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- Ensaio Clínico NCT07585383
A Phase I Clinical Trial to Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of KR23248 Capsules in Healthy Adult Subjects
A Randomized, Double-blind, Placebo-controlled, Dose-escalating Phase I Clinical Trial to Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of Single and Multiple Doses of KR23248 Capsules in Healthy Adult Subjects
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
This study is a randomized, double-blind, placebo-controlled, dose-escalating Phase I trial, aiming to evaluate the safety, tolerability, and pharmacokinetic (PK) profiles of single and multiple oral doses of KR23248 capsules in healthy adult subjects. The study consists of two parts: Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) studies.
The single ascending dose study plans to enroll 54 healthy subjects, with predefined dose escalation levels of 0.5 mg, 1.0 mg, 2.0 mg, 3.0 mg, 4.5 mg, and 6.0 mg in sequence. The multiple ascending dose study sets the initial dose at 2.0 mg, with 12 healthy subjects planned for enrollment.
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 1
Contactos e Locais
Contato de estudo
- Nome: Huafang Li
- Número de telefone: +8618017311256
- E-mail: lhlh_5@163.com
Estude backup de contato
- Nome: Yan Li
- Número de telefone: +8613046600636
- E-mail: liyan7721@163.com
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- Healthy male/female subjects aged ≥ 18 years and ≤ 45 years (inclusive) at the time of signing the informed consent form.
- Body Mass Index (BMI) ranging from 18.5 to 28.0 kg/m² (inclusive) at screening; male subjects with body weight ≥50 kg and female subjects with body weight ≥45 kg.
- Subjects who voluntarily participate in the trial and sign the informed consent form after understanding the purpose, content, procedures, and potential risks of the trial.
- Subjects who can communicate well with the investigators, are willing and able to comply with lifestyle restrictions specified in the protocol, and cooperate with study procedures.
Exclusion Criteria:
- Subjects with any diseases or dysfunctions in present illness and medical history that may interfere with the clinical trial, including but not limited to neurological and psychiatric diseases, cardiovascular diseases (e.g., congenital long QT syndrome), urinary system disorders, digestive system disorders, respiratory system disorders, musculoskeletal system disorders, metabolic and endocrine system disorders, skin diseases, hematological diseases, immune system diseases, and tumors.
- Subjects with any surgical condition or medical history that may significantly affect drug absorption, distribution, metabolism and excretion, or may pose a risk to the subject participating in the trial; such as a history of gastrointestinal surgery (gastrectomy, gastroenterostomy, enterectomy, etc.), urinary tract obstruction or dysuria, gastroenteritis, peptic ulcer, and history of gastrointestinal bleeding.
- Subjects with a history of severe allergic reactions or known hypersensitivity to any ingredients of the investigational product.
- Subjects with current or previous psychiatric disorders or cerebral dysfunction; those assessed to be at suicide risk based on the Columbia-Suicide Severity Rating Scale (C-SSRS), or by the investigator's clinical assessment, or those with a history of self-harm behavior.
- Subjects with a history of substance abuse within 1 year prior to administration or with a positive urine drug screening result.
- Subjects with a history of alcohol abuse within 6 months prior to screening (i.e., more than 14 standard units per week; 1 standard unit = 360 mL beer, or 45 mL spirits with 40% alcohol content, or 150 mL wine); or with a positive breath alcohol test; or unwilling to abstain from alcohol and any alcohol-containing products from screening until the last PK blood collection.
- Subjects with a history of surgery within 3 months prior to screening, or who have not recovered from surgery, or have a planned surgery scheduled during the trial.
- Subjects who have donated blood or experienced blood loss ≥ 400 mL within 3 months prior to screening, or ≥ 200 mL within one month, or have a history of blood product transfusion.
- Subjects who have participated in any clinical trial and received investigational drugs or medical devices within 3 months prior to screening.
- Subjects who have received vaccination within 30 days prior to screening, or have a vaccination plan during the entire study period.
- Subjects who have taken any medications within 28 days or 5 half-lives (whichever is longer) prior to screening and during the entire study period, including prescription drugs, over-the-counter drugs, herbal medicines, and any drugs that inhibit or induce hepatic drug-metabolizing enzymes (e.g., inducers and/or inhibitors of CYP3A4, CYP2D6, and CYP3A5).
- Female subjects who are pregnant, breastfeeding, or have a positive pregnancy test; or those who refuse to adopt effective non-pharmacological contraceptive measures (e.g., abstinence, intrauterine device, condoms with vaginal spermicide) throughout the study period and within 28 days after the end of administration; or those with a plan to donate sperm or ova.
- Subjects with clinically significant abnormal findings judged by the investigator in comprehensive physical examination, vital signs, laboratory tests and 12-lead electrocardiogram; including but not limited to: QTc > 450 ms in males and > 470 ms in females (Fridericia correction); resting pulse rate < 55 beats/min or > 100 beats/min; systolic blood pressure < 90 mmHg or ≥ 140 mmHg; diastolic blood pressure < 60 mmHg or ≥ 90 mmHg.
- Subjects with non-negative results for Hepatitis B surface antigen (HBsAg), Hepatitis C antibody (HCV-Ab), Human Immunodeficiency Virus antibody (HIV-Ab), and Toluidine Red Untreated Serum Test (TRUST).
- Subjects with alanine transaminase (ALT), creatinine (Cr) or serum prolactin level exceeding 2 times the upper limit of normal during the screening period.
- Subjects who smoke an average of ≥ 5 cigarettes per day within 3 months prior to screening, or are unable to abstain from any tobacco products during the trial.
- Subjects with an average daily intake of ≥ 5 cups of coffee or tea (200 mL per cup) within 3 months prior to screening, or are unable to discontinue intake during the trial.
- Subjects with special dietary requirements who cannot follow a unified study diet, or have difficulty in swallowing.
- Subjects who have consumed food or beverages containing grapefruit and/or pomelo within 7 days prior to administration.
- Subjects who have consumed xanthine-rich food or beverages (e.g., tea, coffee, cola, chocolate) within 3 days prior to administration.
- Subjects with poor compliance or other conditions deemed unsuitable for participation in the trial by the investigator.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Dobro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Part 1 cohort 1
SAD Cohort 1: single oral dose of 0.5mg KR23248 capsule
|
Participants will recieve a single oral dose of KR23248
Outros nomes:
|
|
Experimental: Part 1 cohort 2
SAD Cohort 2: single oral dose of 1.0mg KR23248 capsule
|
Participants will recieve a single oral dose of KR23248
Outros nomes:
|
|
Experimental: Part 1 cohort 3
SAD Cohort 3: single oral dose of 2.0mg KR23248 capsule
|
Participants will recieve a single oral dose of KR23248
Outros nomes:
|
|
Experimental: Part 1 cohort 4
SAD Cohort 4: single oral dose of 3.0mg KR23248 capsule
|
Participants will recieve a single oral dose of KR23248
Outros nomes:
|
|
Experimental: Part 1 cohort 5
SAD Cohort 5: single oral dose of 4.5mg KR23248 capsule
|
Participants will recieve a single oral dose of KR23248
Outros nomes:
|
|
Experimental: Part 1 cohort 6
SAD Cohort 6: single oral dose of 6.0mg KR23248 capsule
|
Participants will recieve a single oral dose of KR23248
Outros nomes:
|
|
Comparador de Placebo: Part 1 cohort 7
SAD cohort 7: single oral dose of placebo capsule
|
Os participantes receberão placebo
Outros nomes:
|
|
Experimental: Part 2 KR23248 2.0mg
MAD: Multiple oral doses of 2.0mg KR23248 capsules administered once daily for 14 consecutive days
|
Participants will recieve a single oral dose of KR23248
Outros nomes:
|
|
Comparador de Placebo: Part 2 Placebo
MAD: Multiple oral doses of placebo capsules administered once daily for 14 consecutive days
|
Os participantes receberão placebo
Outros nomes:
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Incidence of adverse events (AEs), serious adverse events(SAEs), drug-related AEs, and AEs leading to study withdrawal
Prazo: SAD:Day 1 to Day14 MAD:Day1 to Day28
|
The number and percentage of participants with AEs,SAEs, drug-related AEs, and AEs leading to study withdrawal will be determined
|
SAD:Day 1 to Day14 MAD:Day1 to Day28
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Cmax
Prazo: SAD:Day 1 to Day14 MAD:Day1 to Day28
|
Maximum Serum Concentration
|
SAD:Day 1 to Day14 MAD:Day1 to Day28
|
|
Tmax
Prazo: SAD:Day 1 to Day14 MAD:Day1 to Day28
|
Time to Reach the Maximum Serum Concentration
|
SAD:Day 1 to Day14 MAD:Day1 to Day28
|
|
t1/2
Prazo: SAD:Day 1 to Day14 MAD:Day1 to Day28
|
Elimination half-life
|
SAD:Day 1 to Day14 MAD:Day1 to Day28
|
|
λz
Prazo: SAD:Day 1 to Day14 MAD:Day1 to Day28
|
Terminal rate constant
|
SAD:Day 1 to Day14 MAD:Day1 to Day28
|
|
AUC0-t
Prazo: SAD:Day 1 to Day14 MAD:Day1 to Day28
|
Area under the plasma concentration-time curve from time zero to the last quantifiable concentration
|
SAD:Day 1 to Day14 MAD:Day1 to Day28
|
|
AUC0-∞
Prazo: SAD:Day 1 to Day14 MAD:Day1 to Day28
|
Area under the plasma concentration-time curve from time zero extrapolated to infinity
|
SAD:Day 1 to Day14 MAD:Day1 to Day28
|
|
CL/F
Prazo: SAD:Day 1 to Day14 MAD:Day1 to Day28
|
Apparent Clearance
|
SAD:Day 1 to Day14 MAD:Day1 to Day28
|
|
Vd/F
Prazo: SAD:Day 1 to Day14 MAD:Day1 to Day28
|
Apparent Volume of Distribution
|
SAD:Day 1 to Day14 MAD:Day1 to Day28
|
|
MRT
Prazo: SAD: Day1 to D14 MAD:Day1 to Day28
|
Mean residence time
|
SAD: Day1 to D14 MAD:Day1 to Day28
|
|
Css_min
Prazo: MAD:Day1 to Day28
|
Steady-state trough concentration
|
MAD:Day1 to Day28
|
|
Css_max
Prazo: MAD:Day1 to Day28
|
Steady-state peak concentration
|
MAD:Day1 to Day28
|
|
Tss,max
Prazo: MAD:Day1 to Day28
|
Time to Reach Maximum Concentration at Steady State
|
MAD:Day1 to Day28
|
|
Cavg,ss
Prazo: MAD:Day1 to Day28
|
Average Steady-State Concentration
|
MAD:Day1 to Day28
|
|
DF
Prazo: MAD:Day1 to Day28
|
Fluctuation Percentage
|
MAD:Day1 to Day28
|
|
Rac
Prazo: MAD:Day1 to Day28
|
Accumulation Factor
|
MAD:Day1 to Day28
|
|
AUCss
Prazo: MAD:Day1 to Day28
|
Area under the plasma concentration-time curve over a dosing interval at steady state
|
MAD:Day1 to Day28
|
Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- KR23248-202509
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
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