Delandistrogene Moxeparvovec
A gene therapy that delivers a shortened but functional version of the dystrophin gene to muscle cells in patients with Duchenne muscular dystrophy. It uses a viral vector to introduce genetic instructions that help muscles produce a protective protein.
กลไกการออกฤทธิ์
Delivers functional copies of a gene to target cells using a viral vector, restoring expression of the deficient protein and correcting the underlying genetic defect.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Delivers functional copies of a gene to target cells using a viral vector, restoring expression of the deficient protein and correcting the underlying genetic defect.
HBD / HBA
- / -
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
คำถามที่พบบ่อย
A gene therapy that delivers a shortened but functional version of the dystrophin gene to muscle cells in patients with Duchenne muscular dystrophy. It uses a viral vector to introduce genetic instructions that help muscles produce a protective protein.
Delivers functional copies of a gene to target cells using a viral vector, restoring expression of the deficient protein and correcting the underlying genetic defect.
Yes, Delandistrogene Moxeparvovec is an approved drug. It has reached clinical phase 4. It is classified as a Gene.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL4650241. Open-access bioactivity database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-02-27.
ข้อจำกัดความรับผิดชอบทางการแพทย์
This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.
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