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. 2022 Jan 18;12:838082. doi: 10.3389/fimmu.2021.838082

Figure 2.

Figure 2

Timeline of conceptual and technical innovations contributing to the development of the multi-function nanobody landscape. The Camelidae “heavy-chain-only antibodies” were first reported by Hamers-Casterman et al. (7) in 1993 and the first bispecific antibody (Catumaxomab) was approved by EMA only in 2009 (56). In 2014, the first bispecific scFv (Blinatumomab) was approved by FDA (57) and the same agency approved, the first bivalent nanobody drug (Caplacizumab) for treatment of acquired thrombotic thrombocytopenic purpura (TTP) in 2019 (58).