Study to asses if the immunoglobulin product for subcutaneous use in combination with Hyaluronidase has a positive effect on your disease, and if it safe to use. The study will also assess if the intravenous immunoglobulin product has a positive effect and is safe to use.
- Conditions
- Chronic inflammatory demyelinating polyradiculoneuropathyMedDRA version: 21.1Level: PTClassification code 10057645Term: Chronic inflammatory demyelinating polyradiculoneuropathySystem Organ Class: 10029205 - Nervous system disordersTherapeutic area: Diseases [C] - Nervous System Diseases [C10]
- Registration Number
- EUCTR2014-005496-87-GR
- Lead Sponsor
- Baxalta Innovations GmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 132
1. Males or females of age =18 years old at the time of screening.
2. Subject has a documented diagnosis of definite or probable CIDP (focal atypical CIDP and pure sensory atypical CIDP will be excluded).
3. Subject has responded to IgG treatment in the past, (partial or complete resolution of neurological symptoms and deficits), and must currently be on stable doses of IGIV treatment within the dose range equivalent to a cumulative monthly dose of 0.4 to 2.4 g/kg BW (inclusive) administered intravenously for at least 3 months prior to screening. The dosing interval of IGIV treatment must be between 2 to 6 weeks (inclusive).
4. INCAT disability score between 0 to 7 (inclusive). Subjects with INCAT scores of 0, 1 (whether from upper or lower extremities), or 2 (if at least 1 point is from an upper extremity) at screening and/or baseline will be required to have a history of significant disability as defined by an INCAT disability score of 2 (must be exclusively from the lower extremities) or greater within 24 months prior to screening.
5. If female of childbearing potential, the subject must have a negative pregnancy test at screening and agree to employ a highly effective contraceptive measure throughout the course of the study and for at least 30 days after the last administration of investigational product.
6. Subject is willing and able to sign an Informed Consent Form (ICF).
7. Subject is willing and able to comply with the requirements of the protocol.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 110
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 20
1.Subjects with focal atypical CIDP or pure sensory atypical CIDP.
2. Any neuropathy of other causes, including:
a. Hereditary demyelinating neuropathies, such as hereditary sensory
and motor neuropathy (Charcot-Marie-Tooth [CMT] disease), and
hereditary sensory and autonomic neuropathies.
b. Neuropathies secondary to infections, disorders, or systemic diseases
such as Borrelia burgdorferi infection (Lyme disease), diphtheria,
systemic lupus erythematosus, POEMS (polyneuropathy, organomegaly,
endocrinopathy, M-protein, and skin changes) syndrome, osteosclerotic
myeloma, diabetic and non-diabetic lumbosacral radiculoplexus
neuropathy, lymphoma, and amyloidosis
c. Multifocal acquired demyelinating sensory and motor neuropathy
(MADSAM)
d. Multifocal motor neuropathy
e. Drug-, biologic-, chemotherapy-, or toxin-induced peripheral
neuropathy
3. Immunoglobulin M (IgM) paraproteinemia, including IgM monoclonal
gammopathy with high titer antibodies to myelin-associated
glycoprotein.
4. Presence of prominent sphincter disturbance.
5. Any central demyelinating disorders such as multiple sclerosis.
6. Any chronic or debilitating disease, or central nervous disorder that
causes neurological symptoms or may interfere with assessment of CIDP
or outcome measures, including (but not limited to) arthritis, stroke, and
Parkinson's disease and diabetic peripheral neuropathy.
7. The subject has received or is currently receiving treatment with
immunomodulatory/immunosuppressive agents within 6 months prior to
screening.
8. The subject has received or is currently receiving treatment with any
corticosteroids dose within 8 weeks prior to screening, regardless of
indication.
9. The subject has undergone plasma exchange within 3 months prior to
screening.
10. The subject has any disorder or condition that in the investigator's
judgment may impede the subject's participation in the study, pose
increased risk to the subject, or confound the results of the study.
11. The subject is nursing or intends to begin nursing during the course
of the study.
12. Subjects with acquired or inherited thrombophilic disorders. These
will include the specific types of acquired or inherited thrombophilic
disorders that could put subjects at risk of developing thrombotic
events.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method