MedPath
EMA Approval

Vaxchora

J07AE02

cholera, live attenuated

Vaccines

cholera vaccine, oral, live

Cholera

vibrio cholerae, strain cvd 103-hgr, live

Basic Information

EMA regulatory identification and product classification information

EMA Identifiers

ATC CodeJ07AE02
EMA European Classification

Overview Summary

Comprehensive product overview and regulatory summary

Vaxchora is a vaccine to prevent cholera disease in adults and children aged from 2 years. Cholera is a disease that is caught from contaminated food or drink and causes severe diarrhoea.

The vaccine contains a weakened form of the cholera bacterium Vibrio cholerae (serogroup O1).

Authorisations (1)

EMEA/H/C/003876

Bavarian Nordic A/S,Bavarian Nordic A/S,Philip Heymans Alle 3,11,DK-2900 Hellerup,Denmark

Authorised

April 1, 2020

Active Substances (1)

vibrio cholerae, strain cvd 103-hgr, live

Documents (11)

Vaxchora : EPAR - Public assessment report

April 8, 2020

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

CHMP summary of positive opinion for Vaxchora

January 31, 2020

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

Vaxchora : EPAR - Public assessment report

April 8, 2020

CHANGES_SINCE_INITIAL_AUTHORISATION

CHMP summary of positive opinion for Vaxchora

January 31, 2020

CHANGES_SINCE_INITIAL_AUTHORISATION

Vaxchora : EPAR - All authorised presentations

April 8, 2020

AUTHORISED_PRESENTATIONS

Vaxchora-H-C-003876-II-0003-G : EPAR - Assessment report - Variation

April 7, 2021

CHANGES_SINCE_INITIAL_AUTHORISATION

Vaxchora : EPAR - Procedural steps taken and scientific information after authorisation

June 22, 2020

CHANGES_SINCE_INITIAL_AUTHORISATION

CHMP post-authorisation summary of positive opinion for Vaxchora (II-03-G)

February 1, 2021

CHANGES_SINCE_INITIAL_AUTHORISATION

Vaxchora : EPAR - Product information

April 8, 2020

DRUG_PRODUCT_INFORMATION

Vaxchora : EPAR - Risk-management-plan summary

April 8, 2020

RISK_MANAGEMENT_PLAN_SUMMARY

Vaxchora : EPAR - Medicine overview

April 8, 2020

OVERVIEW_DOCUMENT

Overview Q&A (7)

Question

How is Vaxchora used?

Answer

Vaxchora can only be obtained with a prescription. It should be used according to official recommendations.

The vaccine is made up in water and taken by mouth as a single dose at least 10 days before the person is likely to come into contact with cholera bacteria.

For more information about using Vaxchora, see the package leaflet or contact your doctor or pharmacist.

Question

How does Vaxchora work?

Answer

When a person receives Vaxchora, the immune system (the body’s defences) recognises the weakened bacteria in the vaccine as foreign and makes antibodies against them. When the person comes into contact with potentially disease-causing cholera bacteria, the immune system will be ready to produce antibodies and in this way remove the bacteria quickly and so prevent cholera disease.

Question

What benefits of Vaxchora have been shown in studies?

Answer

A main study involving 197 healthy adults aged 18 to 45 years found that Vaxchora can prevent symptoms of cholera in people coming into contact with cholera bacteria.

In this study, individuals received a single dose of either Vaxchora or placebo (a dummy vaccine) and were then given infectious cholera bacteria (O1 strain). Moderate to severe diarrhoea (a symptom of cholera) occurred in about 6% of those given the cholera bacteria 10 days after Vaxchora and 12% of those given the bacteria 3 months after receiving Vaxchora. By comparison, moderate to severe diarrhoea occurred in 59% of adults who had received placebo.

Another main study involving 3,022 healthy adults aged 18 to 45 years found that antibodies against cholera bacteria were present after 11 days in 94% of adults who had received Vaxchora compared with 4% in those who received placebo.

Further studies confirmed that giving Vaxchora to adults aged 46 to 64 years or to children and adolescents aged 2 to 18 years was effective at producing antibodies against cholera bacteria.

Question

What are the risks associated with Vaxchora?

Answer

The most common side effects with Vaxchora (which may affect more than 1 in 10 people) are tiredness, headache, abdominal (belly) pain, feeling sick, vomiting and loss of appetite.

People who were born with problems with their immune system or are receiving treatment that weakens the immune system must not take Vaxchora.

For the full list of restrictions and side effects of Vaxchora, see the package leaflet.

Question

Why is Vaxchora authorised in the EU?

Answer

Vaxchora is effective for protecting vaccinated individuals against moderate and severe cholera disease. Measurement of antibodies after vaccination showed that it is effective in individuals from 2 years of age. The European Medicines Agency noted that evidence from Vaxchora studies is relevant only for travellers visiting areas where cholera is present. It is not known how long the protection lasts. The Agency considered that Vaxchora’s side effects are manageable. The Agency therefore decided that Vaxchora’s benefits are greater than its risks and it can be authorised for use in the EU.

Question

What measures are being taken to ensure the safe and effective use of Vaxchora?

Answer

The company that markets Vaxchora will provide a guide for healthcare professionals and a patient guide on how to make up and take the vaccine to avoid medication errors, especially in children aged 2 to 6 years.

Recommendations and precautions to be followed by healthcare professionals and those taking the vaccine for the safe and effective use of Vaxchora have also been included in the summary of product characteristics and the package leaflet.

As for all medicines, data on the use of Vaxchora are continuously monitored. Side effects reported with Vaxchora are carefully evaluated and any necessary action taken to protect those taking the vaccine.

Question

Other information about Vaxchora

Answer

Vaxchora received a marketing authorisation valid throughout the EU on 1 April 2020.

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