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- Ensaio Clínico NCT07857837
Study of Sulthiame (S-054502) in Participants With Renal Impairment and Matched Healthy Controls
A Phase 1, Multi-center, Open-label, Parallel-group Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Sulthiame (S-054502) in Participants With Varying Degrees of Renal Impairment and Matched Healthy Control Participants With Normal Renal Function
The purpose of this study is to evaluate the pharmacokinetics (PK), safety, and tolerability of sulthiame in participants with mild and moderate renal impairment compared to those in healthy participants with normal renal function.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 1
Contactos e Locais
Contato de estudo
- Nome: Shionogi Clinical Trials Administrator Clinical Support Help Line
- Número de telefone: 1-800-849-9707
- E-mail: Shionogiclintrials-admin@shionogi.co.jp
Locais de estudo
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Florida
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Altamonte Springs, Florida, Estados Unidos, 32714
- Omega Research Orlando, LLC
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Miami Lakes, Florida, Estados Unidos, 33016
- Floridian Clinical Research
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Key Inclusion Criteria:
All Participants:
- Participants who are considered to be healthy (for normal renal function participants) or medically stable (for participants with renal impairment), as determined by medical evaluation including previous medical conditions/concurrent medical conditions, physical examination, clinical laboratory tests, vital sign measurements, and 12-lead electrocardiography (ECG) during the screening period and on Day -1. Participants with renal impairment should have no clinically significant changes (based on investigator clinical judgment) in previous medical conditions/concurrent medical conditions or laboratory values within 3 months prior to administration of the investigational intervention on Day 1.
- Body weight ≥ 60 kilograms (kg) for male and ≥ 50 kg for female and body mass index (BMI) within the range 18.5 to 40.0 (inclusive) kg/square meter (m^2) .
Participants With Renal Impairment (Groups A and B):
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Participants who have mild and moderate renal impairment based on estimated glomerular filtration rate (eGFR) calculated using the 2021 Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) creatinine formula and the participant's body surface area (BSA) at the screening visit (Day -28 to -2).
- Mild renal impairment: 60 to < 90 milliliters (mL)/minute (min)
- Moderate renal impairment: 30 to < 60 mL/min
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A stable medication regimen is required, defined as not starting new drug(s) or changing dosage(s) within 14 days prior to administration of the investigational intervention through the follow-up/early termination visit.
Healthy Participants With Normal Renal Function (Group C):
- Participants with clinical laboratory tests within normal reference range for the laboratory, or abnormal but considered not clinically significant by the investigator. Renal function based on eGFR, calculated based on the 2021 CKD EPI creatinine formula and the participant's BSA, must be normal (eGFR ≥ 90 mL/min) at the screening visit.
- Matched to an individual participant with moderate renal impairment (Group B) with respect to age (± 10 years), body weight (± 10 kg), and sex.
Key Exclusion Criteria:
All Participants:
- History or presence of/significant history of or current cardiovascular, respiratory, hepatic, gastrointestinal (GI), endocrinological, hematological, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking the investigational intervention; or interfering with the interpretation of data.
- History of GI surgery such as gastrectomy and enterectomy that could lead to clinically significant gastrointestinal dysfunction.
- Current or chronic history of liver disease or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
- Participants with fluctuating or rapidly deteriorating renal function.
- Participation in any other clinical study or any other type of medical research involving administration of an investigational intervention (new chemical entity) within 28 days or 5 half-lives of the investigational intervention (if known) prior to dosing, whichever is longer.
Participants With Renal Impairment (Groups A and B):
- Participant with clinically significant laboratory values in the opinion of the investigator or outside the protocol-defined ranges or limits during the screening period or on Day -1.
Healthy Participants With Normal Renal Function (Group C):
- History or presence of/significant history of or current renal disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking the investigational intervention; or interfering with the interpretation of data.
Note: Other protocol-defined inclusion and exclusion criteria may apply.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Não randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Group A: Participants with Mild Renal Impairment
Participants with mild renal impairment will receive a single dose of sulthiame in the fasted state on Day 1. |
Tablet for oral administration
Outros nomes:
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Experimental: Group B: Participants with Moderate Renal Impairment
Participants with moderate renal impairment will receive a single dose of sulthiame in the fasted state on Day 1. |
Tablet for oral administration
Outros nomes:
|
|
Experimental: Group C: Healthy Participants With Normal Renal Function
Healthy participants with normal renal function will receive a single dose of sulthiame in the fasted state on Day 1. |
Tablet for oral administration
Outros nomes:
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Prazo |
|---|---|
|
Maximum Observed Plasma Concentration (Cmax) of Sulthiame
Prazo: 0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
|
Time to Reach Cmax (Tmax) of Sulthiame
Prazo: 0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
|
Area Under the Plasma Concentration-time Curve Extrapolated From Time 0 to the time of the Last Quantifiable Concentration After Dosing (AUC0-last) of Sulthiame
Prazo: 0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
|
Cmax of Sulthiame Metabolite
Prazo: 0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
|
Tmax of Sulthiame Metabolite
Prazo: 0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
|
AUC0-last of Sulthiame Metabolite
Prazo: 0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
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Número de participantes com eventos adversos emergentes do tratamento (TEAES)
Prazo: Dia 1 até o dia 15
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Dia 1 até o dia 15
|
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
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- 2515A4313
Plano para dados de participantes individuais (IPD)
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Informações sobre medicamentos e dispositivos, documentos de estudo
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