- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07615985
A Study to Test the Safety and Blood Levels of PMG1016 in Healthy Adults
A Phase 1a, First-in-human, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of PMG1016 in Healthy Volunteers
This study is a first-in-human (FIH), randomized, double-blind, placebo-controlled study of PMG1016 in healthy adult participants. It aims to investigate the safety, tolerability, PK, and immunogenicity of PMG1016 administered via IV infusion.
Cohort 1: Healthy participants receiving single doses of PMG1016 Dose 1 or placebo.
Cohort 2: Healthy participants receiving single doses of PMG1016 Dose 2 or placebo.
Cohort 3: Healthy participants receiving single doses of PMG1016 Dose 3 or placebo.
Cohort 4: Healthy participants receiving single doses of PMG1016 Dose 4 or placebo.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 1
Contactos e Locais
Contato de estudo
- Nome: Yaohui Wang
- Número de telefone: +86 13810669548
- E-mail: yaohui_wang@pulmongene.com
Locais de estudo
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Queensland
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Brisbane, Queensland, Austrália, 4006
- Nucleus Network (Brisbane)
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Contato:
- Richard Friend, Dr
- Número de telefone: (07) 3707 2720
- E-mail: r.friend@nucleusnetwork.com.au
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-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- Participants must be in good health based on medical history, physical exam, vital signs, ECG, and lab results at screening, as judged by the PI.
- BMI 17.5-32.0 kg/m² and body weight 50-100 kg for males or 45-100 kg for females
- No clinically significant lab abnormalities (hematology, coagulation, biochemistry, urinalysis) per PI discretion
- Females: Must be non-pregnant, non-lactating, and use double contraception (condom + hormonal method/vaginal ring/IUD) through study completion, unless surgically sterile, postmenopausal, or in same-sex relationships. Negative pregnancy tests required. No oocyte donation for 90 days post dose.
- Males: Must be surgically sterile, abstinent, or use condoms plus a highly effective method for female partners. Vasectomized males without proof of azoospermia must use condoms with WOCBP partners. No sperm donation for 90 days post dose.
Exclusion Criteria:
- History or evidence of any clinically significant medical condition (e.g., cardiovascular, gastrointestinal, endocrine, hematologic, psychiatric, renal, musculoskeletal, infectious, neurological, or other major disease) as determined by the PI.
- A PR <40 or >100 bpm or mean SBP >140 mmHg or DBP >95 mmHg (based on triplicate supine measurements after 5 minutes' rest).
- Mean QTcF >450 ms (males) or >470 ms (females) at Screening; one repeat triplicate ECG allowed at PI discretion
- Any clinically significant ECG abnormalities (rhythm, conduction, morphology) that may affect QTc interpretation, per PI judgment
- ALT, AST, or creatinine >1.5 × ULN, or total bilirubin or lymphocytes > ULN.
- Hemoglobin (HGB) below the lower limit of the normal range (ULN) prior to enrollment.
- Participants with a positive toxicology screening panel or positive alcohol breath test at Screening and on Day -1.
- Regular alcohol consumption defined as > 21 alcohol units per week. Participant is unwilling to abstain from alcohol beginning 48 hours prior to admission to the CRU and while residing at the CRU.
- Blood donation or significant blood loss (≥500 mL) within 60 days prior to the first IP administration.
- Plasma donation within 7 days prior to the first IP administration.
- Use of any investigational product/device within 30 days or 5 half-lives (whichever is longer), or participation in >4 investigational drug studies in the past year.
- Pregnant or lactating at Screening or planning pregnancy (self or partner) during the study or follow-up.
- Fever >37.5°C or symptomatic infection within 2 weeks before Screening; any infection requiring systemic antibiotics within 3 months; history of recurrent infections; or a positive SARS-CoV-2 PCR before CRU admission.
- Active malignancy, history of malignancy, or untreated precancerous lesions. Adequately treated or fully excised precancerous lesions are allowed.
- Participants with a known history of retinal diseases, including conditions such as prior retinal detachment.
- Participants with a history of recurrent epistaxis or gingival bleeding.
- Use of prescription medications (except hormonal contraception) within 2 weeks before dosing; mAb products within 5 half-lives; or OTC drugs, supplements, or herbal products within 7 days before dosing.
- History of anaphylaxis or severe allergy per PI judgment; mild untreated hay fever may be allowed.
- History of allergic reaction or hypersensitivity to any of the excipients in the IP.
- Positive screening test for HIV-1/2, HBsAg, HCV antibody, or syphilis.
- Any condition that, in the PI's judgment, may pose a risk to the participant or the study.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição sequencial
- Mascaramento: Dobro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Coorte 1
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Participants will be administered PMG1016 Dose 1 or placebo in a 100 mL IV infusion volume
Outros nomes:
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Experimental: Coorte 2
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Participants will be administered PMG1016 Dose 2 or placebo in a 100 mL IV infusion volume
Outros nomes:
|
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Experimental: Coorte 3
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Participants will be administered PMG1016 dose 3 or placebo in a 100 mL IV infusion volume
Outros nomes:
|
|
Experimental: Coorte 4
|
Participants will be administered PMG1016 dose 4 or placebo in a 100 mL IV infusion volume
Outros nomes:
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Treatment-emergent adverse events (TEAEs)
Prazo: Day 1 to Day 57
|
The incidence and severity occurred
|
Day 1 to Day 57
|
|
Serious adverse events (SAEs)
Prazo: From Day 1 to Day 57
|
The incidence and severity occurred
|
From Day 1 to Day 57
|
|
Number of participants with abnormal pulse rate
Prazo: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of participants with abnormal blood pressure
Prazo: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of participants with abnormal respiratory rate
Prazo: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of participants with abnormal tympanic temperature
Prazo: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal PR Interval
Prazo: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal QRS Duration
Prazo: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal QT interval
Prazo: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal RR interval
Prazo: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Valvular Abnormalities
Prazo: Day 1 to Day 29
|
The number of participants with clinically significant valvular abnormalities identified by transthoracic echocardiography (TTE)
|
Day 1 to Day 29
|
|
Number of Participants with Clinically Significant Abnormal Left Ventricular Ejection Fraction
Prazo: Day 1 to Day 29
|
The number of participants with clinically significant abnormalities in left ventricular ejection fraction (LVEF) assessed by transthoracic echocardiography (TTE)
|
Day 1 to Day 29
|
|
Number of Participants with Clinically Significant Abnormal Hematology Results
Prazo: Day 1 to Day 57
|
Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal Clinical Chemistry Results
Prazo: Day 1 to Day 57
|
Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal Urinalysis Results
Prazo: Day 1 to Day 57
|
Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal Physical Examination Findings
Prazo: Day 1 to Day 57
|
assessment of general appearance; head; ears; eyes; nose; throat; dentition; thyroid; chest (heart and lungs); abdomen; skin; neurological system; extremities; back; neck; musculoskeletal system; and lymph nodes
|
Day 1 to Day 57
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Incidence of anti-drug antibodies (ADA)
Prazo: From Day 1 to Day 57
|
Percentage of PMG1016-induced ADA positive participants and percentage of PMG1016-boosted ADA positive participants
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From Day 1 to Day 57
|
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Maximum serum PMG1016 concentration (Cmax)
Prazo: Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 Cmax in Serum
|
Varying timepoints through end of treatment, up to Day 57
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Time to maximum concentration (Tmax)
Prazo: Varying timepoints through end of treatment, up to Day 57
|
Determine PMG1016 Tmax in Serum.
|
Varying timepoints through end of treatment, up to Day 57
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Area under the serum drug concentration-time curve (AUC) from time zero to the last time point with measurable concentration (AUC0-t)
Prazo: Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 AUC and AUC0-t in Serum.
|
Varying timepoints through end of treatment, up to Day 57
|
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AUC from time zero to infinity (AUC0-∞)
Prazo: Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 AUC0-∞ in Serum.
|
Varying timepoints through end of treatment, up to Day 57
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The extrapolated portion of AUC0-∞ from Tlast to infinity (%AUCextrap)
Prazo: Varying timepoints through end of treatment, up to Day 57
|
Determine PMG1016 %AUCextrap in Serum.
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Varying timepoints through end of treatment, up to Day 57
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Terminal elimination half-life (t1/2)
Prazo: Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 t1/2 in Serum.
|
Varying timepoints through end of treatment, up to Day 57
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Apparent total body clearance (CL)
Prazo: Varying timepoints through end of treatment, up to Day 57
|
Determine PMG1016 CL in Serum.
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Varying timepoints through end of treatment, up to Day 57
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Apparent volume of distribution during the terminal phase (Vz)
Prazo: Varying timepoints through end of treatment, up to Day 57
|
Determine PMG1016 Vz in Serum.
|
Varying timepoints through end of treatment, up to Day 57
|
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Apparent terminal elimination rate constant (λz)
Prazo: Varying timepoints through end of treatment, up to Day 57
|
Determine PMG1016 λz in Serum.
|
Varying timepoints through end of treatment, up to Day 57
|
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
- Doenças urogenitais
- Processos Patológicos
- Doenças Urogenitais Masculinas
- Doenças renais
- Doenças Urológicas
- Doenças Urogenitais Femininas
- Doenças urogenitais femininas e complicações na gravidez
- Doença crônica
- Atributos da doença
- Insuficiência renal
- Condições Patológicas, Sinais e Sintomas
- Insuficiência Renal Crônica
Outros números de identificação do estudo
- PMG1016-1031
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
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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-
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-
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-
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