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Clinical Trials/NCT04704492
NCT04704492
Completed
Phase 1

An Open-label, Multiple-dose Study to Assess the Pharmacokinetics, Pharmacodynamics, Preliminary Clinical Activity and Safety of Human Mouse Chimeric Anti-CD22 Monoclonal Antibody (SM03) in Patients With Rheumatoid Arthritis

SinoMab BioScience Ltd1 site in 1 country8 target enrollmentAugust 14, 2012

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Rheumatoid Arthritis
Sponsor
SinoMab BioScience Ltd
Enrollment
8
Locations
1
Primary Endpoint
Systemic Clearance (CL)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This was an open phase I trial to evaluate the pharmacokinetic, pharmacodynamic, safety and clinical activity profiles of anti-CD22 monoclonal antibody SM03 in patients with active RA.

Detailed Description

This was an open phase I trial to evaluate the PK, PD, safety,tolerability, efficacy, and immunogenicity of SM03 in patients with RA. The total study duration was approximately 16 weeks for each participant, including a screening period of maximally 4 weeks, a multiple-dose period of 2 weeks (day 0 \~ day 14), and a post-treatment follow-up period of 10 weeks (day 15 \~ day 84).

Registry
clinicaltrials.gov
Start Date
August 14, 2012
End Date
December 16, 2013
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
SinoMab BioScience Ltd
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Rheumatoid arthritis (RA) for ≥ 6 months, diagnosed according to the revised 1987 American College of Rheumatology (ACR) criteria for the classification of rheumatoid arthritis.
  • Moderate to severe active RA with swollen joint count (SJC) ≥ 6 (66 joint count), and tender joint count (TJC) ≥ 8 (68 joint count) at screening and baseline.
  • At screening, either C-reactive protein (CRP) ≥ 0.6 mg/dL (6 mg/L), or Erythrocyte sedimentation rate (ESR) ≥ 28 mm/hour, or Morning stiffness of joint for ≥ 45 minutes.
  • Receiving methotrexate (MTX) 7.5 - 25mg/week (oral) for at least 12 weeks, at a stable dose over the past 4 weeks.

Exclusion Criteria

  • Females who are pregnant, breastfeeding, or planning a pregnancy during the Treatment Period of and 12 months after the last infusion of study drug.
  • Rheumatic autoimmune disease other than RA.
  • Use of any biological DMARDs for RA within past 6 months.
  • Active infection, or history of serious or chronic infection.
  • Any significant cardiac disease, moderate to severe chronic obstructive pulmonary disease.
  • Allergy or sensitivity to components of the drug vial or any of the materials used for infusion

Outcomes

Primary Outcomes

Systemic Clearance (CL)

Time Frame: Week 0 to 12

Pharmacokinetic endpoint: Systemic Clearance (CL)

Peak Plasma Concentration (Cmax)

Time Frame: Week 0, 2

Pharmacokinetic endpoint: Peak Plasma Concentration (Cmax)

Terminal Half-life (T1/2)

Time Frame: Week 0 to 12

Pharmacokinetic endpoint:Terminal Half-life (T1/2)

Time to Maximum Plasma Concentration (Tmax)

Time Frame: Week 0,2

Pharmacokinetic endpoint: Time to Maximum Plasma Concentration (Tmax)

Area Under the Concentration Time Cure(AUC0-t)

Time Frame: Week 0 to 12

Pharmacokinetic endpoint: Area Under the Concentration Time Cure(AUC0-t)

Secondary Outcomes

  • Number of Participants Who Experienced at Least One Adverse Event(Week 0 to 12)
  • Change From Baseline in Disease Activity Score (DAS28-ESR) at Week 12(Week 0,2,4,8,12)
  • Number of ACR20, ACR50, and ACR70 Responders at Week 12(Week 2,4,8,12)

Study Sites (1)

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