A randomised, double-blind, placebo-controlled trial for establishing safety, tolerability, pharmacokinetics, pharmacodynamics and clinical efficacy of multiple subcutaneous doses of BI 655064 in healthy volunteers and in rheumatoid arthritis patients with prior inadequate response to methotrexate therapy

Part 1 (HVs):;1. Healthy males and females according to the investigator*s assessment, as based on the following criteria: a complete medical history including a physical examination, vital signs (BP, PR), 12-lead ECG, and clinical laboratory tests;2. Age * 18 and * 60 years;3. Body Mass Index * 18.5 and * 29.9 kg/m2;4. Signed and dated written informed consent prior to admission to the study in accordance with GCP and the local legislation;5. Female subjects who meet any of the following criteria from at least 30 days before the first study drug administration and until 30 days after trial completion: - using adequate contraception, e.g. any of the following methods plus condom: implants, injectables, combined oral contraceptives, intrauterine device (IUD) - sexually abstinent - have a vasectomised sexual partner (vasectomy at least 1 year prior to enrolment) - surgically sterilised (including hysterectomy) - postmenopausal defined as at least 1 year of spontaneous amenorrhea (in questionable cases a blood sample with simultaneous levels of follicle stimulating hormone (FSH) above 40 U/L and estradiol below 30 ng/L is confirmatory);Part 2 (RA Patients):;1. Age * 18 and * 70 years;2. Patients classified as having RA according to the 1987 ACR Classification Criteria;3. Insufficient clinical response to methotrexate defined as moderate/high active disease after oral or s.c MTX treatment given continuously for at least 3 months and for the last 6 weeks before screening at a stable weekly dose *15mg. For patients who do not tolerate the minimum weekly dose of at least 15 mg due to side effects, a stable weekly dose as low as 7.5 mg is also permitted;4. Moderate or highly active disease defined as DAS28 4v-CRP * 3.5 with * 6 tender and * 6 swollen joints out of 68/66 joint count at screening and confirmed by * 6 tender and * 6 swollen joints out of 68/66 joint count at randomisation visit (Visit 2);5. Serum CRP level * 0.8 mg/dL or ESR * 28 mm/1h at screening;6. Anti-CCP2 or Rheumatoid Factor positivity according to the limits of the assay used at screening;7. Female patients who meet any of the following criteria from at least 30 days before the first study drug administration and until at least 6 months after last dose of MTX taken in the current trial: - using adequate contraception, e.g. any of the following methods plus condom: implants, injectables, combined oral contraceptives, intrauterine device (IUD) - sexually abstinent - have a vasectomised sexual partner (vasectomy at least 1 year prior to enrolment) - surgically sterilised (including hysterectomy) - postmenopausal defined as at least 1 year of spontaneous amenorrhea (in questionable cases a blood sample with simultaneous levels of follicle stimulating hormone (FSH) above 40 U/L and estradiol below 30 ng/L is confirmatory) OR Male patients who: - are documented to be sterile or consistently and correctly use a condom while their female partners (if of childbearing potential) agree to use any of the following adequate contraception methods: implants, injectables, combined oral contraceptives, intrauterine device (IUD) from the date of screening until at least 6 months after the last dose of MTX taken in the current trial. - don*t donate any sperm sample for procreation purposes, from the date of screening until at least 6 months after last dose of MTX taken in the current trial. It is the responsibility of the male patient to ensure that his partner does not become pregnant during all the study duration. Female partners of childbearing potential must perform monthly urine pregnancy tests from the date of screening until at least 6 months after last dose of MTX taken in the current trial.;8. Signed and dated written informed consent prior to admission to the study in accordance with GCP and the local legislation

Part 1 (HVs):;1. Any finding in the medical examination (including BP, PR or ECG) deviating from normal and judged clinically relevant by the investigator;2. Any laboratory value outside the reference range that the investigator considers to be of clinical relevance;3. Any evidence of a concomitant disease judged clinically relevant by the investigator;4. Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders;5. Diseases of the central nervous system (such as epilepsy), other neurological disorders or psychiatric disorders;6. History of relevant orthostatic hypotension, fainting spells, or blackouts;7. History of relevant allergy/hypersensitivity (including allergy to the trial medication or its excipients);8. Intake of drugs with a long half-life (>24 hours) within 30 days or less than 10 half-lives of the respective drug prior to administration of trial medication;9. Within 10 days prior to administration of trial medication, use of drugs that might reasonably influence the results of the trial;10. Participation in another trial with investigational drug administration within 60 days prior to administration of trial medication;11. Smoker (more than 10 cigarettes or 3 cigars or 3 pipes/day);12. Alcohol abuse (consumption of more than 140 g/week in females and 210 g/week in males);13. Drug abuse or positive drug screen;14. Blood donation (more than 100 mL within 30 days prior to administration of trial medication or intended during the trial);15. Intention to commence new exercise regimen within one week prior to administration of trial medication or during the trial;16. Inability to comply with dietary regimen of trial site;17. Chronic or relevant acute infections, including but not limited to HIV, Hepatitis B and C and tuberculosis (including a history of clinical TB and/or a positive QuantiFERON TB-Gold test);18. Subject is assessed by the investigator as unsuitable for inclusion e.g. considered not able to understand and comply with study requirements or has a condition that would not allow safe participation in the study;19. Positive pregnancy test, pregnancy or plans to become pregnant within 30 days after study completion;20. Lactation;Part 2 (RA patients):;Part 1 exclusion criteria 7, 9, 12, 13 and 17-20 plus:;1. Current or previous use of more than two anti-TNF biologic drugs or use of other biologic agent targeting any other approved mechanism (any biologic drug with mechanism of action other than direct anti-TNF blockade (e.g. CTLA4, anti-IL6, or anti CD-20) or new oral compounds targeting any other approved mechanism (e.g. JAK inhibitors) for treating RA;2. Current or previous participation in a clinical trial testing an investigational drug for RA within 3 months prior to screening or within 5 half-lives of the investigational drug, whichever is longer except of previous participation in trials testing NSAIDs, corticosteroids, analgesics or patients documented as receiving placebo in previous RA trials;3. DAS28 <3.2 in at least 2 occasions during the last 6 months before screening
Note: DAS28 results during the last 6 months before screening visit will be provided as source documents if available. However, patients with less than 2 DAS28 results available during this time will not be excluded. ;4. RA patients with severe disability (functional class IV) or with confirmed severe systemic manifestations e.g. known amyloidosis, Felty*s syndrome, lymphoproliferative disorders, rheumatoid vasculitis;5. Treatment with any standard DMARD except MTX (including but not limited to sulfasalazine, leflunomide, hydroxychloroquine, D-penicillamine, azathioprine, cyclosporin, gold salts) continuing after randomisation
Note: If patient is on treatment with any other standard DMARD (except MTX) at the time of the screening visit, this should be tapered and stopped before randomisation. MTX should be continued during the screening period at a stable dose between 15-25mg per week. For patients who do not tolerate the minimum weekly dose of at least 15 mg due to side effects, a stable weekly dose as low as 7.5 mg is also permitted;6. Impaired hepatic function, defined as serum AST/ALT, bilirubin or alkaline phosphatase levels > 2 x ULN ;7. Impaired renal function defined as calculated creatinine clearance < 50ml/min;8. Pre-existing blood dyscrasias e.g. bone marrow hypoplasia, significant anaemia, leucopenia or thrombocytopenia;9. Hypersensitivity to MTX or any of its excipients;10. Previous intolerance to MTX as the main cause for stopping treatment (instead of lack of efficacy);11. Any active or suspected malignancy or history of documented malignancy within the last 5 years before screening, except appropriately treated basal cell carcinoma of the skin or in situ carcinoma of uterine cervix.