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- Ensaio Clínico NCT02171806
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Study of BI 1744 CL in Healthy Male and Female Volunteers
20 de junho de 2014 atualizado por: Boehringer Ingelheim
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Rising Inhalative Doses (2.5 μg, 10 μg, and 30 μg) of BI 1744 CL for 14 Days in Healthy Male and Female Volunteers (Doubleblind, Randomised, Placebo Controlled [at Each Dose Level] Study)
To investigate safety, tolerability, pharmacokinetics and pharmacodynamics of BI 1744 CL
Visão geral do estudo
Status
Concluído
Condições
Intervenção / Tratamento
Tipo de estudo
Intervencional
Inscrição (Real)
47
Estágio
- Fase 1
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
21 anos a 50 anos (Adulto)
Aceita Voluntários Saudáveis
Não
Gêneros Elegíveis para o Estudo
Tudo
Descrição
Inclusion Criteria:
- Healthy male or female based upon a complete medical history, including the physical examination, regarding vital signs (blood pressure (BP), pulse rate (PR)), 12-lead ECG measurement, and clinical laboratory tests. There is no finding deviating from normal and of clinical relevance. There is no evidence of a clinically relevant concomitant disease.
- Age ≥21 and ≤50 years
- BMI ≥18.5 and <30 kg/m2 (Body Mass Index)
- Signed and dated written informed consent prior to admission to the study in accordance with Good Clinical Practice and the local legislation
Exclusion Criteria:
- Any finding of the medical examination (including BP, PR, and ECG measurements) deviating from normal and of clinical relevance
- Evidence of a clinically relevant concomitant disease
- Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
- Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
- History of relevant orthostatic hypotension, fainting spells or blackouts
- Chronic or relevant acute infections
- History of relevant allergy/hypersensitivity (including allergy to the drug or its excipients) as judged clinically relevant by the investigator
- Intake of drugs with a long half-life (>24 hours) within at least 1 month or less than 10 half-lives of the respective drug prior to randomisation
- Use of drugs which might reasonably influence the results of the trial based on the knowledge at the time of protocol preparation within 10 days prior to randomisation
- Participation in another trial with an investigational drug within 2 months prior to randomisation
- Smoker (>10 cigarettes or >3 cigars or >3 pipes/day)
- Inability to refrain from smoking on trial days as judged by the investigator
- Alcohol abuse (more than 60 g alcohol a day)
- Drug abuse
- Blood donation (more than 100 mL blood within 4 weeks prior to randomisation or during the trial)
- Excessive physical activities within 1 week prior to randomisation or during the trial
- Any laboratory value outside the reference range that is of clinical relevance
- Inability to comply with dietary regimen of the study centre
The following exclusion criteria are specific for this study due to the known class side effect profile of ß2-mimetics:
- Asthma or history of pulmonary hyperreactivity
- Hyperthyrosis
- Allergic rhinitis in need of treatment
- Clinically relevant cardiac arrhythmia
- Paroxysmal tachycardia (>100 beats per minute).
For female subjects:
- Pregnancy
- Positive pregnancy test
- No adequate contraception e.g. oral contraception, sterilisation, IUD (intrauterine device). Females who are not surgically sterile will be asked to additionally use barrier contraception methods (e.g. condoms) prior to administration of study medication, during the study and at least 2 months after release from the study.
- Inability to maintain this adequate contraception during the whole study period
- Lactation period
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: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Dobro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Comparador de Placebo: Placebo
|
|
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Experimental: BI 1744 CL multiple rising doses
|
|
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Experimental: BI 1744 CL medium dose, females
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Prazo |
|---|---|
|
Number of patients with clinically significant changes in physical examination
Prazo: Baseline, day 32 (end-of-study examination)
|
Baseline, day 32 (end-of-study examination)
|
|
Number of patients with clinically significant changes in vital signs
Prazo: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Number of patients with clinically significant changes in 12-lead ECG (Electrocardiogram)
Prazo: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Number of patients with abnormal changes in laboratory tests
Prazo: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Changes in airway resistance (Raw) measured by body plethysmography
Prazo: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Changes in tremormetry parameters
Prazo: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Number of patients with adverse events
Prazo: Up to day 32
|
Up to day 32
|
|
Assessment of tolerability by the investigator on a 4-point scale
Prazo: Day 32 (end-of-study examination)
|
Day 32 (end-of-study examination)
|
Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
|
Cmax (maximum concentration of the analyte in plasma)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
tmax (time from dosing to maximum concentration)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
AUC (area under the concentration-time curve of the analyte in plasma at different time points)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
Aet1-t2(amount of analyte that is eliminated in urine from the time point t1 to time point t2)
Prazo: Up to 384 hours after drug administration
|
Up to 384 hours after drug administration
|
|
fet1-t2 (fraction of analyte eliminated in urine from time point t1 to time point t2)
Prazo: Up to 384 hours after drug administration
|
Up to 384 hours after drug administration
|
|
%AUCtz-∞ (the percentage of the AUC 0-∞ that is obtained by extrapolation)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
λz (terminal rate constant of the analyte in plasma)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
t½ (terminal half-life of the analyte in plasma)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
MRTih (mean residence time of the analyte in the body after inhalation)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
CL/F (apparent clearance of the analyte in the plasma after extravascular administration)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
Vz/F (apparent volume of distribution of the analyte during the terminal phase λz following an extravascular dose)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
CLR,t1-t2 (renal clearance of the analyte in plasma from the time point t1 until the time point t2)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
RA,Cmax,14 based on Cmax (Accumulation ratio of the analyte in plasma after multiple dose administration over a uniform dosing interval τ)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
RA,AUC,14 based on AUC0-τ
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
Cmin,ss (minimum measured concentration of the analyte in plasma at steady state over a uniform dosing interval τ)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
Cpre,ss (predose concentration of the analyte in plasma at steady state immediately before administration of the next dose)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
Linearity Index (LI)
Prazo: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Publicações e links úteis
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Links úteis
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
1 de janeiro de 2006
Conclusão Primária (Real)
1 de setembro de 2006
Datas de inscrição no estudo
Enviado pela primeira vez
20 de junho de 2014
Enviado pela primeira vez que atendeu aos critérios de CQ
20 de junho de 2014
Primeira postagem (Estimativa)
24 de junho de 2014
Atualizações de registro de estudo
Última Atualização Postada (Estimativa)
24 de junho de 2014
Última atualização enviada que atendeu aos critérios de controle de qualidade
20 de junho de 2014
Última verificação
1 de junho de 2014
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- 1222.2
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