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Clinical Trials/NCT03161457
NCT03161457
Terminated
Phase 1

A Randomised, Double-blind, Parallel Group, Multicentre Study to Compare the Pharmacokinetics, Pharmacodynamics, Immunogenicity, Safety, and Efficacy of JHL1101 Versus EU-sourced MabThera® in Anti TNF Inadequate Responder Patients With Moderate to Severe Rheumatoid Arthritis (RA) on Background Methotrexate (MTX) Therapy

JHL Biotech, Inc.1 site in 1 country153 target enrollmentFebruary 27, 2017

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Rheumatoid Arthritis
Sponsor
JHL Biotech, Inc.
Enrollment
153
Locations
1
Primary Endpoint
Area under plasma concentration versus time curve (AUC)
Status
Terminated
Last Updated
6 years ago

Overview

Brief Summary

This is a multicentre, randomised, double-blind, parallel group study to compare the pharmacokinetics (PK), pharmacodynamics (PD), immunogenicity, safety, tolerability and efficacy of JHL1101 versus MabThera in subjects with moderate to severe RA who have previously failed at least 1 tumour necrosis factor alpha (TNF) inhibitor (i.e., intolerance or documented active disease despite at least 12 weeks treatment according to the TNF inhibitor-approved treatment and dosage), and are on concomitant treatment with MTX.

Detailed Description

This study will take place across approximately 31 centres across 12 countries and will randomise approximately 150 subjects as outpatients. The primary objective is to investigate and compare the pharmacokinetic profiles of JHL1101 and MabThera (rituximab). The secondary objectives are to investigate the safety, tolerability, and immunogenicity of JHL1101 versus MabThera, to investigate the pharmacodynamics profile of JHL1101 versus MabThera, and investigate the efficacy of JHL1101 versus MabThera.

Registry
clinicaltrials.gov
Start Date
February 27, 2017
End Date
April 16, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
JHL Biotech, Inc.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Moderate to severe active RA
  • Documented intolerance to or inadequate response to at least 12 weeks of treatment with the licensed regimen of at least one TNF inhibitor therapy
  • Women of childbearing potential must use a medically acceptable means of birth control and agree to continue its use during the study and for at least twelve months after the last dose of study drug.

Exclusion Criteria

  • History of a severe allergic reaction or anaphylactic reaction to a biological agent or history of hypersensitivity to any component of the study drug including known hypersensitivity or allergy to a murine product
  • Class IV as per the Classification of Global Functional Status in Rheumatoid Arthritis or wheelchair/bed-bound
  • Have any significant systemic involvement with RA such as vasculitis, pulmonary fibrosis or Felty's syndrome
  • History of or current inflammatory joint disease other than RA or other systemic disorder where the treatment or current or potential symptoms could confound the assessment of RA, with the exception of secondary Sjögren's syndrome
  • Concomitant or recent DMARD treatments for RA
  • Oral corticosteroids \>10mg/day prednisone equivalent or dose which has not been stable for the 4 weeks prior to Baseline
  • Receipt of an intra-articular or other injectable corticosteroid within 4 weeks prior to Screening
  • Intolerance or contraindications to IV corticosteroids
  • Use of NSAIDs which have not been at a stable dose within 2 weeks prior to Baseline.
  • Have undergone surgical treatments for RA including synovectomy and arthroplasty in more than 3 joints and/or within the last 8 weeks prior to Screening

Outcomes

Primary Outcomes

Area under plasma concentration versus time curve (AUC)

Time Frame: Day 0 through Week 52

Trough Concentration

Time Frame: Day 15

Maximum Concentration (Cmax)

Time Frame: Day 15

Secondary Outcomes

  • AUC(Up to Week 12)
  • Time to maximum plasma concentration(Day 0 through Week 52)
  • Cmax(Day 0 through Week 52)
  • Total body clearance(Day 0 through Week 52)
  • Volume of distribution(Day 0 through Week 52)
  • Terminal half life(Day 0 through Week 52)
  • Area under plasma concentration versus time curve(Week 2 to Week 24)
  • Incidence of treatment-related adverse events (safety)(Until End-of-Study follow-up at Week 52)
  • Immunogenicity(Baseline, Weeks 12, 16, 24, and 52)
  • Area under the depletion-time curve of CD19+ B-cell(Day 0 to Day 15, Day 0 to Week 12, Day 0 to Week 24, and Day 0 to Week 52 (end of study))
  • Change from Baseline in CD4+ T-cell counts(Day 0 through Week 52)
  • American College of Rheumatology (ACR) criteria 20, 50, 70 response rate(Weeks 4, 8, 12, 16, 24 and 52 and over time from Baseline to Week 52)
  • Swollen and tender joint count(From Baseline to Week 52)
  • Subject's assessment of arthritis pain(From Baseline to Week 52)

Study Sites (1)

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