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Tocilizumab for the Treatment of Refractory Behcet's Uveitis

Primary Purpose

Behcet Syndrome, Uveitis

Status
Terminated
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Tocilizumab (TCZ)
Sponsored by
Wenjie Zheng
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Behcet Syndrome focused on measuring Tocilizumab, Refractory uveitis

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All participants fulfill the the proposed International Criteria for BD, either ISG criteria(1990) or ICBD criteria(2013).
  • All participants present with refractory BDU , acute onset uveitis, either posterior segment involvement or panuveitis, with difficulty tapering corticosteroids while being treated with at least one of the commonly used immunosuppressants, without severe extraocular manifestations.

Exclusion Criteria:

  • Patients with impaired hepatic and renal function, other severe ocular diseases, active tuberculosis, viral hepatitis, malignancy, pregnancy will be excluded.

Sites / Locations

  • Peking Union Medical College Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Tocilizumab for refractory BDU

Arm Description

This study is a self-control study and all the participants will be enrolled in the interventional arm.

Outcomes

Primary Outcome Measures

Efficacy of Tocilizumab on BD Uveitis
Remission or deterioration of uveitis,based on intraocular inflammation evaluation

Secondary Outcome Measures

Intraocular inflammation evaluation BOS24 index
Visual acuity, anterior chamber cells, vitreous opacities, retinal inflammation, macular thickness, etc.
Corticosteroid-tapering effects
Whether corticosteroid dosage could be tapered to minimum dose.
Reduction of uveitis recurrence
Differences of recurrence between before and after treatment
Severity of uveitis on recurrence
Differences of severity of recurrence between before and after treatment
Improvement of quality of life
Record quality of life on questionnaire: BDCAF
Improvement of quality of life
Record quality of life on questionnaire: SF-36
Side effects of treatment
Record any side effects during intervention

Full Information

First Posted
April 21, 2018
Last Updated
March 17, 2021
Sponsor
Wenjie Zheng
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1. Study Identification

Unique Protocol Identification Number
NCT03554161
Brief Title
Tocilizumab for the Treatment of Refractory Behcet's Uveitis
Official Title
Efficacy and Safety of Tocilizumab in the Treatment of Refractory Uveitis in Patients With Behcet's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Terminated
Why Stopped
The study was terminated based on its primary and secondary outcome measures in three consecutive patients.
Study Start Date
May 10, 2018 (Actual)
Primary Completion Date
February 1, 2021 (Actual)
Study Completion Date
February 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Wenjie Zheng

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this single-center prospective study is to evaluate the efficacy and safety of Tocilizumab (TCZ), humanized monoclonal antibody against IL-6receptor, in the treatment of refractory Uveitis of Behçet's disease (BDU), to verify its effects on decreasing the dose of cortical steroids, and to determine whether it can reduce BDU recurrence.
Detailed Description
Uveitis of Behçet's disease (BDU) is the most common form of ocular manifestations, which is also the leading cause of irreversible visual impairment. The aim of the study is to Improve treatment strategy of the disease as well as to reduce blindness. Tocilizumab (TCZ) is a humanized antibody against IL-6 receptor, clinical trials on non-infectious uveitis and retrospective study on BDU has obtained expected results. This single-center prospective study is to evaluate the efficacy and safety of TCZ in the treatment of refractory BDU, to verify its effects on decreasing the dose of corticosteroids, and to determine whether it can reduce BDU recurrence.The investigators aim to enroll nine refractory BDU patients with acute onset uveitis, with difficulty tapering corticosteroids while being treated with at least one of the commonly used immunosuppressants. All participants will receive TCZ , oral corticosteroids and immunosuppressants will remain unchanged, intraocular injection will be avoided. During monthly follow-up, the investigators will measure and record intraocular inflammation status,as well as extraocular manifestations and the acute-phase reactants. The participants will continue to receive TCZ for six months, the primary end point is the efficacy four weeks after first dose of TCZ, secondary end points other than intraocular inflammation will be achieved on each follow-up visit, as quality of life improvements, side effects, recurrence of uveitis, and corticosteroids-tapering effects. On statistical analysis, the self-control treatment efficiency and recurrence rate difference will be determined using T-test of paired samples at a significance level of 0.05(2-sided). To ensure the interest of the participants, the study has been reviewed by the PUMCH ethics committee, and drug clinical research liability insurance was prepared.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Behcet Syndrome, Uveitis
Keywords
Tocilizumab, Refractory uveitis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
Tocilizumab is approved for the treatment of several inflammatory disease, this study tends to evaluate the response to TCZ in refractory BDU, thus it is a self-control study.
Masking
None (Open Label)
Allocation
N/A
Enrollment
3 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tocilizumab for refractory BDU
Arm Type
Experimental
Arm Description
This study is a self-control study and all the participants will be enrolled in the interventional arm.
Intervention Type
Biological
Intervention Name(s)
Tocilizumab (TCZ)
Intervention Description
Patients with refractory BD associated uveitis will receive Tocilizumab therapy, the efficacy and corticosteroids-tapering effects will be evaluated.
Primary Outcome Measure Information:
Title
Efficacy of Tocilizumab on BD Uveitis
Description
Remission or deterioration of uveitis,based on intraocular inflammation evaluation
Time Frame
four weeks
Secondary Outcome Measure Information:
Title
Intraocular inflammation evaluation BOS24 index
Description
Visual acuity, anterior chamber cells, vitreous opacities, retinal inflammation, macular thickness, etc.
Time Frame
each follow-up visit / every four weeks, up to six months
Title
Corticosteroid-tapering effects
Description
Whether corticosteroid dosage could be tapered to minimum dose.
Time Frame
six months
Title
Reduction of uveitis recurrence
Description
Differences of recurrence between before and after treatment
Time Frame
each follow-up visit / every four weeks, up to six months
Title
Severity of uveitis on recurrence
Description
Differences of severity of recurrence between before and after treatment
Time Frame
each follow-up visit / every four weeks, up to six months
Title
Improvement of quality of life
Description
Record quality of life on questionnaire: BDCAF
Time Frame
each follow-up visit / every four weeks, up to six months
Title
Improvement of quality of life
Description
Record quality of life on questionnaire: SF-36
Time Frame
each follow-up visit / every four weeks, up to six months
Title
Side effects of treatment
Description
Record any side effects during intervention
Time Frame
each follow-up visit / every four weeks, up to six months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All participants fulfill the the proposed International Criteria for BD, either ISG criteria(1990) or ICBD criteria(2013). All participants present with refractory BDU , acute onset uveitis, either posterior segment involvement or panuveitis, with difficulty tapering corticosteroids while being treated with at least one of the commonly used immunosuppressants, without severe extraocular manifestations. Exclusion Criteria: Patients with impaired hepatic and renal function, other severe ocular diseases, active tuberculosis, viral hepatitis, malignancy, pregnancy will be excluded.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wenjie Zheng, M.D.
Organizational Affiliation
Department of Rheumatology, Peking Union Medical College Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peking Union Medical College Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100730
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
29471416
Citation
Atienza-Mateo B, Calvo-Rio V, Beltran E, Martinez-Costa L, Valls-Pascual E, Hernandez-Garfella M, Atanes A, Cordero-Coma M, Miquel Nolla J, Carrasco-Cubero C, Loricera J, Gonzalez-Vela MC, Vegas-Revenga N, Fernandez-Diaz C, Demetrio-Pablo R, Dominguez-Casas LC, Luis Martin-Varillas J, Palmou-Fontana N, Hernandez JL, Gonzalez-Gay MA, Blanco R. Anti-interleukin 6 receptor tocilizumab in refractory uveitis associated with Behcet's disease: multicentre retrospective study. Rheumatology (Oxford). 2018 May 1;57(5):856-864. doi: 10.1093/rheumatology/kex480.
Results Reference
result
PubMed Identifier
28528519
Citation
Lopalco G, Fabiani C, Sota J, Lucherini OM, Tosi GM, Frediani B, Iannone F, Galeazzi M, Franceschini R, Rigante D, Cantarini L. IL-6 blockade in the management of non-infectious uveitis. Clin Rheumatol. 2017 Jul;36(7):1459-1469. doi: 10.1007/s10067-017-3672-z. Epub 2017 May 20.
Results Reference
result
Links:
URL
http://link.springer.com/article/10.1007%2Fs10067-017-3672-z
Description
Springerlink
URL
https://academic.oup.com/rheumatology/advance-article-abstract/doi/10.1093/rheumatology/kex480/4877959?redirectedFrom=fulltext
Description
Oxford Academic Rheumatology

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Tocilizumab for the Treatment of Refractory Behcet's Uveitis

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