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A Study to Evaluate the Safety and Efficacy of SM03 in Patients With Rheumatoid Arthritis Receiving Methotrexate

Phase 2
Completed
Conditions
Rheumatoid Arthritis
Interventions
Registration Number
NCT04192617
Lead Sponsor
SinoMab BioScience Ltd
Brief Summary

This study evaluated the safety and efficacy of SM03 compared to placebo in patients with active rheumatoid arthritis(RA) receiving methotrexate

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
156
Inclusion Criteria
  • Adult patients 18-75 years of age.
  • Rheumatoid arthritis (RA) for ≥ 12 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) ≥ 8 (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
  • Inadequate response to methotrexate, having received and tolerated at a dose of 7.5-20 mg/week for ≥ 12 weeks, at a stable dose over the past 4 weeks.
Exclusion Criteria
  • Rheumatic autoimmune disease other than RA.
  • Use of any biological DMARDs for RA within past 6 months.
  • Concurrent treatment with any Disease Modifying Anti-Rheumatic Drug (DMARD) other than methotrexate
  • Active infection, or history of serious or chronic infection

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
placebo*3Methotrexateplacebo: 600 mg intravenous (IV) on week 0,2, 4, and week 12,14,16; Methotrexate: 7.5-20 mg/wk oral.
SM03 600 mg*2MethotrexateSM03: 600 mg intravenous (IV) on week 0,2, and week 12,14; placebo: 600 mg intravenous (IV) on week 4 and16; Methotrexate: 7.5-20 mg/wk oral.
SM03 600 mg*2PlaceboSM03: 600 mg intravenous (IV) on week 0,2, and week 12,14; placebo: 600 mg intravenous (IV) on week 4 and16; Methotrexate: 7.5-20 mg/wk oral.
SM03 600 mg*3SM03SM03: 600 mg intravenous (IV) on week 0,2, 4, and week 12,14,16; Methotrexate: 7.5-20 mg/wk oral.
SM03 600 mg*3MethotrexateSM03: 600 mg intravenous (IV) on week 0,2, 4, and week 12,14,16; Methotrexate: 7.5-20 mg/wk oral.
placebo*3Placeboplacebo: 600 mg intravenous (IV) on week 0,2, 4, and week 12,14,16; Methotrexate: 7.5-20 mg/wk oral.
SM03 600 mg*2SM03SM03: 600 mg intravenous (IV) on week 0,2, and week 12,14; placebo: 600 mg intravenous (IV) on week 4 and16; Methotrexate: 7.5-20 mg/wk oral.
Primary Outcome Measures
NameTimeMethod
Percentage of Participants With American College of Rheumatology (ACR) 20 Response at Week 24Week 24

To achieve an ACR20 required at least a 20% improvement compared with Baseline in both tender joint counts (68 joints assessed for tenderness) and swollen joint counts (66 joints assessed for swelling), as well as a 20% improvement in three of the following five additional measurements:

* Physician's global assessment of disease activity (assessed using a 10 cm Visual Analog Scale \[VAS\]);

* Patient's global assessment of disease activity (assessed using a 10 cm VAS);

* Patient's assessment of pain (assessed using a 10 cm VAS);

* Health Assessment Questionnaire (HAQ; a patient completed questionnaire consisting of 20 questions, scored from 0-3);

* Acute phase reactant: C-reactive protein (CRP)

Secondary Outcome Measures
NameTimeMethod
Percentage of Participants With Adverse EventsWeek 0 to 24

Percentage of participants who reported an AE or SAE, a drug-related AE, who had an acute infusion reaction, an AE leading to study drug discontinuation, with an infection or serious infection, or who died.

Percentage of Participants With an ACR70 Response at Week 24Week 24

To achieve an ACR70 required at least a 70% improvement compared with Baseline in both tender joint counts (68 joints assessed for tenderness) and swollen joint counts (66 joints assessed for swelling), as well as a 70% improvement in three of the following five additional measurements:

* Physician's global assessment of disease activity (assessed using a 10 cm Visual Analog Scale \[VAS\]);

* Patient's global assessment of disease activity (assessed using a 10 cm VAS);

* Patient's assessment of pain (assessed using a 10 cm VAS);

* Health Assessment Questionnaire (HAQ; a patient completed questionnaire consisting of 20 questions, scored from 0-3);

* Acute phase reactant: C-reactive protein (CRP)

Change From Baseline in Disease Activity Score (DAS28-ESR) at Week 24Baseline and Week 24

The DAS28 is a composite score to measure disease activity in patients with rheumatoid arthritis, derived from the following variables:

* The number of swollen and tender joints assessed using the 28-joint count;

* Erythrocyte sedimentation rate (ESR);

* Patient's global assessment of disease activity measured on a 10 cm visual analog scale.

The DAS28 score ranges from zero to ten. A DAS28 score above 5.1 means high disease activity whereas a DAS28 less than or equal to 3.2 indicates low disease activity. Remission is achieved by a DAS28 lower than 2.6.

Percentage of Participants With European League Against Rheumatism (EULAR) Response at Week 24Week 24

A EULAR response reflects an improvement in disease activity and an attainment of a lower degree of disease activity based on the DAS28 score. The DAS28 score ranges from 0-10, with higher scores indicating more disease activity.

A Good Response is defined as an improvement (decrease) in the DAS28 of more than 1.2 compared with Baseline and attainment of a DAS28 score of less than or equal to 3.2.

A Moderate Response is defined as either:

an improvement (decrease) in the DAS28 of greater than 0.6 and less than or equal to 1.2 from Baseline and attainment of a DAS28 score of less than or equal to 5.1 or, an improvement (decrease) in the DAS28 of more than 1.2 from Baseline and attainment of a DAS28 score of greater than 3.2.

No Response is defined as either an improvement (decrease) in the DAS28 of less than or equal to 0.6, or an improvement (decrease) in the DAS28 of greater than 0.6 and less than or equal to 1.2 and attainment of a DAS28 of more than 5.1.

Percentage of Participants With an ACR50 Response at Week 24Week 24

To achieve an ACR50 required at least a 50% improvement compared with Baseline in both tender joint counts (68 joints assessed for tenderness) and swollen joint counts (66 joints assessed for swelling), as well as a 50% improvement in three of the following five additional measurements:

* Physician's global assessment of disease activity (assessed using a 10 cm Visual Analog Scale \[VAS\]);

* Patient's global assessment of disease activity (assessed using a 10 cm VAS);

* Patient's assessment of pain (assessed using a 10 cm VAS);

* Health Assessment Questionnaire (HAQ; a patient completed questionnaire consisting of 20 questions, scored from 0-3);

* Acute phase reactant: C-reactive protein (CRP)

Percentage of Participants With American College of Rheumatology (ACR) 20 Response at Week 4,8,12, 16Week 4,8,12,16

To achieve an ACR20 required at least a 20% improvement compared with Baseline in both tender joint counts (68 joints assessed for tenderness) and swollen joint counts (66 joints assessed for swelling), as well as a 20% improvement in three of the following five additional measurements:

* Physician's global assessment of disease activity (assessed using a 10 cm Visual Analog Scale \[VAS\]);

* Patient's global assessment of disease activity (assessed using a 10 cm VAS);

* Patient's assessment of pain (assessed using a 10 cm VAS);

* Health Assessment Questionnaire (HAQ; a patient completed questionnaire consisting of 20 questions, scored from 0-3);

* Acute phase reactant: C-reactive protein (CRP)

Trial Locations

Locations (1)

Peking Union Medical College Hostipal

🇨🇳

Beijing, China

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