- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT02247375
Pharmacokinetics, Safety and Efficacy of BIIL 284 BS in Patients With Rheumatoid Arthritis (RA)
23 septembre 2014 mis à jour par: 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.
Aperçu de l'étude
Statut
Complété
Les conditions
Type d'étude
Interventionnel
Inscription (Réel)
26
Phase
- La phase 1
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
18 ans à 65 ans (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Non
Sexes éligibles pour l'étude
Tout
La description
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
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Double
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Comparateur placebo: Placebo
|
|
|
Expérimental: Faible dose de BIIL 284 BS
|
|
|
Expérimental: Haute dose de BIIL 284 BS
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Changes from baseline in Mac-1 expression
Délai: 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
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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
Délai: Up to 4 weeks
|
Up to 4 weeks
|
|
Global assessment of tolerability by the patient on a 4-point scale
Délai: 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
Délai: Up to 14 days after start of treatment
|
Up to 14 days after start of treatment
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Changes from baseline in tender joint count (TJC)
Délai: 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)
Délai: 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)
Délai: 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
Délai: 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
Délai: 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
Délai: 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)
Délai: 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)
Délai: 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
Délai: 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)
Délai: 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
Délai: Up to 14 days after start of treatment
|
Up to 14 days after start of treatment
|
|
|
Number of withdrawals due to adverse events
Délai: Up to 4 weeks
|
Up to 4 weeks
|
|
|
Number of patients with clinically significant findings in laboratory adverse events
Délai: Up to 4 weeks
|
Up to 4 weeks
|
|
|
Number of patients with clinically significant findings in vital signs (blood pressure, pulse rate)
Délai: Up to 4 weeks
|
Up to 4 weeks
|
Collaborateurs et enquêteurs
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Parrainer
Publications et liens utiles
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Liens utiles
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude
1 janvier 2000
Achèvement primaire (Réel)
1 mai 2000
Dates d'inscription aux études
Première soumission
19 septembre 2014
Première soumission répondant aux critères de contrôle qualité
23 septembre 2014
Première publication (Estimation)
25 septembre 2014
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
25 septembre 2014
Dernière mise à jour soumise répondant aux critères de contrôle qualité
23 septembre 2014
Dernière vérification
1 septembre 2014
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 543.14
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