphilis spirochete antibodies at screening.

15. Female subjects who are pregnant or breastfeeding, or have a positive blood pregnancy test result at screening.

16. Subjects have other clinical significant findings within the 12 months prior to screening that indicate clinically significant disease of the following (including, but not limited to, gastrointestinal, renal, hepatic, neurological, haematological, endocrine, oncological, pulmonary, immunological, psychiatric, or cardiovascular disorders); and suffering from any condition that increases the risk of haemorrhage such as haemorrhoids, acute gastritis, or gastric and duodenal ulcers, intractable constipation.

17. Subjects who have a history of needle sickness, blood sickness or have a problem in collecting blood.

18. Subjects who have an acute illness or concomitant medication from the screening phase until the first dose.

19. Subjects who are engaged in high-altitude work, vehicle driving and other operators of machinery associated with danger.

20. Subjects have other issues that may lead to non-compliance or be unsuitable for inclusion by investigators' judgement.

Related Conditions & MeSH terms

• Bioavailability

Intervention

Drug:
• BH006 for injection
According to the random administration plan, the test product BH006 [(fosaprepitant and palonosetron) for injection] 150mg/0.25mg or the reference product [EMEND® (fosaprepitant) for injection 150 mg + Palonosetron hydrochloride injection 0.25 mg) were injected, and crossovered after a sufficient washing period (14 days), dosing is carried out for the second cycle study.
• Fosaprepitant for injection+Palonosetron hydrochloride injection
According to the random administration plan, the test product BH006 [(fosaprepitant and palonosetron) for injection] 150mg/0.25mg or the reference product [EMEND® (fosaprepitant) for injection 150 mg + Palonosetron hydrochloride injection 0.25 mg) were injected, and crossovered after a sufficient washing period (14 days), dosing is carried out for the second cycle study.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Zhuhai Beihai Biotech Co., Ltd

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Incidence of Adverse Events [Safety and Tolerability]	All adverse events (AE) defined by CTCAE version 5.0.	from the time of first study drug administration till end of study( Day24 Visit or Early Termination Visit)
Primary	Pharmacokinetic Analysis	The PK endpoints will be studied and assessed by PK parameters for aprepitant and palonosetron:Area Under the Curve From Time 0 Hours to Last Quantifiable Concentration(AUC0-t).	Period I&Period II:pre-dose to 168.000 hours after starting the infusion.
Primary	Pharmacokinetic Analysis	The PK endpoints will be studied and assessed by PK parameters for aprepitant and palonosetron:Area Under the Curve From Time 0 Hours to Infinity(AUC0-8).	Period I&Period II:pre-dose to 168.000 hours after starting the infusion.
Primary	Pharmacokinetic Analysis	The PK endpoints will be studied and assessed by PK parameters for aprepitant :Maximum Concentration (Cmax).	Period I&Period II:pre-dose to 168.000 hours after starting the infusion.
Secondary	Pharmacokinetic Analysis	For aprepitant, aprepitant and palonosetron : Apparent Terminal Elimination Half-Life (t1/2).	Period I&Period II:pre-dose to 168.000 hours after starting the infusion.
Secondary	Pharmacokinetic Analysis	For aprepitant, aprepitant and palonosetron : Time to Cmax (Tmax).	Period I&Period II:pre-dose to 168.000 hours after starting the infusion.