Table 1.
EU prescribing summary of RTS,S/AS01 malaria vaccine (Mosquirix®) [6]. Consult local prescribing information for further details
What is the approved indication? | |
Active immunisation of children aged 6 weeks up to 17 months against Plasmodium falciparum malaria and hepatitis B (article 58 approval) | |
Use should be based on official recommendations that consider the epidemiology of P. falciparum malaria in different geographical areas | |
How is RTS,S/AS01 available? | |
Powder (RTS,S antigen) and suspension (AS01 adjuvant), which must be reconstituted prior to administration | |
What is the composition of RTS,S/AS01? | |
After reconstitution, one 1 mL vial contains two 0.5 mL vaccine doses. One vaccine dose (0.5 mL) contains 25 µg of RTS,S, adjuvanted with AS01 | |
RTS,S is a portion of P. falciparum circumsporozoite protein fused with hepatitis B surface antigen (RTS) and combined with hepatitis B surface antigen (S) in the form of non-infectious virus-like particles produced in yeast (Saccharomyces cerevisiae) cells by recombinant DNA technology | |
AS01 is a liposome-based vaccine adjuvant that comprises 3-O-desacyl-4’- monophosphoryl lipid A (MPL) 25 µg and Quillaja saponaria Molina, fraction 21 (QS-21) 25 µg. MPL is manufactured by GSK while QA-21 is licensed by GSK from Antigenics LLC, a wholly owned subsidiary of Agenus Inc. | |
How should RTS,S/AS01 be stored? | |
Shelf-life is 3 years. Do not freeze the product. Store in the original package to protect it from light | |
From a microbiological standpoint, reconstituted RTS,S/AS01 should be used immediately, although chemical and physical in-use stability has been demonstrated for 6 h at 25° C. If not used immediately, normal storage time is < 6 h in a refrigerator (2°–8° C) | |
How should RTS,S/AS01 be administered? | |
Intramuscular injection; the preferred injection site in children aged ≥ 5 months is the deltoid muscle | |
What are the contraindications to the use of RTS,S/AS01? | |
Hypersensitivity to the active substance or any of the excipients of RTS,S/AS01, previous doses of RTS,S/AS01 or hepatitis B vaccines | |
What other special warnings/precautions pertain to the use of RTS,S/AS01? | |
Protection against P. falciparum malaria | Does not provide complete protection; may delay the natural acquisition of immunity; efficacy wanes over time; efficacy data limited to children from sub-Saharan Africa; does not protect against malaria caused by pathogens other than P. falciparum |
Protection against hepatitis B | Should not be used for the prevention of hepatitis B when prevention against P. falciparum malaria is not sought |
Infants at risk of bleeding | Administer with caution in individuals with thrombocytopenia or any coagulation disorders, as bleeding may occur after intramuscular injection |
Infants with immunodeficiency | No data other than for HIV infection for which data are limited |
Preterm infants (born ≤ 28 weeks of gestation) | When administering the first three doses, consider the potential risk of apnoea and the need for respiratory monitoring for 48–72 h in infants who remain hospitalized at the time of vaccination, particularly those with a history of respiratory immaturity |
Which vaccines can be administered concomitantly with RTS,S/AS01? | |
Monovalent or combination vaccines including diphtheria, tetanus, whole cell pertussis, acellular pertussis, hepatitis B, Haemophilus influenzae type b, oral polio, measles, rubella, yellow fever, rotavirus and pneumococcal conjugate vaccines | |
What are the potential clinically relevant drug interactions between RTS,S/AS01 and other drugs/vaccines? | |
Pneumococcal conjugate vaccines | May increase the risk of fever within 7 days after vaccination |
Rotavirus and pneumococcal conjugate vaccines | May reduce the antibody response to the circumsporozoite antigen of RTS,S/AS01 |
Immunosuppressive therapy | No data, but decreased efficacy cannot be ruled out |
Antipyretic prophylaxis | May decrease the immune response to the vaccine, and hence, not recommended |