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Review Article

Antibody-drug conjugates: a mini-review. The synopsis of two approved medicines

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Pages 1662-1666 | Received 22 Oct 2014, Accepted 10 Dec 2014, Published online: 27 Jan 2015

Figures & data

Figure 1. Schematic of trastuzumab-Maytansine (T-DM1) including the [N-maleimidomethyl]cyclohexane-1-carboxylate (MCC) linker. An average of 3.5 DM1 molecules are conjugated to the Fc region of trastuzumab (Adapted from Krop et al., 2012).

Figure 1. Schematic of trastuzumab-Maytansine (T-DM1) including the [N-maleimidomethyl]cyclohexane-1-carboxylate (MCC) linker. An average of 3.5 DM1 molecules are conjugated to the Fc region of trastuzumab (Adapted from Krop et al., 2012).

Figure 2. Composition of brentuximab vedotin (cAC10-vcMMAE, SGN-35). SGN-30 (cAC10, the parent naked antibody) is a chimeric anti-CD30 monoclonal antibody derived from the fusion of the variable heavy and light region of the murine anti-CD30 antibody AC10, with the constant gamma1-heavy and kappa-light region of the human immunoglobulin (Adapted from Wahl et al., Citation2002; Doronina et al., Citation2006).

Figure 2. Composition of brentuximab vedotin (cAC10-vcMMAE, SGN-35). SGN-30 (cAC10, the parent naked antibody) is a chimeric anti-CD30 monoclonal antibody derived from the fusion of the variable heavy and light region of the murine anti-CD30 antibody AC10, with the constant gamma1-heavy and kappa-light region of the human immunoglobulin (Adapted from Wahl et al., Citation2002; Doronina et al., Citation2006).

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