Effectiveness and Safety of Zilucoplan Treatment for French Patients With Myasthenia Gravis Over 3 Months

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire de Nice

About this trial

This study called "Multicenter Retrospective Study on the Short- and Medium-Term Efficacy and Tolerance of Zilucoplan Therapy in a Cohort of French Patients with Anti-AChR Myasthenia Gravis", is investigating the effects of a new treatment called Zilucoplan (generic name: ZILBRYSQ) on patients in France with a condition known as myasthenia gravis. Myasthenia gravis is an autoimmune disease that causes muscle weakness that worsens throughout the day with activity and impacts the ability to work and perform daily activities. The study aims to see if Zilucoplan can improve muscle strength and quality of life over three months, while also assessing its tolerance and safety by monitoring side effects. Researchers hope this treatment will offer significant benefits for people with this challenging condition.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

The study population will be selected from all the public hospitals in France where patients with confirmed myasthenia gravis with anti-AChR antibodies are given Zilucoplan as treatment under restricted access

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • Zilbrysq

    Drug

    Zilbrysq is a medicine used to treat generalized myasthenia gravis anti-AChR (a disease that leads to muscle weakness and tiredness) in adults whose immune system produces antibodies against a protein called the acetylcholine receptor. It is given as a subcutaneous injection (under the skin) once daily in a prefilled syringe that can be self-injected, and the dose depends on the patient's body weight. There are 3 available doses: 16.6 mg/0.416 mL for patients weighing less than 56 kg (123 lbs); 23 mg/0.574 mL for patients between 56 kg and less than 77 kg (123-170 lbs); and 32.4 mg/0.81 mL for patients weighing 77 kg and above (\>170 lbs). This can be injected into the abdomen, front of the thighs, and back of the upper arms (only if administered by a caregiver),

Treatment groups

55 Participants
are divided into 1 treatment group
Group A: Patients with Anti-AChR Myasthenia Gravis treated with Zilucoplan1 intervention

Trial outcomes

Primary outcomes

1

MG-ADL scores

The MG-ADL is an 8-item patient-reported scale that measures myasthenia gravis symptoms and functional status. It assesses the impact of Myasthenia Gravis on the daily functions of the patients

Time frame
At the inclusion, at 1 month, at 3 months and at 6 months

Secondary outcomes

1

Garches scale scores

The Garches scale is a 9-item based on clinical examination which measures the severity of myasthenia symptoms and muscle function.

Time frame
At the inclusion, at 1 month, at 3 months and at 6 months
2

Evaluation of tolerance (M6) through the description of type of Adverse events

Collect data on adverse events: total number of events, classification by type (mild, moderate, severe based on the " Common Terminology Criteria for Adverse Events (CTCAE) " scale)

Time frame
At 6 months
3

Evaluation of tolerance (M6) through the description of the frequency of Adverse event

number of adverse event per month

Time frame
At 6 months
4

Adverse events possible association with the treatment (causality)

causality (Certain / probable / possible / Unlikely / conditional / Unassessable)

Time frame
At 6 months

Other outcomes

Sponsors and contacts

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