ADC Program | Target | Indication | Platform | Phase |
---|---|---|---|---|
upifitamab rilsodotin (UpRi)* |
NaPi2b | Platinum-Resistant Ovarian Cancer | Dolaflexin | P2 Pivotal Study |
upifitamab rilsodotin (UpRi)* |
NaPi2b | Recurrent Platinum-Sensitive Ovarian Cancer Maintenance | Dolaflexin | P3 |
upifitamab rilsodotin (UpRi)* |
NaPi2b | Platinum-Sensitive Ovarian Cancer | Dolaflexin | P1 Dose Expansion |
XMT-1660 | B7-H4 | Multiple Solid Tumors | Immunosynthen | P1 Dose Escalation |
XMT-2056** | Novel HER2 Epitope | Multiple Solid Tumors | Immunosynthen | P1 Dose Escalation |
XMT-2068 | Undisclosed | Undisclosed | Immunosynthen | Discovery |
XMT-2175 | Undisclosed | Undisclosed | Immunosynthen | Discovery |
Multiple Programs | Undisclosed | Undisclosed | Immunosynthen Dolasynthen Dolaflexin |
Preclinical |
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Multiple | Undisclosed | Immunosynthen | Discovery |
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Multiple | Undisclosed | Dolasynthen | Discovery |
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Multiple | Undisclosed | Dolaflexin | Preclinical |
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5T4 | Undisclosed | Dolaflexin | P1 Dose Escalation |
*NaPi2b antibody used in UpRi (formerly XMT-1536) is in-licensed from Recepta Biopharma. Recepta has rights to commercialize UpRi in Brazil.
**XMT-2056 is wholly owned by Mersana, with GSK having an exclusive global license option to co-develop and commercialize the candidate