Usefulness of Non TNF Usage in RA Patients

NCT ID: NCT03784261

Last Updated: 2021-09-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE2

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-12-17

Study Completion Date

2024-12-16

Brief Summary

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The aim of this study is to examine the efficacy and adverse events in the following 3 groups in rheumatoid arthritis patients:

1. Sarilumab treatment for 12 months
2. Tocilizmab treatment for 12 months
3. Abatacept treatment for 12 months

Detailed Description

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Conditions

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Rheumatoid Arthritis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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SAR, usually subucutaneous injection every 2 weeks

Group Type ACTIVE_COMPARATOR

Drug: "Salirumab"

Intervention Type DRUG

To examine the effects of salirumab in RA patients

Drug: "Tocilizmab"

Intervention Type DRUG

To examine the effects of tocilizmab in RA patients

Drug: "Abatacept"

Intervention Type DRUG

To examine the effects of abatacept in RA patients

TCZ, usually subucutaneous injection every 2 weeks

Group Type ACTIVE_COMPARATOR

Drug: "Salirumab"

Intervention Type DRUG

To examine the effects of salirumab in RA patients

Drug: "Tocilizmab"

Intervention Type DRUG

To examine the effects of tocilizmab in RA patients

Drug: "Abatacept"

Intervention Type DRUG

To examine the effects of abatacept in RA patients

ABT, usually subucutaneous injection every week

Group Type ACTIVE_COMPARATOR

Drug: "Salirumab"

Intervention Type DRUG

To examine the effects of salirumab in RA patients

Drug: "Tocilizmab"

Intervention Type DRUG

To examine the effects of tocilizmab in RA patients

Drug: "Abatacept"

Intervention Type DRUG

To examine the effects of abatacept in RA patients

Interventions

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Drug: "Salirumab"

To examine the effects of salirumab in RA patients

Intervention Type DRUG

Drug: "Tocilizmab"

To examine the effects of tocilizmab in RA patients

Intervention Type DRUG

Drug: "Abatacept"

To examine the effects of abatacept in RA patients

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

・RA patients

Exclusion Criteria

* Not RA patients
* RA patients who are allergic to the drugs, refused to do this research, or who are pregnant
Minimum Eligible Age

20 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shinshu University

OTHER

Sponsor Role lead

Responsible Party

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Yukio Nakamura

Principle Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Yukio Nakamura

Matsumoto, Nagano, Japan

Site Status RECRUITING

Countries

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Japan

Facility Contacts

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Yukio Nakamura, MD, PhD

Role: primary

+81-263-37-2659

Other Identifiers

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NonTNF 2018

Identifier Type: -

Identifier Source: org_study_id

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