Pharmacokinetic Study of Single and Multiple Intravenous Administration of Nalbuphine Hydrochloride Injection in Healthy Chinese Volunteers

NCT06902103 | Completed Phase 1

• 1 other identifier: YZJ-NBF-PK-2302
• Study Type: interventional
• Target: 22
• Locations: 1 country
• Sites: 1

Brief Summary

Objective：To evaluate the pharmacokinetic characteristics and safety of single and multiple intravenous injections of nalbuphine hydrochloride injection in healthy subjects.

Conditions

Pain

Outcome Measures

Primary Outcomes (9)

• Cmax (Maximum drug plasma concentration)

  up to 12 hours after first administration

• AUC0-t (Total area under the plasma drug concentration-time curve from time of administration to the time of the last quantifiable drug concentration)

  up to 12 hours after first administration

• AUC0-∞ (Total area under the plasma drug concentration-time curve)

  up to 12 hours after first administration

• Tmax (Time to achieve Cmax)

  up to 12 hours after first administration

• T1/2z (Apparent terminal elimination half-life)

  up to 12 hours after first administration

• AUC_%Extrap (The percentage of the portion estimated through extrapolation)

  up to 12 hours after first administration

• MRT (Mean residence time)

  up to 12 hours after first administration

• CLz (Clearance of the analyte in plasma)

  up to 12 hours after first administration

• Occurence of adverse events

  up to 5 days for part A, up to 7 days for part B

Study Arms (2)

Group A

EXPERIMENTAL

Drug: Nabufine Hydrochloride Injection

Group B

EXPERIMENTAL

Drug: Nabufine Hydrochloride Injection

Interventions

Nabufine Hydrochloride Injection DRUG

PartA: Nabufine Hydrochloride Injection are administered Intravenous injection single dose

Group A

Eligibility Criteria

• Age: 18 Years - 45 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Subjects aged 18 \~ 65 years (inclusive, calculated from the date of signing the informed consent), half males and half females.
• Weight ≥ 50.0 kg for males, or ≥ 45.0 kg for females, and body mass index (BMI) in the range of 19.0 \~ 26.0 kg/m2 (inclusive), BMI= weight (kg)/height2(m2).
• Subjects have no plans to donate sperm or eggs, no plans to become pregnant and voluntarily take effective contraceptive measures (including partners) from signing the informed consent form to 3 months after the last dose of investigational product. See Appendix 2 of the protocol for specific contraceptive measures.
• Subjects who are able to understand and willing to complete the study in strict compliance with the clinical protocol and sign the informed consent form.

You may not qualify if:

• Subjects with any history of clinically significant diseases or conditions that may affect the test results in the opinion of the investigator, including but not limited to the respiratory system (such as obstructive sleep apnea syndrome, chronic bronchial asthma, etc.), cardiovascular system (such as syncope, etc.), digestive system, endocrine system, nervous system (such as epilepsy), urinary system or blood, immune, mental and metabolic disease history.
• Subjects with a history of frequent nausea or vomiting of any etiology.
• Subjects with known history of drug, food or other substance allergy.
• Subjects who have poor peripheral venous access or have a history of needle and blood fainting.
• Pregnant or lactating women, or subjects with positive blood pregnancy test results.
• Subjects with clinically significant abnormal ECG findings at screening, such as QTcF ≥ 450 ms in men, QTcF ≥ 470 ms or PR interval ≥ 200 ms or QRS complex duration ≥ 120 ms in women.
• Subjects with abnormal vital signs at screening (systolic blood pressure \< 90 mmHg or \> 140 mmHg, diastolic blood pressure \< 50 mmHg or \> 90 mmHg; pulse \< 50 beats/min or \> 100 beats/min) or physical examination, laboratory tests (blood routine, urine routine, blood biochemistry, coagulation function), chest anteroposterior abnormal subjects with clinical significance (based on the judgment of clinicians).
• Those who are positive in any index screening of hepatitis B virus surface antigen, Treponema pallidum-specific antibody, human immunodeficiency virus antibody, or hepatitis C virus antibody at screening.
• Subjects with positive urine drug screening or any history of drug abuse within 1 year prior to screening.
• Subjects who frequently consume alcohol within 6 months prior to screening, i.e., consuming more than 14 units of alcohol per week (1 unit = 360 mL of beer or 45 mL of 40% spirits, alcohol or 150 mL of wine), or whose alcohol breath test result \> 0.0 mg/100 mL, or take any alcohol-containing products within 48 hours before the first use of investigational products, or who cannot stop using any alcohol products during the study.
• Subjects smoke an average of 5 or more cigarettes per day within 3 months prior to screening, or who have used tobacco products within 48 hours before the first use of investigational products, or those who cannot stop using any tobacco products during the study.
• Subjects who have donated blood or experienced massive blood loss (\> 400 mL, excluding blood loss during menstruation in women), received blood transfusions or used blood products within 3 months prior to screening.
• Subjects who participated in any clinical trial and administered investigational drugs or investigational medical devices within 3 months prior to screening.
• Subjects who have undergone surgical procedures within 4 weeks prior to screening, or plan to undergo surgical procedures during the study period.
• Subjects who have received attenuated/DNA nucleic acid/recombinant protein vaccination within 4 weeks before screening, or inactivated vaccination within 2 weeks before screening, or plan to receive any vaccination during the study period.

Sponsors & Collaborators

• Yangtze River Pharmaceutical Group Jiangsu Zilong Pharmaceutical Co. Ltd: lead

Study Sites (1)

The Third Xiangya Hospital of Central South University

Changsha, China

Location

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Purpose: BASIC SCIENCE
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 24, 2025
• First Posted: March 30, 2025
• Study Start: December 20, 2023
• Primary Completion: December 26, 2023
• Study Completion: January 18, 2024
• Last Updated: March 30, 2025

Record last verified: 2025-03

Locations

CN (1)