New drug hope for kids with rare Muscle-Weakening disease
NCT ID NCT06149559
First seen Jun 27, 2026 · Last updated Aug 14, 2026 · Updated 5 times
Summary
This study tests a drug called rozanolixizumab in 12 children aged 2 to 18 with moderate to severe generalized myasthenia gravis, a condition that causes muscle weakness. The goal is to see if the drug is safe and helps control symptoms. Participants receive injections, and researchers monitor side effects and changes in antibody levels.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- rozanolixizumab
- What this could lead to
- If it works, this could provide a new treatment option for children with generalized myasthenia gravis, helping control muscle weakness and improve daily life.
- What could go wrong
- This is a small, early-phase study with only 12 participants, so results may not apply to all children. The drug may cause serious side effects like infections or headaches.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Mg0006 20339
Ōbu, Japan
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Mg0006 20340
Fuchu-shi, Japan
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Mg0006 20343
Sagamihara, Japan
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Mg0006 40144
Milan, Italy
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Mg0006 40155
Warsaw, Poland
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Mg0006 40290
Bologna, Italy
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Mg0006 40733
Naples, Italy
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Mg0006 40734
Lodz, Poland
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Mg0006 40841
Yenimahalle, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Engineered immune cells take aim at debilitating muscle weakness
- New hope for myasthenia gravis: experimental drug CNP-106 enters human trials
- New hope for myasthenia gravis patients: experimental drug enters phase 2 trial
- New drug trial aims to ease muscle weakness in rare disease
- New shot could ease daily struggles for myasthenia gravis patients
- New study lets myasthenia gravis patients rate their own symptoms on a new drug