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

23. september 2014 opdateret af: 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.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

26

Fase

  • Fase 1

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 65 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

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

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: Placebo
Eksperimentel: Lav dosis af BIIL 284 BS
Eksperimentel: Høj dosis af BIIL 284 BS

Hvad måler undersøgelsen?

Primære resultatmål

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

Sekundære resultatmål

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

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Hjælpsomme links

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. januar 2000

Primær færdiggørelse (Faktiske)

1. maj 2000

Datoer for studieregistrering

Først indsendt

19. september 2014

Først indsendt, der opfyldte QC-kriterier

23. september 2014

Først opslået (Skøn)

25. september 2014

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

25. september 2014

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

23. september 2014

Sidst verificeret

1. september 2014

Mere information

Begreber relateret til denne undersøgelse

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