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Pharmacokinetics, Safety and Efficacy of BIIL 284 BS in Patients With Rheumatoid Arthritis (RA)

23 de setembro de 2014 atualizado por: Boehringer Ingelheim

A Double-blind, Randomized, Three Parallel Group Placebo-controlled Study to Investigate Pharmacokinetics, Effect on Expression of CD11b/CD18 (Mac-1), as Well as Safety and Efficacy of Two Oral Doses of BIIL 284 BS (Dosage: 25 mg Daily, 150 mg Daily) in Patients With Rheumatoid Arthritis Over Two Weeks

Safety, pharmacokinetics, pharmacodynamics [CD11b/CD18 (Mac-1) expression] and efficacy.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Real)

26

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

18 anos a 65 anos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • Male and female from 18 to 65 years of age
  • Patients suffering from active rheumatoid arthritis as defined by the ARA criteria revised 1987

    --- At least 4 of the following 7 criteria must have been present:

    • morning stiffness in and around the joints lasting at least 1 hour before maximal improvement for at least 6 weeks
    • arthritis (soft tissue thickening or fluid - not bony overgrowth alone) of at least 3 joint areas for at least 6 weeks
    • arthritis of hand joints (at least one area swollen in a wrist, metacarpophalangeal (MCP) or proximal interphalangeal (PIP) joint) for at least 6 weeks
    • symmetric arthritis (observed by a physician) with simultaneous involvement of the joints on both sides of the body for at least 6 weeks
    • rheumatoid nodules (observed by a physician) over bony prominences or extensor surfaces or in juxta-articular regions
    • serum rheumatoid factor positive
    • x-ray changes typical of rheumatoid arthritis (erosions or unequivocal bony decalcification localised in or most marked adjacent to the involved joints)
  • Patient belonging to the RA functional class I, II or III
  • Patient's written informed consent

Exclusion Criteria:

  • Pregnancy (to be excluded by pregnancy test) or breast feeding
  • Women of childbearing potential not using adequate contraception
  • Treatment with methotrexate in the previous month or intended use during the trial period
  • Treatment with slow acting antirheumatic drugs (SAARDs)/disease-modifying antirheumatic drugs (DMARDs) other than parenteral gold, D-penicillamine, sulfasalazine, chloroquine / hydroxychloroquine corticosteroid during the last 2 months prior to study entry
  • Treatment with more than one SAARD/DMARD and/or corticosteroid during the last 2 months prior to study entry
  • Change in treatment with SAARDs/DMARDs during the last 2 months prior to study entry or intended change during the trial duration
  • Change in treatment with corticosteroids during the last month prior to study entry or intended change during the trial duration
  • Systemic treatment with corticosteroids at a dose higher than 10 mg/day or 0.2 mg/kg/day (prednisone equivalent), respectively (whichever is lower) during the last month prior to study entry or their intended use during the trial treatment period
  • Change in treatment with non-steroidal anti-inflammatory drugs (NSAIDs) during the last month prior to study entry or intended change during the trial duration
  • Treatment with EnbrelTM (etanercept) or experimental therapies during the last 3 months prior to study entry
  • Synovectomy and/or surgical treatment for RA in the previous month or during the trial
  • Clinical evidence of known severe cardiovascular, hepatic, renal, respiratory, metabolic, haematological, immunological, gastro-intestinal, hormonal or mental disorders
  • Any other rheumatological or non-rheumatological disease that could interfere with the evaluation of efficacy and safety
  • Patients with active malignant disease
  • Patients with chronic or acute infections during the previous month
  • Patients with abnormal, clinically relevant laboratory values not related to RA
  • Participation in another clinical trial during this study or during the previous month
  • Previous participation in this trial (i.e. having been allocated a randomized treatment number)
  • Patient unable to comply with the protocol
  • Patient with known drug abuse
  • Patient with known alcohol abuse

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
Experimental: Dose baixa de BIIL 284 BS
Experimental: Alta dose de BIIL 284 BS

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
Changes from baseline in Mac-1 expression
Prazo: Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Plasma concentrations of BIIL 284 BS, BIIL 260 BS, BIIL 315 ZW and BIIL 304 ZW
Prazo: Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Maximum concentration of the analyte in plasma (Cmax)
Prazo: Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Trough concentration of the analyte in plasma shortly before drug administration in a steady state dosing interval (Cpre,ss)
Prazo: Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Time to reach the maximum concentration of the analyte in plasma (tmax)
Prazo: Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Area under the concentration-time curve of the analyte in plasma (AUC)
Prazo: Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Number of patients with adverse events
Prazo: Up to 4 weeks
Up to 4 weeks
Global assessment of tolerability by the patient on a 4-point scale
Prazo: Up to 14 days after start of treatment
Up to 14 days after start of treatment
Global assessment of tolerability by investigator on a 4-point scale
Prazo: Up to 14 days after start of treatment
Up to 14 days after start of treatment

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Changes from baseline in tender joint count (TJC)
Prazo: Pre-dose, up to day 14 after start of treatment
Bilateral assessment of twenty-eight joints by e.g., pressure, joint manipulation etc.
Pre-dose, up to day 14 after start of treatment
Changes from baseline in swollen joint count (SJC)
Prazo: Pre-dose, up to day 14 after start of treatment
Twenty-eight joints were bilaterally assessed whether they are swollen or not
Pre-dose, up to day 14 after start of treatment
Changes from baseline in patient's current pain level assessment by visual analogue scale (VAS)
Prazo: Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Changes from baseline in patient's global assessment of disease activity by VAS
Prazo: Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Global assessment of disease activity by investigator on a 5-point scale
Prazo: Up to 14 days after start of treatment
Up to 14 days after start of treatment
Changes from baseline for patient's assessment of physical function
Prazo: Pre-dose, up to day 14 after start of treatment
Functional disability was measured using the disability section of the Health Assessment Questionnaire (HAQ)
Pre-dose, up to day 14 after start of treatment
Changes from baseline in erythrocyte sedimentation rate (ESR)
Prazo: Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Changes from baseline in C-reactive protein (CRP)
Prazo: Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Changes from baseline in american college of rheumatology (ACR) 20 score
Prazo: Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Changes from baseline in disease activity score (DAS)
Prazo: Pre-dose, up to day 14 after start of treatment
Pre-dose, up to day 14 after start of treatment
Global efficacy assessment by the patient on a 4-point scale
Prazo: Up to 14 days after start of treatment
Up to 14 days after start of treatment
Number of withdrawals due to adverse events
Prazo: Up to 4 weeks
Up to 4 weeks
Number of patients with clinically significant findings in laboratory adverse events
Prazo: Up to 4 weeks
Up to 4 weeks
Number of patients with clinically significant findings in vital signs (blood pressure, pulse rate)
Prazo: Up to 4 weeks
Up to 4 weeks

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 2000

Conclusão Primária (Real)

1 de maio de 2000

Datas de inscrição no estudo

Enviado pela primeira vez

19 de setembro de 2014

Enviado pela primeira vez que atendeu aos critérios de CQ

23 de setembro de 2014

Primeira postagem (Estimativa)

25 de setembro de 2014

Atualizações de registro de estudo

Última Atualização Postada (Estimativa)

25 de setembro de 2014

Última atualização enviada que atendeu aos critérios de controle de qualidade

23 de setembro de 2014

Última verificação

1 de setembro de 2014

Mais Informações

Termos relacionados a este estudo

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