Tacrolimus Combined With Low-dose Prednisone for Treatment of Myasthenia Gravis

Myasthenia Gravis Clinical Trial

Official title:

Effectiveness and Safety of Tacrolimus Combined With Low-dose Prednisone for Treatment of Myasthenia Gravis: A Real-world Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04768465
• Other study ID #: 1.0
• Status: Recruiting
• Start date: January 1, 2021
• Est. completion date: October 31, 2024

Study information

• Verified date: February 2021
• Source: Da, Yuwei, M.D.
• Contact: Yuwei Da, M.D.
• Phone: 00-86-010-83198493
• Email: dayuwei1000[@]163.com
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

This study is designed to evaluate the effectiveness and safety of tacrolimus combined with low-dose prednisone in the management of myasthenia gravis patients, compared to tacrolimus as initial immune monotherapy.

Description:

This is a single center, observational real-world study recruiting myasthenia gravis patients from Neurology Departments of Xuanwu Hospital, aiming to compare effectiveness and safety of 2 different inmunotherapy for MG. The study plans to recruit 160 MG participants and divides into 2 treatment groups according to physician's judgment and preferences of patients, one is combined immunotherapy group in which tacrolimus added with low-dose prednisone (0.25mg/kg/d), and the other is tacrolimus monotherapy group. Both groups can be treated with pyridostigmine to relieve symptoms. Patients are followed up at 1, 3 and 6 month after treatment initiation to assess the efficacy of both regimen. The primary outcome is the change of MG-ADL scores. Also, liver and renal functions are tested to monitor any side effects. Patients' clinical records are uploaded to an online database.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 160
• Est. completion date: October 31, 2024
• Est. primary completion date: December 31, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age =18
• Clinical Diagnosis of MG is confirmed based on typical clinical features of

fluctuating muscle weakness, with at least 1 of the following supporting evidence:

1. positive clinical response to acetylcholinesterase inhibitor

2. positive AchR-Ab or MuSK-Ab testing

3. decrement >10% in repetitive nerve stimulations study (RNS) or increased jitter on single-fibre electromyography (SFEMG)

• MGFA clinical classification: I - IV
• Baseline MG-ADL = 3
• Disease course from onset to enrollment = 12 months
• Cooperation to followup
• Written informed consent

Exclusion Criteria:

• Initiation of immunosuppressant for MG prior to screening, including Prednisone, Methylprednisolone, Azathioprine, Methotrexate, Cyclosporine A, Mycophenolate Mofetil, Tacrolimus and Cyclophosphamide
• Treatment of immunosuppressant for other concomitant disease 6 months prior to recruitment
• Rapid immunosuppressive treatments like Intravenous immunoglobulin or plasma exchange 1 month prior to recruitment
• Thymectomy within 3 months prior to Screening
• Concomitant chronic degenerative, psychiatric, or neurologic disorder that can cause weakness or fatigue
• Consciousness, dementia or schizophrenia
• Pregnancy or lactation, unwillingness to avoid pregnancy
• Uncontrolled hypertension or diabetes, Liver or kidney dysfunction, Cataract, Severe osteoporosis, Femoral head necrosis; Hyperkalemia, HIV, Acute or chronic infection
• Other conditions that would preclude participation

Related Conditions & MeSH terms

• Muscle Weakness
• Myasthenia Gravis

Intervention

Drug:
• Pyridostigmine, Prednisone, Tacrolimus
Dose of tacrolimus should be initiated based on CYP3A5*3 polymorphism and adjusted to achieve blood trough concentration of 4.8-10.0 ng/ml. Prednisone is administrated with an initial dose of 0.25mg/kg/d and started to tamper with the achievement of MMS or the presence of any intolerable side effects. The rate of tampering is considered by the physician, usually no more than 5mg/month. If the participants failed to maintain MMS, dose of prednisone should be increased 5mg/week to 0.25mg/kg/d and maintained until MMS reached again. After MMS sustained for 1 month, prednisone dose would be tapered again with 2.5mg/month. Calcium and potassium supplements and gastric mucosa protectors could be addressed to avoid any adverse effects of prednisone. Treatment regimens are determined based on the physician's judgment and preferences of the patients. This study was observational and do not change the clinical course of patients.
• Pyridostigmine, Tacrolimus
Dose of tacrolimus should be initiated based on CYP3A5*3 polymorphism and adjusted to achieve blood trough concentration of 4.8-10.0 ng/ml. Treatment regimens are determined based on the physician's judgment and preferences of the patients. This study was observational and do not change the clinical course of patients.

Locations

Country	Name	City	State
China	Yuwei Da	Beijing	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Da, Yuwei, M.D.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change of MG-specific Activities of Daily Living scale (MG-ADL) from Baseline	The MG-ADL is an 8-item scale to assess symptoms of myasthenia gravis patients obtained by summing the responses to each individual item (Grades: 0,1,2,3). The score ranges from 0 to 24.	Baseline, 1 month, 3 months, 6 months
Secondary	Time to achievement of minimal manifestations (MMS) or better	The time duration from treatment initiation to the achievement of MMS or better. Clinical statuses of patients are assessed and categorized according to Myasthenia Gravis Foundation of America (MGFA) post-intervention status (PIS). MM or better includes Minimal Manifestation (MM), Pharmacologic Remission (PR) or Complete Remission (CR).	From Baseline to 6 months
Secondary	Time to achievement of Patient-Acceptable Symptom States	The Patient-Acceptable Symptom States question is a simple yes or no query that asked: "Considering all the ways you are affected by Myasthenia, if you had to stay in your current state for the next month, would you say that your current disease state status is satisfactory?" This question reflects the patients assessment of their own health.	From Baseline to 6 months
Secondary	Change of Quantitative Myasthenia Gravis (QMG) Scores from Baseline	The QMG is a 13-item scale which measures ocular, bulbar, limb function and respiratory function. The total score ranges from 0 (no myasthenic findings) to 39 (maximal myasthenic deficits) obtained by summing the responses to each individual item (None=0, Mild=1, Moderate=2, Severe=3).	Baseline, 1 month, 3 months, 6 months
Secondary	Change of Myasthenia Gravis Quantity-of-Life Scale (MG-QoL15) from Baseline	The MG-QOL15 is helpful in informing the clinician about the patient's perception of the extent of and dissatisfaction with myasthenia gravis (MG)-related dysfunction. MG-QOL15 evaluates patients' aspects about physical status, social adaptation and mental well-being.	Baseline, 1 month, 3 months, 6 months
Secondary	Changes of MG-ADL subscores from baseline	Subscores of ADL items can reflect patients' assessment about different MG-related dysfunctions, including ptosis, diplopia, talking, chewing, swallowing, breathing and limbs function.	Baseline, 1 month, 3 months, 6 months
Secondary	Serum IL-2 level	Tacrolimus exerts its immunosuppressive effect by inhibiting the early phase gene expression during T-cell activation, including the pro-inflammation IL-2 gene. Thus serum IL-2 is tested as a target of tacrolimus and also a marker of in vivo auto-immune status after treatment.	Baseline, 1 month, 3 months, 6 months
Secondary	Treatment Failure	Treatment failure is defined as discontinuation of tacrolimus therapy in patients who failed to achieve MMS or better or suffered from exacerbations (MG-ADL or QMG scores increase 50%) or myasthenia crisis.	Baseline to 6 months
Secondary	Withdrawal	Participants quit the clinical trial for any reason including unsatisfied response, economic burden or poor compliance to treatment protocol. Patients may quit at any time they want.	Baseline to 6 months