Overview
Meningococcal group W-135 polysaccharide is group-specific polysaccharide antigens extracted and purified from Neisseria meningitidis serogroup W-135. N. meningitidis is a bacteria that causes endemic and epidemic diseases including meningitis and meningococcemia. It is subcutaneously administered as an active immunization against the invasive meningococcal disease caused by the serogroup W-135.
Indication
No indication information available.
Associated Conditions
- Invasive Meningococcal Infection caused by Neisseria meningitidis serogroup W-135
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|
No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| No FDA approvals found for this drug. | |||||
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
|---|---|---|---|
| No EMA approvals found for this drug. | |||
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| Menactra®, solution for injection | SIN13922P | INJECTION, SOLUTION | 4 mcg/dose (0.5 ml) | 2/24/2011 | |
| Menveo Powder and Solution for Solution for Injection | SIN14083P | INJECTION, POWDER, FOR SOLUTION | 5 microgram conjugated to 3.3-8.3 microgram | 1/20/2012 | |
| MENQUADFI SOLUTION FOR INJECTION | SIN16454P | INJECTION, SOLUTION | 10 mcg / 0.5mL | 3/29/2022 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
|---|---|---|---|---|---|
| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
|---|---|---|---|---|---|
| No PPB approvals found for this drug. | |||||
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| MENVEO Meningococcal (Groups A,C,W-135 and Y) Oligosaccharide CRM197 solution for injection vial | 393321 | Medicine | A | 9/26/2023 | |
| NIMENRIX Meningococcal (Groups A, C, W-135, Y) Polysaccharide Tetanus Toxoid Conjugate Vaccine, injection vial and diluent syringe | 199742 | Medicine | A | 8/29/2013 | |
| MenQuadfi meningococcal (Groups A,C,Y,W) polysaccharide tetanus toxoid conjugate vaccine, solution for injection, vial | 325682 | Medicine | A | 10/29/2020 | |
| MENVEO meningococcal (Groups A, C, W-135 and Y) oligosaccharide CRM197 conjugate vaccine | 192696 | Medicine | A | 5/23/2012 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| MENOMUNE-A/C/Y/W-135 | aventis pasteur limited | 02161184 | Powder For Solution - Subcutaneous | 2.5 MG / KIT | 8/13/1998 |
| NIMENRIX | 02402904 | Powder For Solution
,
Kit - Intramuscular | 5 MCG / 0.5 ML | 8/22/2013 | |
| MENOMUNE-A/C/Y/W-135 | 00588490 | Powder For Solution - Subcutaneous | 500 MCG / KIT | 12/31/1983 | |
| MENOMUNE-A/C/Y/W-135 | 01959018 | Powder For Solution
,
Kit - Subcutaneous | 50 MCG / 0.5 ML | 10/29/1993 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| No CIMA AEMPS (Spain) approvals found for this drug. | |||||
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Malaysia NPRA approvals found for this drug. | |||||
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
|---|---|---|---|---|---|
| No UK EMC drug information found for this drug. | |||||
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