Ultrasound as Imaging Biomarker of Early Response to Tocilizumab and Methotrexate in Very Early Rheumatoid Arthritis

Rheumatoid Arthritis Clinical Trial

— TOVERA  

Official title:

Ultrasound Scores as Imaging Biomarkers of Early Response to Subcutaneous Tocilizumab in Association With Methotrexate in Very Early Rheumatoid Arthritis (TOVERA)

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02837146
• Other study ID #: P1200_14
• Secondary ID: 2015-001246-28
• Status: Recruiting
• Phase: Phase 3
• First received: July 7, 2016
• Last updated: July 28, 2016
• Start date: December 2015
• Est. completion date: December 2019

Study information

• Verified date: July 2016
• Source: Université Catholique de Louvain
• Contact: Maria S Stoenoiu, MD, PhD
• Phone: +32 2 7645391
• Email: maria.stoenoiu[@]uclouvain.be
• Is FDA regulated: No
• Health authority: Belgium: Federal Agency for Medicines and Health Products, FAMHP
• Study type: Interventional

Clinical Trial Summary

This study is aimed at assessing the kinetics of the ultrasound (US) response in DMARD-naive very early rheumatoid arthritis (RA) patients treated with tocilizumab (TCZ) and methotrexate (MTX).

Description:

For most rheumatic autoimmune diseases, treatment has two components: induction of remission and maintenance (to prevent relapse). After screening (week -3 to 0), patients enter into a 3 week run-in period during which no glucocorticoid (GC) treatment is allowed. At week 0, if persistent synovitis is confirmed patients will enter the induction phase. During the induction phase all patients will receive TCZ and MTX from week 0 to week 24. After week 24, all patients will receive MTX.

Ultrasound (US) is increasingly used in rheumatic diseases, in particular in rheumatoid arthritis (RA). The great resolution of superficial musculoskeletal structures obtained by using high frequency transducers and the high sensitivity of colour Doppler (CD) and power Doppler (PD) techniques allow to detect synovial vascularisation, synovial hypertrophy (SH) and joint effusion (JE).

This is a pilot US trial that allow us to explore the hypothesis that an early US response may be predictive of later clinical response.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 45
• Est. completion date: December 2019
• Est. primary completion date: December 2018
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Diagnosis of RA fulfilling the 2010 EULAR/ACR (European League Against Rheumatism/ American College of Rheumatology classification criteria)

• Disease duration no longer than 12 months from the time of first swollen joint and no longer than 12 months from the time of initial diagnosis

• Age : 18-75 years

• Disease activity defined by a disease activity score DAS28-CRP > 3.2 or all must be met: tender joint count (TJC) of =4 and swollen joint count (SJC) =4

• US SH or PD synovitis scores >1 for at least 2 joints (MCP:2-5 or PIP:2-5 or CMC:2-5 or wrist joints or MTP:2-5 or ankle joints) and US SH or PD synovitis scores =1 for at least 1 other joint (MCP:2-5 or PIP:2-5 or or CMC:2-5 or wrist joints)

• Naïve to DMARDs (methotrexate, leflunomide, sulphasalazine) and naïve to any biologics or biosimilars.

Exclusion Criteria:

• History of other concomitant autoimmune disease such as lupus or psoriatic arthritis

• Meeting diagnostic criteria for any other rheumatic disease than RA (e.g. gout, Lyme disease, seronegative spondyloarthropathy including reactive arthritis, psoriatic arthritis, arthropathy or inflammatory bowel disease)

• Any previous treatment with :

1. Biologics: Etanercept, infliximab, certolizumab, golimumab, abatacept, adalimumab, anakinra, tocilizumab, tofacitinib, etc.

2. Any cell-depleting therapies, including investigational agents or approved therapies, some examples are CAMPATH, anti-CD4, anti-CD5, anti- CD3, anti-CD19 and anti-CD20

3. Intravenous gamma globulin, plasmapheresis or Prosorba column within 6 months of baseline.

4. Alkylating agents such as chlorambucil, or with total lymphoid irradiation

• Previous MCP arthroplasty or wrist arthrodesis. Participants who have undergone or are scheduled to undergo joint arthroplasties other than the MCP joints can be recruited in the study provided all other eligibility criteria are met.

• Current liver disease requiring medication

• Current symptoms of severe progressive or uncontrolled renal, hematologic, gastro-intestinal, pulmonary, cardiac, neurologic or cerebral disease whether or not related to rheumatoid arthritis, that would jeopardize inclusion in the protocol as judged by the clinician

• History of malignancy or lymphoproliferative disease, within the last 5 years, with the exception of basal cell or squamous cell carcinoma of the skin or carcinoma in situ of cervix which that has been fully excised/cured with no evidence of recurrence

• Concomitant diagnosis or history of diverticulitis, peptic ulcer disease, diverticulosis requiring antibiotic treatment or chronic ulcerative lower GI disease such as Crohn's disease, ulcerative colitis or other symptomatic lower GI conditions that might predispose to perforations

• Evidence of active or latent bacterial, viral, fungal (except for fungal infections of nail beds), mycobacterial or other opportunistic infections at the time of potential enrolment

• Any major episode of infection requiring hospitalisation or treatment with IV antibiotics within 4 weeks or oral antibiotics within 2 weeks of screening'

• Herpes zoster or cytomegalovirus infection that resolved less than 2 months before the informed consent was signed

• Subjects at risk of tuberculosis (TB) are excluded if any of the following is present:

• A history of active TB within the last 3 years, even if treated Latent TB that was not successfully treated = 4 weeks Current clinical radiographic, or laboratory evidence of active TB

• Subjects who received live vaccines within 4 weeks of the anticipated first dose of study medication. Live and live attenuated vaccines should not be given concurrently

• Subjects must agree not to take live attenuated vaccines (including seasonal nasal flu vaccine, varicella vaccine for shingles or chickenpox, MMR or MMRV, oral polio vaccine and vaccines for yellow fever, measles, mumps or rubella) thirty (30) days before the Screening Visit, throughout the duration of the trial and for sixty (60) days following the subject's last dose of study drug

• Subjects with positive test results for hepatitis B surface antigen or hepatitis C, or HIV detected with polymerase chain reaction or immunoblot assay

• Subjects with primary or secondary immunodeficiency

• History of severe allergic or anaphylactic reactions to human, humanized or murine monoclonal antibodies

• Major surgery within 8 weeks

• Patients with lack of peripheral venous access

• Pregnancy or breast-feeding

• Females of childbearing potential can only participate if using reliable contraception

• Intra-articular steroid injection in the joints assessed by US less than four weeks before screening

• Anticipated non-compliance with the protocol

Laboratory exclusion criteria

• Platelet count <100 x 109/l (100,000/mm3)

• Haemoglobin <85 g/l (8.5 g/dl; 5.3 mmol/l) (<8.0)

• White Blood Cells <3.0 x 109/l (3000/mm3) or >14,000/µl

• Absolute Neutrophil Count <2.0 x 109/l (2000/mm3)

• Absolute Lymphocyte Count <0.5 x 109/l (500/mm3)

• Positive Hepatitis BsAg, or Hepatitis C antibody

• Serum creatinine >1.4 mg/dl (124 µmol/l) in female patients and >1.6 mg/dl (141 µmol/l) in male patients. Patients with serum creatinine values exceeding limits may be eligible if their GFR is >30

• Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >1.5 times upper limit of normal (ULN)

• Total Bilirubin > ULN

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Arthritis
• Arthritis, Rheumatoid
• Rheumatoid Arthritis

Intervention

Biological:
• Tocilizumab (TCZ)
Induction phase: TCZ subcutaneously (162 mg weekly) from baseline to week 24

Drug:
• Methotrexate (MTX)
Induction and maintenance phase: Methotrexate 15-20 mg/week from baseline to week 54

Locations

Country	Name	City	State
Belgium	Maria S Stoenoiu	Brussels

Sponsors (1)

Lead Sponsor	Collaborator
Maria Stoenoiu

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in global ultrasound scoring system (GLOSS) at MCP (2-5 joints of both hands) and wrist joints	MCP=metacarpophalangeal; GLOSS scoring according to OMERACT: Grade 0 or normal=normal joint (no synovial hypertrophy (SH), no Doppler signal); Grade1 or minimal=minimal synovitis (minimal SH, with = grade 1 Doppler signal); Grade 2 or moderate=moderate synovitis (moderate SH, with = grade 2 Doppler signal or minimal SH and grade 2 Doppler signal); Grade 3 or severe=severe synovitis (severe SH with = grade 3 Doppler signal or minimal or moderate SH and grade 3 Doppler signal). Joints are scored 0 to 3, and the sum of individual joints scores represents the total GLOSS for a subject.	Baseline to weeks 2, 4, 8, 12, 16, 24, 32, 40, 54	No
Primary	The earliest time point at which improvement in GLOSS at MCP (2-5 joints of both hands) and wrists can be detected		Baseline to weeks 2, 4, 8, 12, 16, 24, 32, 40, 54	No
Secondary	GLOSS measured at 8 and 12 weeks is predictive to later clinical response at 24 and at 48 weeks		weeks 12, 24, 48	No
Secondary	Minimum set of joints to be monitored by US in order to adequately assess disease activity		Baseline to weeks 2, 4, 8, 12, 16, 24, 32, 40, 54	No
Secondary	Change in GLOSS for the whole US joint set		Baseline to weeks 2, 4, 8, 12, 16, 24, 32, 40, 54	No
Secondary	Change in power Doppler (PD) scores for the whole US joint set		Baseline to weeks 2, 4, 8, 12, 16, 24, 32, 40, 54	No
Secondary	Change in gray-scale (GS) scores for the whole US joint set		Baseline to weeks 2, 4, 8, 12, 16, 24, 32, 40, 54	No
Secondary	Change in joint effusion (JE) scores for the whole US joint set		Baseline to weeks 2, 4, 8, 12, 16, 24, 32, 40, 54	No
Secondary	Total PD score measured at 8 and 12 weeks is predictive to later clinical response at 24 and at 48 weeks		weeks 8, 12 , 24, 48	No
Secondary	No radiographic progression assessed by Sharp/vdHeijde score		baseline to week 54	No
Secondary	No new radiographic joint erosion at hands, wrists, ankles, feet		baseline to week 54	No
Secondary	No new radiographic joint chondrolysis at hands, wrists, ankles, feet		baseline to week 54	No
Secondary	No new swollen joint assessed by clinical examination		baseline to week 54	No
Secondary	No new swollen joint assessed by ultrasound examination		baseline to week 54	No
Secondary	DAS28 during the induction and maintenance phase		baseline to week 2, 4, 8, 12, 16, 24, 48, 54	No
Secondary	SDAI during the induction and maintenance phase		baseline to week 2, 4, 8, 12, 16, 24, 48, 54	No
Secondary	CDAI during the induction and maintenance phase		baseline to week 2, 4, 8, 12, 16, 24, 48, 54	No
Secondary	Swollen joint count score during the induction and maintenance phase		baseline to week 2, 4, 8, 12, 16, 24, 48, 54	No
Secondary	Tender joint count score for disease activity during the induction and maintenance phase		baseline to week 2, 4, 8, 12, 16, 24, 48, 54	No
Secondary	Patient visual analog score for disease activity during the induction and maintenance phase		baseline to week 2, 4, 8, 12, 16, 24, 48, 54	No
Secondary	Physician visual analog score for disease activity during the induction and maintenance phase		baseline to week 2, 4, 8, 12, 16, 24, 48, 54	No
Secondary	Number of patients fulfilling ACR/EULAR (2011) remission criteria during the induction and maintenance phase		baseline to week 2, 4, 8, 12, 16, 24, 48, 54	No
Secondary	Health assessment questionnaire(HAQ) score during the induction and maintenance phase		baseline to week 2, 4, 8, 12, 16, 24, 48, 54	No
Secondary	Number of participants with serious adverse events(SAEs), with treatment-related SAEs, with discontinuations due to SAEs, with adverse events (AEs) with treatment-related AEs, with discontinuations due to AEs, death as outcome.		Days 1 to 365 days	Yes