Berdazimer

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Berdazimer

1846565-00-1

CAS NA SALT, 1846565-00-1

FDA APPROVE 1 /5/2024, To treat molluscum contagiosum
Drug Trials Snapshot

  • NVN-1000 free acid
  • NVN1000 free acid
  • Silsesquioxanes, 3-(2-hydroxy-1-methyl-2-nitrosohydrazinyl)propyl 3-(methylamino)propyl, polymers with silicic acid (h4sio4) tetra-et ester, hydroxy-terminated

Berdazimer sodium, sold under the brand name Zelsuvmi, is a medication used for the treatment for molluscum contagiosum.[1] Berdazimer sodium is a nitric oxide releasing agent.[1] It is a polymer formed from sodium 1-hydroxy-3-methyl-3-(3-(trimethoxysilyl)propyl)-1-triazene-2-oxide and tetraethyl silicate.[2]

Berdazimer sodium was approved for medical use in the United States in January 2024.[3][4][5]

Medical uses

Berdazimer sodium is indicated for the topical treatment of molluscum contagiosum.[1]

Pharmacology

Mechanism of action

Berdazimer sodium is a nitric oxide releasing agent.[1] The mechanism of action for the treatment of molluscum contagiosum is unknown.[1]

Pharmacodynamics

The pharmacodynamics of berdazimer sodium are unknown.[1]

Society and culture

Legal status

Berdazimer sodium was approved for medical use in the United States in January 2024.[4]

Names

Berdazimer sodium is the international nonproprietary name.[6]

Berdazimer

Berdazimer is a polymeric substance consisting of a polysiloxane backbone (Si-O-Si bonds) with covalently bound N-diazeniumdiolate nitric oxide (NO) donors. It releases NO through exposure to proton donors like water, which will degrade the N-diazeniumdiolate entity.2 Berdazimer was previously investigated as a potential treatment for molluscum contagiosum, a viral cutaneous infection mainly affecting children, sexually active adults, and immunocompromised patients. It is one of the 5 most prevalent skin diseases in the world and the third-most common viral skin infection in children.3 Previously, the first line treatment for molluscum contagiosum was surgical excision, although it poses challenges such as repeated doctor visits, post-surgical scarring and skin discoloration, and fear and anxiety in the pediatric population.3

On Jan 05, 2024, the FDA approved berdazimer under the brand name ZELSUVMI for the treatment of adult and pediatric molluscum contagiosum, and it is the first drug to be approved for this condition. This decision is based on positive results demonstrated in 2 Phase 3 trials, B-SIMPLE 4 and B-SIMPLE 2, where reduced lesion counts were observed with once-a-day uses of berdazimer.5

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References

  1. Jump up to:a b c d e f g h i “Zelsuvmi (berdazimer) topical gel” (PDF)Archived (PDF) from the original on 19 January 2024. Retrieved 9 January 2024.
  2. ^ “GSRS”gsrs.ncats.nih.govArchived from the original on 8 January 2024. Retrieved 8 January 2024.
  3. ^ “Drug Approval Package: Zelsuvmi”U.S. Food and Drug Administration (FDA). 2 February 2024. Archived from the original on 11 March 2024. Retrieved 11 March 2024.
  4. Jump up to:a b “Novel Drug Approvals for 2024”U.S. Food and Drug Administration (FDA). 29 April 2024. Archived from the original on 30 April 2024. Retrieved 30 April 2024.
  5. ^ “U.S. Food and Drug Administration Approves Zelsuvmi as a First-in-Class Medication for the Treatment of Molluscum Contagiosum”. Ligand Pharmaceuticals. 5 January 2024. Archived from the original on 8 January 2024. Retrieved 8 January 2024 – via Business Wire.
  6. ^ World Health Organization (2018). “International nonproprietary names for pharmaceutical substances (INN): recommended INN: list 79”. WHO Drug Information32 (1). hdl:10665/330941.

Further reading

External links

Berdazimer sodium
Clinical data
Trade names Zelsuvmi
Other names SB206
License data
Routes of
administration
Topical
ATC code
  • None
Legal status
Legal status
Identifiers
CAS Number
DrugBank
UNII
KEGG
ChEMBL
Chemical and physical data
Formula Indeterminate[1]
Molar mass Indeterminate[1]

/////Berdazimer, Zelsuvmi, FDA 2024, APPROVALS 2024, NVN-1000 free acid, NVN1000 free acid

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