Phase III Study of KD-380

JRCT ID: jRCT2051240028

Registered date:09/05/2024

Basic Information

• Recruitment status: Recruiting
• Health condition(s) or Problem(s) studied: Chronic inflammatory demyelinating polyradiculoneuritis and multifocal motor neuropathy
• Date of first enrollment: 10/05/2024
• Target sample size: 33
• Study type: Interventional

Intervention(s)

Patients with CIDP/MMN
1. Acute treatment
GGL will be administered as human immunoglobulin at a dose of 400 mg (4 mL)/kg body weight intravenously for 5 consecutive days. If the patient meets the criteria* for the second course of treatment, GGL will be administered as human immunoglobulin at a dose of 400 mg (4 mL)/kg body weight intravenously for 5 consecutive days at 4 weeks after the start of treatment.
*Second course administration criteria: INCAT total score (patients with CIDP) or MRC total score (patients with MMN) unchanged or worsened by at least 1 point (1 step) compared to before the start of treatment at 4 weeks after the start of treatment. The INCAT score is evaluated with the adjusted INCAT score.
2. Maintenance therapy
GGL will be administered as human immunoglobulin at a dose of 1000 mg (10 mL)/kg body weight intravenously for 1 day or 500 mg (5 mL)/kg body weight intravenously for 2 consecutive days. Thereafter, the same conditions are administered every 3 weeks.

Outcome(s)

Primary Outcome

Patients with CIDP
- Percentage improvement in adjusted INCAT score in the first course of acute treatment
- Percentage worsening of adjusted INCAT score during the first phase of maintenance therapy
Patients with MMN
Medical Research Council (MRC) total score in the first course of acute treatment and first phase of maintenance therapy and amount of change in score from baseline.

Key inclusion & exclusion criteria

• Age minimum: >= 18age old
• Age maximum: Not applicable
• Gender: Both

Include criteria

(1) Patients aged 18 years or older at the time of informed consent
(2) CIDP patients only: Patients diagnosed with CIDP as defined in the 2021 EAN/PNS Guideline (excluding patients with possible CIDP)
(3) MMN patients only: Patients diagnosed with MMN as defined in the 2010 EFNS/PNS Guideline (excluding patients with possible MMN)
(4) Patients with progressive, recurrent CIDP (acute treatment cohort) or MMN (regardless of history of treatment with IVIg/SCIg)
(5) Patients with CIDP (maintenance therapy cohort): Patients on IVIg/SCIg maintenance therapy who have responded to IgG administration (Patients receiving IVIg 0.4 to 1.2 g/kg every 2 to 6 weeks for the past 12 weeks from the time of eligibility confirmation or SCIg 80 to 480 mg/kg every 1 to 2 weeks for the past 12 weeks from the time of eligibility confirmation).
(6) Patients with CIDP (acute treatment cohort): Patients with an INCAT (Inflammatory Neuropathy Cause and Treatment) score between 2 and 9 points of disability at the time of eligibility confirmation (but with a lower limb disability score of 2 or more, if the upper limb disability score is 1).
(7)Patients with CIDP (maintenance therapy cohort): Patients with an INCAT score between 0 and 7 points at the time of eligibility confirmation and a previous disability with an INCAT score between 2 and 9 points (but with a lower limb disability score of 2 or more, if the upper limb disability score is 1).
(8) In the case of using therapeutic agents * for CIDP and MMN within 30 days prior to eligibility confirmation, the patients who continue without adding and increasing dosage and require treatment with this investigational products.
*Steroids, azathioprine, tacrolimus, cyclosporine, cyclophosphamide, methotrexate, mycophenolate mofetil, fingolimod, eculizumab, etc.

Exclude criteria

Patients with CIDP
(1) Patients with sensory CIDP
(2) Patients with autoimmune nodopathy
(3) Patients with autoimmune inflammatory neuropathy such as multifocal motor neuropathy (MMN), Guillain-Barre syndrome, POEMS syndrome, IgM paraproteinemia including MAG antibody-associated neuropathy
(4) Patients with hereditary neuropathy such as Charcot-Marie-Tooth disease , hereditary sensory and autonomic neuropathy (HSAN).
(5) Patients with neuropathy secondary to internal diseases such as diabetes mellitus, cancer, collagen disease, amyloidosis, or infection such as Borrelia burgdorferi infection (Lyme disease), diphtheria (Eligible if there is no diabetic neuropathy, HbA1c level is stable and blood glucose control can be maintained appropriately ).
(6) Patients with drugs, biological products, chemotherapy or toxicant induced neuropathy.
(7) Patients who received maintenance therapy with IVIg/SCIg for more than 52 weeks (maintenance therapy cohort only) (however, patients who received maintenance therapy with IVIg/SCIg for more than 52 weeks may also be enrolled if immunoglobulin administrations are considered necessary based on medical judgment).

Patients with MMN
(8) Patients with CIDP
(9) Patients with other neuromuscular diseases (e.g., hereditary motor neuropathy, motor neuron disease, neuromuscular junction disease, muscle disease, diabetes mellitus, cervical spondylosis, lumbar spondylosis, hereditary neuropathy with liability to pressure palsies , peripheral nerve tumor, vasculitic neuropathy, sarcoid neuropathy, etc.).

Patients with CIDP/MMN
(10) Patients with central demyelinating diseases such as multiple sclerosis.
(11) Patients with chronic illnesses or central nervous system disorders (e.g., stroke, Parkinson's disease, amyotrophic lateral sclerosis, etc.) that may cause neurological symptoms or signs or may affect treatment outcomes or evaluation.
(12) Patients who have an active malignancy requiring chemotherapy and/or radiation therapy, or have a medical history of malignancy and have been in complete remission for less than 2 years prior to eligibility confirmation. Exceptions to this exclusion criterion are appropriately treated basal cell or squamous cell carcinoma of the skin, intraepithelial carcinoma of the cervix, and stable prostate cancer not requiring treatment.
(13) For the most recent IVIg dose administered prior to eligibility confirmation, those who received 0.75-1.2 g/kg and less than 6 weeks, and those who received less than 0.75 g/kg and less than 3 weeks (excluding patients with CIDP (maintenance therapy cohort)).
(14) Patients who received SCIg in excess of 480 mg/kg as a single dose in the 4-5 weeks (22-35 days) prior to eligibility confirmation, patients who received SCIg in excess of 240 mg/kg as a single dose (480 mg/kg total) in the 3-5 weeks (15-35 days) prior to eligibility confirmation, patients who received SCIg in excess of 120 mg/kg as a single dose (480 mg/kg total) in the 2-5 weeks (8-35 days) prior to eligibility confirmation (but must not have received SCIg in the 1 week (1-7 days) prior to eligibility confirmation) (excluding patients with CIDP (maintenance therapy cohort)).
(15) Patients with heart failure, cardiomyopathy, severe arrhythmia requiring treatment, or ischemic heart disease.
(16) Patients who have a medical history of pulmonary embolism, deep vein thrombosis or thromboembolic event in the past 12 months from the time of eligibility confirmation.
(17) Patients with severe liver disease (alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 3 times the upper limit of reference (ULN)) or severe kidney disease (creatinine > 1.5 times the upper limit of reference).
(18) Patients with severe anemia that interferes with repeated blood sampling in the clinical trial or whose a hemoglobin (Hb) valuel < 10.0 g/dL at the time of eligibility confirmation.
(19) Patients with a medical history of hypersensitivity or adverse reactions such as urticaria, dyspnoea, severe headache, severe hypotension or anaphylaxis following administration of human blood products (IgG, albumin and other blood components).
(20) Patients who falls under any of the following:
a) Patients with IgA deficiency
b) Patients with anti-IgA antibodies
c) Patients with a medical history of hypersensitivity to IgA
(21) Patients with an abnormal laboratory value meets any of the following criteria at the time of eligibility confirmation.
a) Platelet count < 100,000/microL
b) Absolute neutrophil count (ANC) < 1000/microL
(22) Patients who are positive for human immunodeficiency virus (HIV) type 1/2 or hepatitis B/C virus at the time of eligibility confirmation.
(23) Patients who have received plasma exchange therapy within 3 months prior to eligibility confirmation.
(24) Patients who have increased the dosage and administration of the following therapeutic agents * or those who have added a therapeutic agents for 30 days prior to eligibility confirmation.
*Steroids, azathioprine, tacrolimus, cyclosporine, cyclophosphamide, methotrexate, mycophenolate mofetil, fingolimod, eclyzumab, etc.
(25) Patients who have been treated with rituximab during the 6 months prior to eligibility confirmation.
(26) Patients with any disability or medical condition that is judged by the principal investigator or subinvestigator to interfere with the patient's participation in the study, to pose a significant risk to the patient or to be confounding to the outcome of the study.
(27) Lactating women , pregnant women, women/men planning to become pregnant, or women/men who have no intention to use an effective contraceptive during this study.
(28) Patients who have participated in another study and received other investigational products or devices within 30 days prior to eligibility confirmation , or who are scheduled to participate in another study during the participation period in this study using other investigational products or devices.
(29) Patients who are family members of the principal investigator or the subinvestigator, or employees of this study site and the sponsor.
(30) Patients with a history of drug or alcohol abuse in the past 5 years from the time of eligibility confirmation.
(31) Patients who unable to understand or who are not willing to comply with this study.

Related Information

• Primary Sponsor: Shinmura Yasuhiko