A Study of Two Doses of MRC375 in Moderate to Severe Rheumatoid Arthritis Patients
9 mai 2014 mis à jour par: Molecular Research Center, Inc.
A 24-week, Phase 2, Double-blind, Placebo-controlled, Randomized Study to Assess the Safety and Efficacy of 2 Doses of MRC375 in Patients With Moderate to Severe Rheumatoid Arthritis
This study will treat moderate to severe rheumatoid arthritis with MRC375 (either 75 mg 3 times a day, 150 mg 3 times a day or placebo 3 times a day)in patients 18 years of age or older that can be currently on low doses of methotrexate or can stop treatment of current RA medications to enter the study.
Safety of MRC375 will also be evaluated.
There are up to 8 clinic visits over 24 weeks.
Aperçu de l'étude
Statut
Inconnue
Les conditions
Intervention / Traitement
Description détaillée
This is a double-blind, randomized, placebo-controlled study to assess the safety and efficacy of MRC375 at 75 mg or 150 mg with matching placebo (taken tid with meal or light snack) in patients with moderate to severe RA. Patients will be randomized to one of the following study arms for 24 weeks:
- Treatment 1, Placebo: 2 tablets taken tid
- Treatment 2, MRC375: 1 tablet of 75 mg tetracycline HCL plus 1 matching placebo tablet taken tid. Total daily dose = 225 mg.
- Treatment 3, MRC375: 2 tablets of 75 mg tetracycline HCL taken tid. Total daily dose = 450 mg.
Study medication should be taken within 30 minutes of a meal or light snack (either before or after).
Type d'étude
Interventionnel
Inscription (Anticipé)
300
Phase
- Phase 2
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
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Alabama
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Mobile, Alabama, États-Unis, 36608
- Mobile Diagnostic Center Rheumatology
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California
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Long Beach, California, États-Unis, 90806
- Valerius Medical Group
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Los Alamitos, California, États-Unis, 90720
- Trial Concierge/Pacific Clinical Studies
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Los Angeles, California, États-Unis, 90036
- Axis Clinical Trials
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Florida
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Edgewater, Florida, États-Unis, 32132
- Riverside Clinical Research
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Miami, Florida, États-Unis, 33156
- Global Clinical Professionals
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Palm Harbor, Florida, États-Unis, 34684
- The Arthritis Center
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Summerfield, Florida, États-Unis, 34491
- Lakeview Medical Research
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Kansas
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Lenexa, Kansas, États-Unis, 66219
- Analan Clinical Research
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Kentucky
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Owensboro, Kentucky, États-Unis, 42303
- Trial Concierge
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Nebraska
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Omaha, Nebraska, États-Unis, 68114
- Quality Clinical Research, Inc.
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Nevada
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Las Vegas, Nevada, États-Unis, 89123
- Advanced Biomedical Research of America
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Reno, Nevada, États-Unis, 89502
- Arthritis Center of Reno
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North Carolina
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Salisbury, North Carolina, États-Unis, 28144
- PMG Research of Salisbury
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Ohio
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Dayton, Ohio, États-Unis, 45439
- Providence Health Partners
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Middleburg Heights, Ohio, États-Unis, 44130
- Paramount Medical Research & Consulting, LLC
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Virginia
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Williamsburg, Virginia, États-Unis, 23185
- The Center for Excellence in Aging and Geriatric Health
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Washington
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Kennewick, Washington, États-Unis, 99336
- Apex Clinical Research
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Olympia, Washington, États-Unis, 98502
- South Puget Sound Clinical Research Center
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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 et plus (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Non
Sexes éligibles pour l'étude
Tout
La description
Inclusion Criteria:
- Is 18 years of age
- Is diagnosed with moderate to severe adult onset RA > = 6 months duration, as defined by the 1987 ACR classification criteria
Has moderate to severe RA as defined by:
- ≥4 tender joints/painful (28 joint count) at screening
- ≥4 swollen joints (28 joint count) at screening
- Has a Health Assessment Questionnaire (HAQ) of >0
- Has a physician global assessment (Likert scale) of >0
- Has a patient global assessment of pain (Likert scale) of >0
- Has a patient assessment of pain (Likert scale) of >0
Has stable doses of the following allowable medications during the study, if applicable:
- Stable dose of NSAIDs or other analgesics for at least 2 weeks prior to administration of study drug at regulatory approved doses
- Stable dose of methotrexate 7.5 mg to 25 mg/day once weekly for at least 6 weeks prior to administration of study drug (no changes in dosing regimen for 4 weeks prior to screening)
- Stable dose of hydroxychloroquine either monotherapy or in combination with methotrexate 8 weeks prior to administration of study drug
- Is a non-pregnant, non-lactating female who is postmenopausal, naturally or surgically sterile, or who agree to use effective contraceptive methods throughout the course of the study. Postmenopausal is defined as at least 12 months natural spontaneous amenorrhea
If female of childbearing potential, must agree to use one of the following acceptable birth control methods:
- Surgically sterile (bilateral tubal ligation with surgery at least 6 weeks prior to screening, hysterectomy, or bilateral oophorectomy);
- Intrauterine device (IUD) in place for at least 3 months prior to first dose of study drug;
- Abstinence (not having sexual intercourse);
- Barrier method (condom or diaphragm) with spermicide for at least 14 days prior to screening and through study completion;
- Stable hormonal contraceptive for at least 3 months prior to study and through study completion
- If female of childbearing potential, has a negative serum hCG pregnancy test at screening
- Is able to swallow whole tablets of orally administered medication
- Is able to understand and provide signed informed consent.
Exclusion Criteria:
- Has been diagnosed with any other inflammatory arthritis (eg, psoriatic arthritis)
- Has a secondary type of arthritis (eg, osteoarthritis) that would interfere with study evaluations
Has taken the following drugs within the timeframe specified below:
- Infliximab, etanercept, adalimumab, abatacept, or other biological therapies (except rituximab) - Within 12 weeks prior to the administration of study drug;
- Rituximab - Within 12 months prior to the administration of study drug;
- Disease-modifying antirheumatic drugs (DMARDs) or other anti-rheumatic therapies not specified above including but not limited to: sulfasalazine, gold, leflunomide, penicillamine, dapsone, azathioprine, 6-mercaptopurine, chlorambucil, cyclophosphamide, cyclosporin, mycophenolate mofetil - Within 12 weeks prior to the administration of study drug;
- Any steroids (glucocorticoids); glucocorticoids must be discontinued for at least 4 weeks prior to administration of study drug. Intraarticular, intramuscular, or intravenous glucocorticoids must not have been given at least 6 weeks prior to administration of study drug.
- Note: Use of probiotics is allowed and is NOT an exclusion criterion.
- Has a uncontrolled symptoms of fibromyalgia with sufficient symptoms requiring treatment (NOTE: patients on a stable dose of treatment for symptoms of fibromyalgia ≥ 4 weeks will be allowed in the study.)
- Has a history of allergic reaction to tetracycline or other related drugs
- Had major surgery or trauma within 28 days prior to screening
- Is concurrently using minocycline or doxycycline (washout of 4 weeks required before the administration of study drug)
- Patients who are on chronic antibiotics or who are on antibiotics for GI infections (such as Clostridium difficile)
- Has clinically significant ECG abnormalities
- Has any clinically significant abnormal laboratory test results found during medical screening including: AST or ALT > 2 x upper limit of normal or serum creatinine > 2.0 mg/dL
- Has clinically significant history or presence of any gastrointestinal pathology (eg, chronic diarrhea, inflammatory bowel disease, acute diverticulitis), irritable bowel syndrome, unresolved gastrointestinal symptoms (eg. diarrhea, vomiting, symptoms of acute diverticulitis), liver or kidney disease, gastric bypass, gastric stapling, use of Lap-Band®, or other conditions known to or which might interfere with the absorption, distribution, metabolism, or excretion of the drug
- Has any historical or active neurological, endocrine, cardiovascular, pulmonary, hematological, psychiatric, or metabolic disease that is considered clinically significant by the Investigator
- Has known history of HIV, hepatitis B or C (patients that have positive hepatitis B serology due to prior vaccination will be allowed in the study)
- Has an active malignancy of any type or history of malignancy. Patients who have a history of a successfully treated non-metastatic cutaneous squamous cell or basal cell carcinoma (ie. non melanoma skin cancer)and/or localized carcinoma in situ of the cervix are eligible. Patients with a history of other malignancies that have been treated and who have no evidence of recurrence for at least 5 years before study enrollment are also eligible.
- Has difficulty swallowing tablets
- Is ACR Functional Class IV (limited ability to perform usual self-care, vocational, and avocational activities)
- Has known or suspected pregnancy, planned pregnancy, or lactation (for female patients)
- Has clinically significant mental illness (to be determined by the Investigator)
- Has a history in the last 2 years or current evidence of abuse of illicit drugs, prescription medications, or alcohol that, in the opinion of the Investigator, would interfere with adherence to study requirements. Has exposure to any investigational agent within 30 days prior to study entry.
- Was previously enrolled in this study
- Has recent history of bacterial intestinal tract infection (gastroenteritis, colitis, diverticulitis, appendicitis)
- Has a condition the Investigator believes would interfere with the ability to provide informed consent or comply with study instructions, or that might confound the interpretation of the study results or put the patient at undue risk
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: Quadruple
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Comparateur placebo: Placebo
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Matching Placebo 3 times a day for 24 weeks.
Early escape at week 16,20.
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Expérimental: MRC375 75 mg
MRC375 (enteric coated Tetracycline) 75 mg 3 times a day
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MRC 375 (enteric coated Tetracycline) 75mg 3 times a day for 24 weeks.
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Expérimental: MRC375 150mg
MRC375 (enteric coated Tetracycline) 150mg 3 times a day for 24 weeks.
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MRC375 (enteric coated Tetracycline) 150mg 3 times a day for 24 weeks
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Efficacy evaluated of both doses of MRC375 compared to placebo after 24 weeks of treatment as measured by the rate of achievement of 20% improvement in ACR criteria
Délai: 24 weeks
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evaluate efficacy of both doses of MRC375 compared to placebo after 24 weeks of treatment, as measured by a rate of achievement of 20% improvement in American College of Rheumatology (ACR) criteria (ACR20) at Week 24
|
24 weeks
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Safety and tolerability of both doses of MRC375
Délai: 24 weeks
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evaluate the safety and tolerability of both doses of MRC375 tablets
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24 weeks
|
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Compare the Efficacy of two doses of MRC375 when compared to a placebo for the change from baseline screening in each of the individual ACR components measuring RA after 24 weeks of treatment
Délai: 24 weeks
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compare the efficacy of 2 doses of MRC375 tablets (75 mg tid and 150 mg tid) when compared to placebo for the change from baseline screening in each of the individual ACR components measuring rheumatoid arthritis (RA) after 24 weeks of treatment.
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24 weeks
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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
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 novembre 2011
Achèvement primaire (Anticipé)
1 juillet 2014
Achèvement de l'étude (Anticipé)
1 juillet 2014
Dates d'inscription aux études
Première soumission
2 août 2011
Première soumission répondant aux critères de contrôle qualité
2 août 2011
Première publication (Estimation)
3 août 2011
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
12 mai 2014
Dernière mise à jour soumise répondant aux critères de contrôle qualité
9 mai 2014
Dernière vérification
1 mai 2014
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- MRC2011-001
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .