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Tacrolimus Treatment for Refractory Autoimmune Cytopenia

Primary Purpose

Autoimmune Hemolytic Anemia, Pure Red Cell Aplasia, Evans Syndrome

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Tacrolimus
Sponsored by
Peking Union Medical College Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Autoimmune Hemolytic Anemia focused on measuring Tacrolimus, Refractory autoimmune cytopenia, Prospective study

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Refractory autoimmune cytopenia, including autoimmune hemolytic anemia, pure red cell aplasia, Evans syndrome.
  • 18-80 years old.
  • No response or intolerant to first and second line therapies.
  • ECOG Performance Status of 0-2
  • Written informed consent.

Exclusion Criteria:

  • Other diseases which might cause hematological abnormalities.
  • Response and well tolerate to first or second line therapy.
  • Patients who are under 18-year-old or over 80-year-old.
  • Pregnant or lactating.
  • Patients unwilling to or unable to comply with the protocol.

Sites / Locations

  • Peking Union Medical College HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Efficiency of tacrolimus on autoimmune cytopenia

Arm Description

A prospective research of the tacrolimus efficiency on refractory autoimmune cytopenia patients. Dosage: 1mg bid and tacrolimus trough targets were 5-10 ng/ml throughout the study. Medication time should last at least 6 months.

Outcomes

Primary Outcome Measures

Hemoglobin level
Hemoglobin level in g/L
Platelet count
Platelet count in /L

Secondary Outcome Measures

Hemoglobin level
Hemoglobin level in g/L
Platelet count
Platelet count in /L

Full Information

First Posted
April 16, 2019
Last Updated
December 1, 2019
Sponsor
Peking Union Medical College Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03918265
Brief Title
Tacrolimus Treatment for Refractory Autoimmune Cytopenia
Official Title
Tacrolimus Treatment for Refractory Autoimmune Cytopenia
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Unknown status
Study Start Date
May 4, 2019 (Actual)
Primary Completion Date
August 10, 2020 (Anticipated)
Study Completion Date
November 10, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Peking Union Medical College Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Autoimmune cytopenia, including autoimmune hemolytic anemia (AIHA), pure red cell aplasia (PRCA), Evans syndrome (ES), usually has good responses to steroids therapies as first line, but there is a considerable percentage of patients who relapse, become refractory or dependent on steroids to maintain an acceptable level of hemoglobin or platelets. The effects of the second line therapy are also not satisfactory and sometimes not available. The investigators aim to explore the efficacy and side-effect of tacrolimus for refractory autoimmune cytopenia.
Detailed Description
Tacrolimus binds FKBP12 with high affinity after entry into cytoplasm, suppresses calcineurin activity and prevents nuclear translocation of transcription factors such as NF-AT that are involved in IL-2 gene transcription. As a result, T-cell activation is inhibited with a subsequent reduction in the production of cytokines that include IL-2, TNF-α, IL-3, IL-4, IFN-γ, IL-6 and IL-10; B-cell activation, class-switching and immunoglobulin production are also attenuated. Reports on the use of tarcrolimus in the treatment of autoimmune cytopenia are anecdotal and describe therapy with a variety of drug dosages. The purpose of this study is to evaluate the effect of tacrolimus on patients with refractory autoimmune cytopenia, the side-effects will be documented and plasma concentration of tacrolimus will be monitor.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autoimmune Hemolytic Anemia, Pure Red Cell Aplasia, Evans Syndrome
Keywords
Tacrolimus, Refractory autoimmune cytopenia, Prospective study

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Efficiency of tacrolimus on autoimmune cytopenia
Arm Type
Experimental
Arm Description
A prospective research of the tacrolimus efficiency on refractory autoimmune cytopenia patients. Dosage: 1mg bid and tacrolimus trough targets were 5-10 ng/ml throughout the study. Medication time should last at least 6 months.
Intervention Type
Drug
Intervention Name(s)
Tacrolimus
Other Intervention Name(s)
tacrolimus capsule
Intervention Description
On refractory autoimmune cytopenia patients, tacrolimus was tried. Dosage: 1mg bid and tacrolimus trough targets were 5-10 ng/ml throughout the study
Primary Outcome Measure Information:
Title
Hemoglobin level
Description
Hemoglobin level in g/L
Time Frame
6 months
Title
Platelet count
Description
Platelet count in /L
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Hemoglobin level
Description
Hemoglobin level in g/L
Time Frame
2 years
Title
Platelet count
Description
Platelet count in /L
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Refractory autoimmune cytopenia, including autoimmune hemolytic anemia, pure red cell aplasia, Evans syndrome. 18-80 years old. No response or intolerant to first and second line therapies. ECOG Performance Status of 0-2 Written informed consent. Exclusion Criteria: Other diseases which might cause hematological abnormalities. Response and well tolerate to first or second line therapy. Patients who are under 18-year-old or over 80-year-old. Pregnant or lactating. Patients unwilling to or unable to comply with the protocol.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ruoxi Zhang, M.D.
Phone
+86 18510064839
Email
rx_zh15@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bing Hang, PhD
Organizational Affiliation
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
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ruoxi Zhang, MD
Phone
+86 18510064839
Email
rx_zh15@163.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
28566017
Citation
Li Y, Feng X. Efficacy and safety of tacrolimus in systemic lupus erythematosus patients with refractory thrombocytopenia: a retrospective study. Lupus. 2018 Jan;27(1):60-65. doi: 10.1177/0961203317711011. Epub 2017 May 31.
Results Reference
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PubMed Identifier
25209619
Citation
Tabchi S, Hanna C, Kourie HR, Aftimos P, El Osta L, Ghosn M. Successful treatment of Evans syndrome with Tacrolimus. Invest New Drugs. 2015 Feb;33(1):254-6. doi: 10.1007/s10637-014-0155-9. Epub 2014 Sep 12. No abstract available.
Results Reference
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Tacrolimus Treatment for Refractory Autoimmune Cytopenia

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