Table 1.
Agent | Manufacturer | Type of antibody | Mode of action | State of development | Indication |
---|---|---|---|---|---|
SYSTEMIC APPLICATION ROUTE | |||||
Actoxumab | Merck Sharp & Dohme Ltd (Europe), Inc. | Antitoxin A (CDA1, MK-3415) human monoclonal IgG antibody | Prevents binding to a cognate receptor | Terminated after phase III trial | None |
Bezlotoxumab | Merck Sharp & Dohme Ltd (Europe), Inc. | Antitoxin B (CDB1, MDX-1388, MK-6072) human monoclonal IgG antibody | Prevents binding to a cognate receptor | FDA and EMA approved | rCDI |
IVIG | Various | Human IgG | Neutralization of TcdA/TcdB | Market (for other indications) | rCDI/CDI/severe CDI |
ORAL APPLICATION ROUTE | |||||
IgAbulin | ImmunoAG Vienna/Baxter |
Human IgA | Neutralization of TcdA/TcdB | Market (for other indications) | CDI |
Oral hyperimmune bovine immunoglobulin concentrate (BIC) | Beth Israel Deaconess Medical Center |
Polyclonal antibody-enriched colostral immune whey protein concentrate | Neutralization of TcdA/TcdB | Clinical phase I | CDI |
MucoMilk | MucoVax BV | Polyclonal antibody-enriched milk immune whey protein concentrate | Neutralization of TcdA/TcdB, Binding of vegetative bacterial cells | Clinical development | rCDI |
Cediff | Novatreat Ltd. | Polyclonal antibody-enriched colostral immune whey protein concentrate | Binding of toxigenic vegetative bacterial cells | Interrupted in clinical phase II | rCDI |
IMM-529 | Immuron Ltd. | Immune colostrum concentrate | Neutralization of TcdB, Binding of vegetative bacterial cells and endospores | Clinical phase I/II | CDI/rCDI |
IVIG, intravenous immunoglobulin; TcdA, C. difficile toxin A; TcdB, C. difficile toxin B; CDI, C. difficile disease; rCDI, recurrent CDI.