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An Open Label Study of the Effects of Eculizumab in CD59 Deficiency

Primary Purpose

Chronic Hemolysis

Status
Unknown status
Phase
Phase 1
Locations
Israel
Study Type
Interventional
Intervention
Eculizumab
Sponsored by
Hadassah Medical Organization
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Hemolysis

Eligibility Criteria

2 Months - 70 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • CD59 deficiency

Exclusion Criteria:

  • recent exposure to meningococcal infections

Sites / Locations

  • Hadassah Medical CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Eculizumab

Arm Description

Eculizumab will be administrated according to known protocols.

Outcomes

Primary Outcome Measures

Whether Eculizumab reduces chronic hemolysis
The primary objectives of this study are to determine: Whether Eculizumab reduces chronic hemolysis as judged by LDH levels, and haptoglobin, and level of hemoglobin.
Steroid and iv IgG cumulative dosage
Cumulative steroid and IgG dosage before and after treatment
Safety.
Whether the subjects develop known or possible related side effect to the treatment. The number of participants that develop adverse effects will be determined. reports from parents will be taken avery other week and documented clini or hospital visits will be included.
Whether Eculizumab ameliorates the neurological status compared to one month before treatment
The neurological status in the last month prior to treatment will be determined followed by neurological staus examination every two weeks.

Secondary Outcome Measures

Whether eculizumab maintains or improves limbs motion
Whether there is a neurological amelioration
function and quality of life as measured by a variety of established disability scales.
we will be using evry other week parents report of his clinical condition. We will use modified SF36 and local questionairre.
The severity of an individual attack and the degree of recovery.
Levels of membrane attack complex
This will be measured using flow cytometry for the presence of membrane attack complex on neutrophild and res blood cells.

Full Information

First Posted
February 23, 2012
Last Updated
April 17, 2012
Sponsor
Hadassah Medical Organization
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1. Study Identification

Unique Protocol Identification Number
NCT01579838
Brief Title
An Open Label Study of the Effects of Eculizumab in CD59 Deficiency
Official Title
An Open Label Study of the Effects of Eculizumab in CD59 Deficiency
Study Type
Interventional

2. Study Status

Record Verification Date
April 2012
Overall Recruitment Status
Unknown status
Study Start Date
February 2012 (undefined)
Primary Completion Date
March 2013 (Anticipated)
Study Completion Date
March 2013 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hadassah Medical Organization

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators have identified patients with CD59 deficiency that suffers from chronic hemolysis and peripheral demyelinating disease. It was shown that complement terminal pathway can cause inflammation in the peripheral nervous system. Complement can greatly increase the immune attack in the nerves. Eculizumab has already been shown to be effective in a rare blood disorder known as paroxysmal nocturnal hemoglobinuria (PNH). Attacks of PNH are also mediated through complement. Therefore, the investigators of this study are investigating whether by 'turning off' complement in CD59 deficiency, further attacks of hemolysis and nerve injury can be avoided and whether the neurological status will ameliorate.
Detailed Description
It has been shown in some scientific studies that lack of CD59 in the context of the disease paroxysmal nocturnal hemoglobinuria (PNH)leads to chronic hemolysis. The investigators have identified patients wirh CD59 deficiency that suffers from chronic hemolysis and demyelinating disease. It was shown that complement terminal pathway can cause cause inflammation in nervous system. Complement can greatly increase the immune attack in the nerves. Eculizumab has already been shown to be effective in a rare blood disorder known as PNH. Attacks of PNH are also mediated through complement. Therefore, the investigators of this study are investigating whether by 'turning off' complement in CD59 deficiency, further attacks of hemolysis and nerve injury can be avoided. The primary (most important) objectives of this study are to determine: Whether Eculizumab ameliorate the neurological condition documented in the last month before treatment and whether it reduces the relapse frequency in patients with relapsing chronic inflammatory demyilinating polyneuropathy. The number of attacks during the one year treatment period will be compared to the number of attacks that occurred prior to initiation of eculizumab treatment. For patients with more than 2 year disease duration, the average number of attacks in the preceding 2 years will be calculated. For patients with less than 2 years disease duration the number of attacks in the preceding year will be used. Whether Eculizumab reduces chronic hemolysis as judged by LDH levels, and haptoglobin, and level of hemoglobin. the same for corticosteroids and or I.V. IgG consumption before and after treatment with eculizumab. The safety profile of eculizumab in patients with CD59 deficiency will be determined by parents report evry other week, documentation of clinic referral and hospitalizations. The number of participants with advers events will be determined. The secondary objectives are to determine: Whether eculizumab maintains or improves limbs motion, function and quality of life as measured by a variety of established disability scales like the modified SF36 and like a questionaire developed for this age group. The investigators will also assess the severity of an individual attack and the degree of recovery. How the drug behaves in the patient's blood by measuring the presence of membrane attack complex on neutrophils and red blood cells.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Hemolysis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
5 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Eculizumab
Arm Type
Experimental
Arm Description
Eculizumab will be administrated according to known protocols.
Intervention Type
Drug
Intervention Name(s)
Eculizumab
Other Intervention Name(s)
Soliris
Intervention Description
PNH and or atypical TTP classical protocols
Primary Outcome Measure Information:
Title
Whether Eculizumab reduces chronic hemolysis
Description
The primary objectives of this study are to determine: Whether Eculizumab reduces chronic hemolysis as judged by LDH levels, and haptoglobin, and level of hemoglobin.
Time Frame
8 months
Title
Steroid and iv IgG cumulative dosage
Description
Cumulative steroid and IgG dosage before and after treatment
Time Frame
8 months
Title
Safety.
Description
Whether the subjects develop known or possible related side effect to the treatment. The number of participants that develop adverse effects will be determined. reports from parents will be taken avery other week and documented clini or hospital visits will be included.
Time Frame
8 months
Title
Whether Eculizumab ameliorates the neurological status compared to one month before treatment
Description
The neurological status in the last month prior to treatment will be determined followed by neurological staus examination every two weeks.
Time Frame
8 months
Secondary Outcome Measure Information:
Title
Whether eculizumab maintains or improves limbs motion
Description
Whether there is a neurological amelioration
Time Frame
8 months
Title
function and quality of life as measured by a variety of established disability scales.
Description
we will be using evry other week parents report of his clinical condition. We will use modified SF36 and local questionairre.
Time Frame
8 months
Title
The severity of an individual attack and the degree of recovery.
Time Frame
8 months
Title
Levels of membrane attack complex
Description
This will be measured using flow cytometry for the presence of membrane attack complex on neutrophild and res blood cells.
Time Frame
8 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Months
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: CD59 deficiency Exclusion Criteria: recent exposure to meningococcal infections
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dror Mevorach, MD
Email
mevorachd@hadassah.org.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dror Mevorach, MD
Organizational Affiliation
hmo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hadassah Medical Center
City
Jerusalem
ZIP/Postal Code
91120
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dror Mevorach, MD
Phone
972-2- 6777317
Email
mevorachd@hadassah.org.il
First Name & Middle Initial & Last Name & Degree
Dror Mevorach, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
27568864
Citation
Mevorach D, Reiner I, Grau A, Ilan U, Berkun Y, Ta-Shma A, Elpeleg O, Shorer Z, Edvardson S, Tabib A. Therapy with eculizumab for patients with CD59 p.Cys89Tyr mutation. Ann Neurol. 2016 Nov;80(5):708-717. doi: 10.1002/ana.24770. Epub 2016 Sep 19.
Results Reference
derived

Learn more about this trial

An Open Label Study of the Effects of Eculizumab in CD59 Deficiency

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