Casimersen

CHEMBL4297566 Phase 4 Zugelassen Oligonucleotide
Half-Life
Bioavailability
Protein Binding
Molecular Weight
g/mol
LogP
Phase
4

An antisense oligonucleotide that targets a specific sequence in pre-messenger RNA to promote skipping of exon 45 of the dystrophin gene, allowing production of a truncated but partially functional dystrophin protein. It is approved for the treatment of Duchenne muscular dystrophy in patients with mutations amenable to this particular exon skipping. Treatment may slow disease progression in eligible patients.

Wirkmechanismus

Binds to complementary mRNA sequences through Watson-Crick base pairing, modulating gene expression by promoting mRNA degradation via RNase H or altering pre-mRNA splicing.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanismus

Binds to complementary mRNA sequences through Watson-Crick base pairing, modulating gene expression by promoting mRNA degradation via RNase H or altering pre-mRNA splicing.

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.

Häufig gestellte Fragen

An antisense oligonucleotide that targets a specific sequence in pre-messenger RNA to promote skipping of exon 45 of the dystrophin gene, allowing production of a truncated but partially functional dystrophin protein. It is approved for the treatment of Duchenne muscular dystrophy in patients with mutations amenable to this particular exon skipping. Treatment may slow disease progression in eligible patients.

Binds to complementary mRNA sequences through Watson-Crick base pairing, modulating gene expression by promoting mRNA degradation via RNase H or altering pre-mRNA splicing.

Yes, Casimersen is an approved drug. It has reached clinical phase 4. It is classified as a Oligonucleotide.

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References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL4297566. Open-access bioactivity database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-02-27.

Medizinischer Haftungsausschluss

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.

Data sources: ChEMBL, PubChem, DailyMed.