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

23 september 2014 uppdaterad av: 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.

Studieöversikt

Studietyp

Interventionell

Inskrivning (Faktisk)

26

Fas

  • Fas 1

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 65 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Dubbel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Placebo-jämförare: Placebo
Experimentell: Låg dos av BIIL 284 BS
Experimentell: Hög dos av BIIL 284 BS

Vad mäter studien?

Primära resultatmått

Resultatmått
Tidsram
Changes from baseline in Mac-1 expression
Tidsram: 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
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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
Tidsram: Up to 4 weeks
Up to 4 weeks
Global assessment of tolerability by the patient on a 4-point scale
Tidsram: 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
Tidsram: Up to 14 days after start of treatment
Up to 14 days after start of treatment

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Changes from baseline in tender joint count (TJC)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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)
Tidsram: 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)
Tidsram: 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
Tidsram: 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)
Tidsram: 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
Tidsram: Up to 14 days after start of treatment
Up to 14 days after start of treatment
Number of withdrawals due to adverse events
Tidsram: Up to 4 weeks
Up to 4 weeks
Number of patients with clinically significant findings in laboratory adverse events
Tidsram: Up to 4 weeks
Up to 4 weeks
Number of patients with clinically significant findings in vital signs (blood pressure, pulse rate)
Tidsram: Up to 4 weeks
Up to 4 weeks

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Användbara länkar

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 januari 2000

Primärt slutförande (Faktisk)

1 maj 2000

Studieregistreringsdatum

Först inskickad

19 september 2014

Först inskickad som uppfyllde QC-kriterierna

23 september 2014

Första postat (Uppskatta)

25 september 2014

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

25 september 2014

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

23 september 2014

Senast verifierad

1 september 2014

Mer information

Termer relaterade till denna studie

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