Streptococcus pneumoniae type 9V capsular polysaccharide diphtheria CRM197 protein conjugate antigen
- Generic Name
- Streptococcus pneumoniae type 9V capsular polysaccharide diphtheria CRM197 protein conjugate antigen
- Brand Names
- Prevnar 13, Prevnar 20, Vaxneuvance
- Drug Type
- Biotech
- Unique Ingredient Identifier
- 5Q768OY0GI
Overview
Streptococcus pneumoniae type 9V capsular polysaccharide diphtheria CRM197 protein conjugate antigen is a sterile vaccine that contains saccharides of the capsular antigens of Streptococcus pneumoniae serotype 9v individually conjugated to the CRM197 protein, a nontoxic variant of diphtheria toxin isolated from cultures of Corynebacterium diphtheriae strain C7 (β197). It is contained in the vaccine under the market name Prevnar that contains the saccharides for serotypes 4, 6B, 9V, 14, 18C, 19F, and 23F for intramuscular injection. The saccharides in the vaccine are prepared from purified polysaccharides that are chemically activated then conjugated to the protein carrier CRM197 to form the glycoconjugate.
Background
Streptococcus pneumoniae type 9V capsular polysaccharide diphtheria CRM197 protein conjugate antigen is a sterile vaccine that contains saccharides of the capsular antigens of Streptococcus pneumoniae serotype 9v individually conjugated to the CRM197 protein, a nontoxic variant of diphtheria toxin isolated from cultures of Corynebacterium diphtheriae strain C7 (β197). It is contained in the vaccine under the market name Prevnar that contains the saccharides for serotypes 4, 6B, 9V, 14, 18C, 19F, and 23F for intramuscular injection. The saccharides in the vaccine are prepared from purified polysaccharides that are chemically activated then conjugated to the protein carrier CRM197 to form the glycoconjugate.
Indication
No indication information available.
Associated Conditions
- Otitis Media caused by Streptococcus pneumoniae serotype 9V
- Invasive Infection caused by Streptococcus pneumoniae serotype 9V
Clinical Trials
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No clinical trials found
No clinical trials found for this drug
FDA Approved Products
Product Name | Manufacturer | Route | Strength | Approved | NDC Code |
|---|---|---|---|---|---|
Wyeth Pharmaceutical Division of Wyeth Holdings LLC | INTRAMUSCULAR | 2.2 ug in 0.5 mL | 2025/04/18 | 0005-2000 | |
INTRAMUSCULAR | 2.2 ug in 0.5 mL | 2017/08/29 | 50090-1944 |
EMA Approved Products
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No EMA products found
No EMA products found for this drug
HSA Approved Products
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No HSA products found
No HSA products found for this drug
NMPA Approved Products
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No NMPA products found
No NMPA products found for this drug
PPB Approved Products
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No PPB products found
No PPB products found for this drug
TGA Approved Products
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No TGA products found
No TGA products found for this drug