- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT02247375
Pharmacokinetics, Safety and Efficacy of BIIL 284 BS in Patients With Rheumatoid Arthritis (RA)
23 settembre 2014 aggiornato da: 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.
Panoramica dello studio
Stato
Completato
Condizioni
Intervento / Trattamento
Tipo di studio
Interventistico
Iscrizione (Effettivo)
26
Fase
- Fase 1
Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
Da 18 anni a 65 anni (Adulto, Adulto più anziano)
Accetta volontari sani
No
Sessi ammissibili allo studio
Tutto
Descrizione
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
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Doppio
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Comparatore placebo: Placebo
|
|
|
Sperimentale: Basso dosaggio di BIIL 284 BS
|
|
|
Sperimentale: Alta dose di BIIL 284 BS
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Changes from baseline in Mac-1 expression
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: Up to 4 weeks
|
Up to 4 weeks
|
|
Global assessment of tolerability by the patient on a 4-point scale
Lasso di tempo: 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
Lasso di tempo: Up to 14 days after start of treatment
|
Up to 14 days after start of treatment
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Changes from baseline in tender joint count (TJC)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: Up to 14 days after start of treatment
|
Up to 14 days after start of treatment
|
|
|
Number of withdrawals due to adverse events
Lasso di tempo: Up to 4 weeks
|
Up to 4 weeks
|
|
|
Number of patients with clinically significant findings in laboratory adverse events
Lasso di tempo: Up to 4 weeks
|
Up to 4 weeks
|
|
|
Number of patients with clinically significant findings in vital signs (blood pressure, pulse rate)
Lasso di tempo: Up to 4 weeks
|
Up to 4 weeks
|
Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Pubblicazioni e link utili
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Collegamenti utili
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio
1 gennaio 2000
Completamento primario (Effettivo)
1 maggio 2000
Date di iscrizione allo studio
Primo inviato
19 settembre 2014
Primo inviato che soddisfa i criteri di controllo qualità
23 settembre 2014
Primo Inserito (Stima)
25 settembre 2014
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
25 settembre 2014
Ultimo aggiornamento inviato che soddisfa i criteri QC
23 settembre 2014
Ultimo verificato
1 settembre 2014
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 543.14
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .