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Pharmacokinetic and Safety Study of HYR-PB21 vs Bupivacaine Hydrochloric Acid in Healthy Participants

21 de agosto de 2026 atualizado por: Fruithy Holdings Limited

A Phase I, Randomized, Single-blind, Active-controlled, Parallel Study to Evaluate the Safety and Pharmacokinetics of Single-Dose HYR-PB21 Versus Bupivacaine Hydrochloric Acid for Subcutaneous Injection in Healthy Participants

This is a Phase I, randomized, single-blind, active-controlled, single-dose, parallel-group study to evaluate the safety and pharmacokinetic (PK) profile of HYR-PB21, a pamoate-formulated bupivacaine injectable, in healthy adult participants.

Participants are randomized to receive a single subcutaneous dose of HYR-PB21 at one of three dose levels (100 mg, 200 mg, or 400 mg) or a single 100 mg dose of Bupivacaine hydrochloride injection (as base) as active control.

The primary objectives are to characterize the PK profile of HYR-PB21 at the three dose levels compared with Bupivacaine hydrochloride, and to determine the Pharmacokinetics characteristics of the pamoic acid moiety following HYR-PB21 administration. Secondary objectives are to extend cumulative safety and tolerability observations of single subcutaneous doses of HYR-PB21 in healthy adults.

Visão geral do estudo

Descrição detalhada

Background and Rationale

HYR-PB21 for Injectable Suspension (HYR-PB21) is a novel long-acting formulation under investigation for local analgesia. Preclinical and clinical data supporting this investigational new drug include four previous Phase 1 or 2 studies conducted in Chinese participants and one Phase 1 study in Australian participants. These prior studies evaluated the pharmacokinetics (PK), pharmacodynamics, safety, and tolerability of HYR-PB21. The current study is designed to serve as a bridging study to extrapolate the existing ex-US PK and safety data to a North American population. Upon successful completion, the data from this study will be utilized to define the proposed Phase 3 efficacy dose or dose range for North American patients.

Study Design and Objectives

This is a Phase I, randomized, single-blind, active-controlled, single-dose, parallel-group study designed to evaluate the safety and pharmacokinetic profile of HYR-PB21 compared to Bupivacaine HCl Injection in healthy adult participants.

The primary objectives are:

To characterize and compare the plasma PK profile of three dose levels of HYR-PB21 (100 mg, 200 mg, and 400 mg) versus a single dose of 100 mg Bupivacaine hydrochloride Injection (calculated as base).

To determine the pharmacokinetic characteristics of the pamoic acid component following administration of HYR-PB21 at the aforementioned dose levels.

The secondary objective is to further evaluate the cumulative safety and tolerability of single subcutaneous doses of HYR-PB21 in healthy participants.

Participants and Interventions

A total of 28 healthy adult participants will be randomized in a 1:1:1:1 ratio into four parallel treatment arms (N=7 per arm).All treatments will be administered via subcutaneous injection.

Extensive blood sampling will be conducted to characterize the plasma concentration-time profiles. Sampling time points are: pre-dose (within 2 hours prior to dosing), 15 (±2) min, 30 (±2) min, 1 (±2) h, 2 (±3) h, 4 (±3) h, 8 (±5) h, 12 (±5) h, 18 (±5) h, 24 (±5) h, 30 (±5) h, 36 (±5) h, 48 (±5) h, 60 (±5) h, 72 (±5) h, 96 (±5) h, 120 (±5) h, and 144 (±5) h post-dose.

Safety and tolerability will be monitored throughout the study duration. Assessments include:

Treatment-emergent adverse events (TEAEs), including monitoring for Local Anesthetic Systemic Toxicity (LAST) and local injection site reactions, etc.

Tipo de estudo

Intervencional

Inscrição (Estimado)

28

Estágio

  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  1. Healthy male or female adult participants
  2. Age 18 to 50 years old (inclusive)
  3. Body mass index (BMI) of 18.0 to 32.0 kg/m2 and weight ≥50 kg.
  4. Participant is generally healthy, as determined by the Investigator based on medical history, physical examination, clinical laboratory test results, vital signs, and 12-lead electrocardiogram (ECG) at screening.

    Additional Detailed Inclusion Criteria Include:

  5. Female participants who engage in heterosexual intercourse must be non-pregnant or non-lactating. Female participants of childbearing potential must agree to use 2 acceptable methods of contraception with their male partner from screening until 6 months after the last dose of the study drug and refrain from donating ovum for this same period. (Refer to contraception section).Females of non-childbearing potential must either be :

    1. Post menopausal as defined by at least 12 months of consecutive Amenorrhea and Follicle-Stimulating Hormone(FSH) and estradiol confirming Post menopausal status at screening. See Appendix Section 13 for additional details.
    2. Surgically sterile at least 6 months prior to screening with documentation.
    1. Bilateral tubal ligation
    2. Hysterectomy (partial or total)
    3. Bilateral salpingectomy
    4. Bilateral oophorectomy
  6. Male participants, if sexually active with a female partner of child-bearing potential, must be vasectomized or agree to take appropriate precautions to prevent conception, including practicing an effective method of contraception, and must not donate sperm from screening through 12 weeks following administration of the last dose of study medication.
  7. Only non-smokers are eligible. For a period of at least six months prior to Screening, all participants must have been free from excessive alcohol intake or regular use of illegal recreational drugs. Participants with any past or current history of marijuana use are not eligible for the study.
  8. Ability to understand and willingness to sign a written informed consent form (The consent form must be signed by the participant prior to any study-specific procedures.)
  9. Willingness and able to comply with catheter placement and blood draws throughout the course of study and comply with study procedures and follow-up examination.

Exclusion Criteria:

Participants will be excluded if they have

  1. A history of hypersensitivity or idiosyncratic reactions to amide-type local anesthetics;
  2. Have a personal or family history of clotting disorder or hematologic abnormality, such as excessive bleeding, joint hematoma, thrombovascular disease, thrombocytopenia, or any chronic condition requiring treatment with transfusions; have a history of recurrent bleeding episodes (eg, epistaxis, bruising or gingival bleeding) within 1 month prior to Screening, or a longstanding history of such bleeding.
  3. Participants who were detected to have Glucose-6-phosphate dehydrogenase(G6PD) deficiency during the screening period.

    Additional detailed exclusion criteria include:

  4. Females who are pregnant, lactating, or have plans to become pregnant during the study
  5. History and/or recent evidence within six months prior to Screening of alcohol or drug/substance abuse disorder
  6. History of clinically significant allergies, including drug allergies, or allergic bronchial asthma, or related bronchospastic conditions
  7. Participants who have a history of unexplained syncope or fainting or a condition that predisposes them to syncope, such as hypotension, orthostatic hypotension, bradycardia, or dehydration.
  8. Participants who have used P-gp and/or Cytochrome P450 hepatic microsomal enzyme-inducing or inhibiting drugs (e.g., propafenone, voriconazole, fluconazole, cimetidine) within 30 days of first dosing, refer to Appendix 15-16 for detailed list
  9. Participants with a history or presence of significant cardiovascular, pulmonary, hepatic, gallbladder or biliary tract, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, psychiatric disease, or active sexually transmitted disease to include:

    1. Current or history of thrombosis or thromboembolic disorders
    2. Any history of malignancy, especially breast cancer or other hormone-sensitive cancers
    3. Undiagnosed abnormal vaginal bleeding unrelated to pregnancy
    4. Cholestatic jaundice of pregnancy
    5. Liver tumors, benign or malignant, or active liver disease
    6. Uncontrolled hypertension
  10. History or evidence of acute or chronic respiratory disorders, including but not limited to chronic obstructive pulmonary disease (COPD) or asthma
  11. History or presence of significant cardiovascular abnormalities, including, without limitation, severe bradycardia, sick sinus syndrome, second- or third-degree atrial ventricular block, long QT syndrome, cardiogenic shock, and decompensated heart failure
  12. Participant family history of sudden cardiac death or long QT syndrome and baseline QT prolongation >450 for males and >470 for females at screening
  13. Participants with estimated glomerular filtration rate (eGFR - utilizing Chronic Kidney Disease Epidemiology Collaboration formula) < 80 mL/min/1.73 m2; participants with slightly lower values may be included upon agreement between the sponsor medical representative and the Principal Investigator at screening
  14. Participants meeting any of the following laboratory criteria will be excluded:

    1. Screening total bilirubin > 1.3 mg/dL; participants with a documented history of Gilbert's syndrome can be enrolled if the direct bilirubin is < 0.4 mg/dL
    2. Screening alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP) > upper limits of normal (ULN)
    3. Screening platelets < 140,000/microliter
    4. Screening international normalized ratio > 1.2
  15. Participants who test positive at screening for human immunodeficiency virus (HIV), Hepatitis B surface antigen (HBsAg), or Hepatitis C virus (HCV) antibody
  16. Participants who test positive at Screening and/or admission (Day 0) for alcohol and/or drugs of abuse
  17. Participants who donated ≥ 500 mL of blood within 56 days prior to the study period or ≥ 50 mL and ≤ 499 mL of blood within 30 days prior to the study period
  18. Participants who are unable to refrain from or anticipatethe use of any medication, including prescription and non-prescription drugs or herbal remedies (such as St. John's Wort [Hypericum perforatum]) approximately 2 weeks prior to study drug administration.
  19. Participant who is unable to refrain from excessive alcohol consumption within one week prior to the study start throughout the study, until the final study visit. Moderate alcohol consumption is defined as one standard drink per day for women and two drinks per day for men; whereby one standard drink is equivalent to 12 oz beer (5% alcohol), 5 ounces of wine (12% alcohol), and 1.5 ounces of 80 proof (40% alcohol). Excessive consumption would be considered consistently in excess of twice the moderate recommendation.
  20. Participant who consumes excessive amounts of caffeine for one month prior to the study drug administration, defined as greater than six servings (one serving is approximately equivalent to 120 mg of caffeine) of coffee, tea, cola, or other caffeinated beverages per day
  21. Participants who donated plasma (e.g., plasmapheresis) within 14 days prior to the study period; participants will be advised not to donate plasma for 14 days after completing the study
  22. Participant with tattoos to the abdominal area, which in the opinion of the investigator, could interfere with study drug administration.
  23. Participant has poor venous access or has a history of difficulty tolerating venipuncture such as vasovagal syncope.
  24. Participants who have participated in another clinical trial which required blood draws within 30 days prior to the first study drug dosing
  25. Have any other condition that, in the opinion of the Investigator, would interfere with a participant's ability to adhere to the protocol, interfere with assessment of the investigational product, or compromise the safety of the participant or the quality of the data.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Ciência básica
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: HYR-PB21, 100 mg
HYR-PB21, 100 mg, administered as a single subcutaneous injection
HYR-PB21, 100 mg, administered as a single subcutaneous injection.
Outros nomes:
  • Bupivacaine Pamoic acid Injection, 100 mg
Experimental: HYR-PB21, 200 mg
HYR-PB21, 200 mg,administered as a single subcutaneous injection
HYR-PB21 200 mg, administered as a single subcutaneous injection.
Outros nomes:
  • Bupivacaine Pamoic acid Injection, 200 mg
Experimental: HYR-PB21, 400 mg
HYR-PB21, 400 mg, administered as a single subcutaneous injection
HYR-PB21 400 mg, administered as a single subcutaneous injection.
Outros nomes:
  • Bupivacaine Pamoic acid Injection, 400 mg
Comparador Ativo: Bupivacaine hydrochloride, 100 mg (as base)
Bupivacaine hydrochloride, 100 mg, administered as a single subcutaneous injection
Bupivacaine Hydrochloric acid injection 100 mg (expressed as bupivacaine base), administered as a single subcutaneous injection. Active comparator.
Outros nomes:
  • MARCAINE®, 100 mg

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Maximum observed plasma concentration(Cmax) of bupivacaine
Prazo: Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
The maximum observed plasma concentrations of bupivacaine was directly obtained from the observed concentration-time curves. Units: ng/mL. The PK parameters will be analyzed using the non-partial model. For ease of statistical comparison, the Cmax values will be log-transformed.
Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
Maximum observed plasma concentration(Cmax) of pamoic acid
Prazo: Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
The maximum observed plasma concentrations of pamoic acid was directly obtained from the observed concentration-time curves. Units: ng/mL. The PK parameters will be analyzed using the non-partial model. For ease of statistical comparison, the Cmax values will be log-transformed.
Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
Area Under the Curve(AUC0-t) of bupivacaine
Prazo: Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
During the period from time zero (the administration time) to Tlast (the last time point when the concentration reaches or exceeds the quantitative lower limit), the area under the plasma concentration-time curve of bupivacaine was calculated according to the mixed logarithmic linear trapezoidal rule. Unit: ng·hour/mL.
Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
Area Under the Curve(AUC0-t) of pamoic acid
Prazo: Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
During the period from time zero (the administration time) to Tlast (the last time point when the concentration reaches or exceeds the quantitative lower limit), the area under the plasma concentration-time curve of pamoic acid was calculated according to the mixed logarithmic linear trapezoidal rule. Unit: ng·hour/mL.
Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
Terminal elimination half-life(t1/2) of bupivacaine
Prazo: Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
The apparent terminal half-life of bupivacaine was calculated using the formula ln(2)/λz, where λz is the terminal elimination rate constant determined through linear regression of the logarithm of the final stage concentration (at least 3 data points, along with the R² value). The unit is hour.
Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
Terminal elimination half-life(t1/2) of pamoic acid
Prazo: Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
The apparent terminal half-life of pamoic acid was calculated using the formula ln(2)/λz, where λz is the terminal elimination rate constant determined through linear regression of the logarithm of the final stage concentration (at least 3 data points, along with the R² value). The unit is hour.
Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
Time of maximum observed plasma concentration(Tmax) of bupivacaine
Prazo: Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
The time at which bupivacaine reach their maximum plasma concentrations is recorded based on the actual sampling time corresponding to the Cmax value (if there are multiple identical Cmax values, the time of the first occurrence is taken as the reference). Unit: hour
Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
Time of maximum observed plasma concentration(Tmax) of pamoic acid
Prazo: Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose
The time at which pamoic acid reach their maximum plasma concentrations is recorded based on the actual sampling time corresponding to the Cmax value (if there are multiple identical Cmax values, the time of the first occurrence is taken as the reference). Unit: hour
Predose; 0.25, 0.5, 1, 2, 4, 8, 12, 18, 24, 30, 36, 48, 60, 72, 96, 120, 144, 168 hours and Day 14 post-dose

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Number of participants with abnormal laboratory tests results, abnormal vital signs,abnormal ECG readings, abnormal physical examination findings
Prazo: Baseline through Day 28 (or 30 days post-dose)
Laboratory tests include hematology (e.g., hemoglobin, white blood cell count, platelet count), blood chemistry (e.g., Alanine Aminotransferase, Aspartate Aminotransferase, total bilirubin, creatinine, glucose), urinalysis, and coagulation (e.g., Prothrombin Time, Activated Partial Thromboplastin Time). Vital signs include sitting systolic/diastolic blood pressure, pulse rate, respiratory rate, and body temperature. Abnormal is defined as a value outside the institutional reference range. Clinically significant abnormal values will also be summarized separately, defined as CTCAE Grade ≥1 . Values are summarized as number (%) of participants.
Baseline through Day 28 (or 30 days post-dose)

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Diretor de estudo: shanchun zhang, Doctor, Fruithy Holdings Limited

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de agosto de 2026

Conclusão Primária (Estimado)

1 de setembro de 2026

Conclusão do estudo (Estimado)

1 de outubro de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

10 de julho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

16 de julho de 2026

Primeira postagem (Real)

21 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

24 de agosto de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

21 de agosto de 2026

Última verificação

1 de agosto de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • HYR-PB21-US-01

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Sim

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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