A Pilot Trial To Assess The Feasibility And Efficacy Of SCIG In Patients With MG Exacerbation (SCIG-MG) (SCIG-MG)

A Pilot Trial To Assess The Feasibility And Efficacy Of Subcutaneous Immunoglobulin In Patients With Myasthenia Gravis Exacerbation

This is a prospective open-label, uncontrolled, single-blind, pilot clinical trial.

The primary objective is to assess the efficacy, safety, feasibility and tolerability of SCIG in patients with worsening MG.

Participants with moderate worsening of MG symptoms (MGFA Class II and III) who are considered to be appropriate for immunoglobulin therapy will be screened for the study by the treating neurologist.

Patients will be receive 2gm/kg (150gm for a 75kg patient) of 20% SCIG (Hizentra) infused over 4 weeks in a dose escalating manner.

Additionally, this study will be assessing the feasibility of employing SCIG as an alternative therapy to IVIG in patients with MG exacerbation. The cost-effectiveness of SCIG versus IVIG will be evaluated, and the impact of SCIG therapy will be assessed from both a health-resource perspective and from a patient perspective.

Study Overview

• Status: Completed
• Conditions: Myasthenia Gravis
• Intervention / Treatment: Drug: Human normal immunoglobulin G (IgG)

Detailed Description

This is a prospective open-label, uncontrolled, single-blind, pilot clinical trial.

The primary objective is to assess the efficacy, safety, feasibility and tolerability of SCIG in patients with worsening MG.

Study Rationale and Significance

Subcutaneous immunoglobulin (SCIG) is a novel form of immune therapy for neuromuscular diseases and may offer several advantages over intravenous immunoglobulin (IVIG).

Although no large-scale studies have been in conducted in MG patients, pilot studies with SCIG in multifocal motor neuropathy indicate that it may be a feasible, effective and safe alternative to IVIG in a condition, which like MG, shows excellent response to IVIG infusion.

Patients are able to tolerate it better and have improved quality of life due to added flexibility to the treatment schedule. SCIG is also potentially less expensive than IVIG since the costs associated with inpatient treatment as well as nursing support are saved.

SCIG also has the potential to be more effective and durable since the serum levels of immunoglobulin show a more sustained increase compared to IVIG. A drawback associated with SCIG is the small amount of immunoglobulin that can be infused over a short period. As compared to IVIG where the usual dose (2gm/kg for neuromuscular diseases) can be infused over 2 - 5 days, the same dose of SCIG would require 3 - 4 weeks to be administered with the currently available formulations. This may mean a delayed onset of peak-dose effect and SCIG may not be feasible for MG patients who are rapidly worsening or in MG crisis.

Nevertheless, SCIG may be an attractive option in a large subpopulation of MG patients who have mild to moderate disease exacerbations or who are on maintenance IVIG therapy provided its efficacy, tolerability and feasibility is determined in this patient population.

Methodology

Participants with moderate worsening of MG symptoms (MGFA Class II and III) who are considered to be appropriate for immunoglobulin therapy at the MG clinic at the University of Alberta will be screened for the study by the treating neurologist.

Patients will be receive 2gm/kg (150gm for a 75kg patient) of 20% SCIG (Hizentra) infused over 4 weeks in a dose escalating manner. Participants will undergo infusions two to four times a week, depending on their tolerance, beginning with a dose of 10 ml per site at four injection sites, increasing by 5 ml per week for a total of 25 ml per site at four injection sites after four weeks.

The dose is flexible and will vary based on the patient's tolerance to the medication and the total amount of medication the patient will be receiving based on their body weight. The initial (one or two) doses will be infused within the medical outpatient facility at the University of Alberta Hospital. This will allow for the observation of any infusion reactions and will also serve as nurse-provided self- infusion training sessions for patients.

Participants will be assessed weekly for symptomatic change and reports of satisfaction and quality of life. The primary outcome variable is the change in the Quantitative Myasthenia Gravis (QMG) Score for Disease Severity from baseline to day 42 (6 weeks). A change of 3.5 points will be considered to be clinically significant.

Safety and pharmacokinetic assessments of SCIG will be performed weekly throughout the study.

Additionally, this study will be assessing the feasibility of employing SCIG as an alternative therapy to IVIG in patients with MG exacerbation. The cost-effectiveness of SCIG versus IVIG will be evaluated, and the impact of SCIG therapy will be assessed from both a health-resource perspective and from a patient perspective.

The practicality of using SCIG in patients with MG will be determined by documenting the number of patients who are able to be trained for self- administration of SCIG, and by the patients' self-reported satisfaction with SCIG treatment.

The speed of SCIG treatment onset will also be assessed and compared to IVIG treatment onset. All of these described measures will be used to determine the feasibility and practicality of using SCIG in patients with MG exacerbation and its impact on the healthcare system.

• Study Type: Interventional
• Enrollment (Actual): 26
• Phase: Phase 3

Contacts and Locations

• Study Contact: Name: Derrick G Blackmore, B.Sc; Phone Number: 780-407-3367; Email: dblackmo@ualberta.ca
• Study Contact Backup: Name: Ashley K Mallon, LPN; Phone Number: 780-407-6582; Email: akmallon@ualberta.ca

Study Locations

• Canada
  • Alberta
    • Edmonton, Alberta, Canada, T6G 2B7
      • University of Alberta
  • British Columbia
    • Vancouver, British Columbia, Canada, V5Z 1M9
      • Vancouver General Hospital - Gordon & Leslie Diamond Health Care Centre

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 80 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Patients between18 to 80 years of age, diagnosed with MG (see below) who have worsening myasthenic symptoms - (defined as increasing diplopia, ptosis, dysarthria, dysphagia, difficulty chewing, or limb weakness severe enough to warrant immunoglobulin therapy.

• MG diagnosis will be based upon the clinical evaluation by a neuromuscular expert and meeting any two of the following supportive criteria:

  1. Abnormal Tensilon test
  2. Abnormal repetitive nerve stimulation studies
  3. Abnormal single fiber electromyography (EMG)
  4. Increased serum acetylcholine receptor or anti-MuSK antibodies
  5. Prior response to immunotherapy

Exclusion Criteria:

1. Respiratory distress requiring ICU admission or a vital capacity <1 L
2. Severe swallowing difficulties with a high risk of aspiration
3. Change in corticosteroid dosage in the 4 weeks prior to screening
4. Known immunoglobulin A (IgA) deficiency
5. Pregnant or breast feeding women
6. Active renal or hepatic insufficiency, clinically significant cardiac disease
7. Patients with worsening weakness associated with an infectious process
8. Previous lack of responsiveness to IVIG
9. History of previous MG crises

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

Experimental: SC Treatment Period; Participants will receive 2gm/kg of Human normal immunoglobulin G (IgG) infused over 4 weeks in a dose escalating manner as follows: 1st week: 2-3 SCIG infusions of 10ml per site at four sites (total dose 16 to 24g)*; 2nd week: 2-3 SCIG infusions of 15ml per site at four sites (total dose 24 to 36g)*; 3rd week: 2-4 SCIG infusions of 20ml per site at four sites (total dose 32 to 64g)*; 4th week: 2-4 SCIG infusions of 25ml per site at four sites (total dose 40 to 80g)*Doses indicated are study recommended. Doses may be adjusted depending on tolerance and total dose required by the patient.

Drug: Human normal immunoglobulin G (IgG); Study medication is available in the following forms: 5 mL (1 g IgG) in a 5 mL infusion bottle, 10 mL (2 g IgG) in a 10 mL infusion bottle, 20 mL (4 g IgG) in a 20 mL infusion bottle, 50 mL (10 g IgG) in a 50 mL infusion bottle. Patients will be receiving 2gm/kg (150gm for a 75kg patient) of 20% SCIG (Hizentra) infused over four weeks in a dose escalating manner.; Other Names: Hizentra®

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Quantitative Myasthenia Gravis Score (QMGS) from baseline to day 42 after treatment.	QMGS is a validated clinical measure of myasthenia gravis ranging from 0 points (no myasthenic weakness) to a maximum of 39 points, with a defined change of 3.4 units required for clinical significance.	Baseline - Day 42

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Quality of life will be assessed through the Quality of Life (QOL) score, a qualitative questionnaire.		Baseline - Day 42
Change in Manual Muscle Testing (MMT) score from baseline to day 42 after treatment.	MMT is a validated clinical measure of myasthenia gravis ranging from 0 points (no myasthenic weakness) to a maximum of 128 points, with a defined change of 25% from baseline required for clinical significance.	Baseline - Day 42
Adverse events related to SCIG infusions will be recorded if/when they occur.		Baseline - Day 42
Patient satisfaction with the treatment modality will be assessed using a questionnaire.	TQSM: Treatment Satisfaction Questionnaire for Medication. An 11 question ordinal scale measuring responses from "Extremely satisfied" to "Extremely dissatisfied" over a 7 item option list. Questions cover four domains, corresponding to distinct aspects related to the satisfaction of patients with their treatment (Effectiveness; Side effects; Convenience and Global satisfaction). A score can be obtained for each domain by summing of the corresponding items transformed on a 0-100 scale; higher values indicate higher satisfaction, better perceived effectiveness, lower burden associated to side-effects, better convenience	Day 42
Serious Adverse Events related to SCIG infusions will be recorded if/when they occur.		Baseline - Day 42
Proportion of participants successfully trained will be recorded indicating feasibility based on patient compliance.		Baseline - Week 2
Proportion of participants completing will be recorded indicating feasibility based on patient compliance.		Baseline - Day 42
Myasthenia Gravis (MG) Composite scores will be used to evaluate disease severity through a number of functional assessments, including muscle strength and ability to complete activities of daily living.		Baseline - Day 42

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Cost effectiveness of SCIG therapy will be calculated in comparison to standard IVIG therapy. This will indicate health economics.		Baseline - Day 42
Change in QOL 36 score from Baseline to day 42)	Change in Quality of Life (QOL) score from Baseline to day 42.	Baseline - Day 42
Time required for the treatments.	Average time in minutes required for each infusion session during study. Determined for each participant.	Baseline - Day 42
Preference for treatments (Treatment Satisfaction Questionnaire for Medication (TSQM).	11 item scale measuring treatment satisfaction for medication over 3 domains (Effectiveness, Side effects, Convenience, Global Satisfaction). Score from 10 to 43	Day 42
Intent to continue using SCIG if necessary (Via pt. interview)	Yes= will continue SCIG therapy, No= will not continue SCIG therapy.	Day 42
Proportion of participants successfully trained in self-administration of SCIG.	Proportion of participants who successfully trained in self-administration of SCIG expressed as a percentage (completed training/underwent training x 100).	Day 2, Day 3.
Proportion of participants completing the study.	Proportion of patients who completed the study expressed as a percentage (finished study/started study x 100).	Day 42
Infusion nurse's assessment of this participant population's ability to use this treatment modality (Written impression)	Qualitative measure. Narrative reflecting the infusion nurse's overall impression of target population's ability to employ SCIG within the parameters defined by the study. (data is a written narrative. By definition, this has no units nor is it collected by any instrument (questionnaire, scale parameter ect.) ie. QUALITATIVE data)	Day 42
Speed of treatment onset of SCIG.	The number of days between prescription of SCIG treatment and infusion of first dose.	Day 1
Speed of treatment onset of IVIG.	The number of days between prescription of IVIG treatment and infusion of first dose, for any study participant who has received IVIG treatments in the past. This interval will be determined for all available previous IVIG infusions for each patient.	Day 1

Collaborators and Investigators

• Sponsor: University of Alberta
• Collaborators: CSL Behring
• Investigators: Principal Investigator: Zaeem A Siddiqi, MD, PhD, University of Alberta

Study record dates

Study Major Dates

• Study Start: October 1, 2014
• Primary Completion (Actual): October 21, 2022
• Study Completion (Actual): October 21, 2022

Study Registration Dates

• First Submitted: April 20, 2015
• First Submitted That Met QC Criteria: May 16, 2016
• First Posted (Estimate): May 17, 2016

Study Record Updates

• Last Update Posted (Estimate): February 21, 2023
• Last Update Submitted That Met QC Criteria: February 17, 2023
• Last Verified: February 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Nervous System Diseases; Immune System Diseases; Neoplasms; Autoimmune Diseases of the Nervous System; Autoimmune Diseases; Neoplasms by Site; Neuromuscular Diseases; Neurodegenerative Diseases; Nervous System Neoplasms; Paraneoplastic Syndromes, Nervous System; Paraneoplastic Syndromes; Neuromuscular Junction Diseases; Myasthenia Gravis; Physiological Effects of Drugs; Immunologic Factors; Antibodies; Immunoglobulins; Immunoglobulins, Intravenous; Immunoglobulin G
• Other Study ID Numbers: ZS2013-01

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No