Haemophilus influenzae type B strain 20752 capsular polysaccharide tetanus toxoid conjugate antigen

Haemophilus influenzae type b strain 20752 capsular polysaccharide tetanus toxoid conjugate antigen is an active immunization as a booster dose given intramuscularly to pediatric patients who have received a primary... The vaccine contains Haemophilus b capsular polysaccharide (polyribosyl-ribitol-phosphate PRP), which is a high molecular weight polymer prepared from the Haemophilus influenzae type b strain 20,752.

Primary indication
Indicated for active immunization in pediatric patients 15 months through 4 years of age as a booster dose for the prevention of invasive disease caused by Haemophilus influenzae type b.Curator reviewed · 2 structured indications
First approval
Canada, 2001 · United States, 2009
Also known as
Haemophilus influenzae type b strain 20752, capsular polysaccharide inactivated tetanus toxoid conjugate vaccine · Haemophilus influenzae type B-PRP and tetanus toxoid conjugate (PRP-T)
Brand names
  • Hiberix

Resolves to

Clinical / RWD

What you can answer from here — as of April 02, 2025

290Drug interactionsStructured to mechanism, not free text
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22Clinical trialsPhase, status and sponsor resolved per trial
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2Structured indicationsCondition, population, route and combination as fields, not prose
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8Marketed productsAcross 5 countries and 3 labellers
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Which other approved drugs treat the same conditions as Haemophilus influenzae type B strain 20752 capsular polysaccharide tetanus toxoid conjugate antigen, and which companies have late-stage candidates in those indications?

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