An Open-label Study to Investigate the Clinical Efficacy of Different Dosing Regimens of Efgartigimod IV in Patients With Generalized Myasthenia Gravis
- Conditions
- Generalized Myasthenia Gravis
- Interventions
- Biological: Efgartigimod concentrate for solution for infusion 20 mg/mL
- Registration Number
- NCT04980495
- Lead Sponsor
- argenx
- Brief Summary
The purpose of this open-label study is to investigate the efficacy, safety, and tolerability of a continuous regimen of efgartigimod compared with a cyclic regimen in participants with Generalized Myasthenia Gravis (gMG).
Study details include:
The study duration will be up to 138 weeks (including screening and a safety follow-up of up to 9 weeks)
* Part A (regimen comparison period) - 21 weeks
* Part B (extension period) - up to 105 weeks
The visit frequency, including virtual visits, will be weekly through Week 21 and every 5 weeks for the remainder of the study.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 69
- Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.
- At least 18 years of age, at the time of signing the informed consent.
- Diagnosed with Generalized Myasthenia Gravis (gMG) with confirmed documentation and supported by a physical exam and confirmed seropositivity for anti-acetylcholine receptor antibodies (AChR-Abs).
- Meets the clinical criteria as defined by the Myasthenia Gravis Foundation of America (MGFA) class II, III, or IV
- Has an Myasthenia Gravis - Activities of Daily Living (MG-ADL) total score ≥5 at screening and the day 1 visit, with more than 50% of the score due to nonocular symptoms
- Concomitant gMG treatment is permitted. Permitted concomitant gMG treatment includes nonsteroidal immunosuppressive drugs (NSIDs), steroids, and/or acetylcholinesterase (AChE) inhibitors. If receiving corticosteroids and/or NSIDs, must be on a stable dose for at least 1 month before screening.
- Contraceptive use should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies and: Women of childbearing potential must have a negative serum pregnancy test at screening and a negative urine pregnancy test at baseline before investigational medicinal product (IMP) can be administered.
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Clinically significant uncontrolled active or chronic bacterial, viral, or fungal infection at screening
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A positive test for SARS-CoV-2 at screening
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Any other known autoimmune disease that, in the opinion of the investigator, would interfere with an accurate assessment of the clinical symptoms of gMG and/or put the participant at undue risk
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History of malignancy unless deemed cured by adequate treatment with no evidence of reoccurrence for ≥3 years before the first administration of the IMP. Participants with the following cancers can be included at any time, provided they are adequately treated at screening: Basal cell or squamous cell skin cancer; carcinoma in situ of the cervix; Carcinoma in situ of the breast; Incidental histological finding of prostate cancer (TNM stage T1a or T1b)
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Clinical evidence of other significant serious diseases, a recent (<3 months) major surgery, or any other condition that, in the opinion of the investigator, could confound the results of the study or put the participant at undue risk
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A thymectomy within 3 months of screening
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Pregnant or lactating females and those who intend to become pregnant during the study or within 90 days of the last dose of IMP
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Use of the following prior or concomitant therapies:
- intravenous immunoglobulin (IVIg) or subcutaneous immunoglobulin (SCIg) within 14 days of day 1
- Rituximab within 6 months of day 1
- Eculizumab within 1 month of day 1
- Other monoclonal antibodies (eg, adalimumab, tocilizumab, ixekizumab) within 5 half-lives of the monoclonal antibodies before day 1
- Use of any other investigational product within 3 months or 5 half-lives, whichever is longer, before day 1
- Receipt of a live or live-attenuated vaccines received within 4 weeks of screening. The receipt of any inactivated, subunit, polysaccharide, conjugate vaccine at any time before screening is not considered exclusionary.
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Previous participation in a clinical study or patient access program during which they were treated with efgartigimod
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Positive serum test at screening for an active viral infection with any of the following conditions: Hepatitis B virus (HBV) that is indictive of an acute or chronic infection; Hepatitis C virus (HCV) based on HCV antibody assay (unless associated with a negative HCV RNA test); HIV based on test results that are associated with an AIDS-defining condition or a CD4 count <200 cells/mm3
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Total IgG <6 g/L at screening
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Known hypersensitivity reaction to efgartigimod or any of its excipients
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The participant stands in any relationship of dependency with the sponsor.
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The participant has been institutionalized due to an official or judicial order.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description efgartigimod IV - II Efgartigimod concentrate for solution for infusion 20 mg/mL Patients receiving efgartigimod IV treatment (Cyclic regimen: efgartigimod 10 mg/kg q7d for a total of 4 infusions per TP for 2 TPs with a fixed 4-week IP between each TP) efgartigimod IV - I Efgartigimod concentrate for solution for infusion 20 mg/mL Patients receiving efgartigimod IV treatment (Continuous regimen: efgartigimod 10 mg/kg q2w)
- Primary Outcome Measures
Name Time Method Mean of the average Myasthenia Gravis - Activities of Daily Living (MG-ADL) total score change from baseline during the visit of week (W)1 through W21 by regimen arm. A higher total score indicates more impairment. 21 weeks
- Secondary Outcome Measures
Name Time Method Normalized area under the effect curve (AUEC) of MG-ADL total score improvement from baseline during following intervals: Day 1 through Week7, Week 7 through Week 14, Week 14 trough Week 21 and Week 7 through Week 21 21 weeks Incidence and severity of adverse events (AEs), serious adverse events (SAEs) and AEs of special interest (AESIs) 136 weeks Number of participants who have a ≥2, 3, 4, or 5 points improvement in MG-ADL total score from baseline. during the following 5 intervals: W1 through W7, W8 through W14, W15 through W21, W8 through W21 and W1 through W21. 21 weeks Number of participants who achieve minimal symptom expression (MSE), defined as a MG-ADL total score of 0 or 1 21 weeks Change from baseline in the Myasthenia Gravis - Activities of Daily Living (MG-ADL) total score over time. A higher total score indicates more impairment. 126 weeks Characterization of MG-ADL total score change from baseline during the following 5 intervals using mean and standard deviation: Week 1 through Week 7, Week 8 through Week 14, Week 15 through Week 21, Week 8 through Week 21 and Week 1 through Week 21. 21 weeks Percentage of participants who have a ≥2, 3, 4, or 5 points improvement in MG-ADL total score from baseline during the following 5 intervals: W1 through W7, W8 through W14, W15 through W21, W8 through W21 and W1 through W21. 21 weeks Percentage of participants who achieve minimal symptom expression (MSE), defined as a MG-ADL total score of 0 or 1 in the following 5 intervals: W1 though W7, W8 through W14, W15 through W21, W8 through W21 and W1 through W21. 21 weeks Incidence of serious adverse events (SAEs) and AEs of special interest (AESIs) 136 weeks Percentage of time, participants have a change in MG-ADL total score of at least 2 points from baseline during Week 4 through Week 21. 21 weeks
Trial Locations
- Locations (39)
Investigator Site 9 - 0010006
🇺🇸Boca Raton, Florida, United States
Investigator Site 17 - US0010012
🇺🇸Philadelphia, Pennsylvania, United States
Investigator Site 10 - US0010007
🇺🇸Carlsbad, California, United States
Investigator Site 12 - US0010004
🇺🇸Kansas City, Kansas, United States
Investigator Site 6 - US0010008
🇺🇸Meadows, Illinois, United States
Investigator Site 7 - US0010001
🇺🇸Orange, California, United States
Investigator Site 16 - US0010009
🇺🇸Augusta, Georgia, United States
Investigator Site 11 - US0010011
🇺🇸Austin, Texas, United States
Investigator Site 14 - US0010010
🇺🇸Richmond, Virginia, United States
Investigator Site 36 - DE0490002
🇩🇪Bochum, Germany
Investigator Site 26 - AT0430002
🇦🇹Innsbruck, Austria
Investigator Site 27 - AT0430001
🇦🇹Wien, Austria
Investigator Site 28 - BE0320001
🇧🇪Leuven, Belgium
Investigator Site 29 - CA0019003
🇨🇦London, Canada
Investigator Site 20 - FR0330001
🇫🇷Marseille, France
Investigator Site 25 - FR0330003
🇫🇷Nice, France
Investigator Site 2 - GEO9950002
🇬🇪Tbilisi, Georgia
Investigator site 38 - FR0330002
🇫🇷Paris, France
Investigator Site 33 - DE0490004
🇩🇪Berlin, Germany
Investigator Site 3 - GEO9950003
🇬🇪Tbilisi, Georgia
Investigator Site 35 - NL0310001
🇳🇱Amsterdam, Netherlands
Investigator Site 21 - IT0390002
🇮🇹Milan, Italy
Investigator site 39 - IT0390006
🇮🇹Pisa, Italy
Investigator Site 32 - DE0490001
🇩🇪Essen, Germany
Investigator Site 31 - IT0390005
🇮🇹Bologna, Italy
Investigator Site 30 - IT0390004
🇮🇹Genova, Italy
Investigator Site 34 - DE0490005
🇩🇪Hannover, Germany
Investigator Site 5 - PL0480002
🇵🇱Kraków, Poland
Investigator Site 19 - ES0340001
🇪🇸Barcelona, Spain
Investigator Site 22 - IT0390001
🇮🇹Roma, Italy
Investigator Site 8 - US0010003
🇺🇸Chicago, Illinois, United States
Investigator Site 13 - US0010013
🇺🇸Portland, Oregon, United States
Investigator Site 24 - FR0330004
🇫🇷Lille, France
Investigator Site 23 - FR0330005
🇫🇷Bordeaux, France
Investigator site 37 - CA0019002
🇨🇦Québec, Canada
Investigator Site 1 - GEO9950001
🇬🇪Tbilisi, Georgia
Investigator Site 4 - PL0480001
🇵🇱Lubin, Poland
Investigator Site 18 - ES0340002
🇪🇸Santiago De Compostela, A Coruña, Spain
Investigator Site 15 - US0010014
🇺🇸Coral Springs, Florida, United States