Robust Late‑Stage Pipeline and Clinical Success
Delivered 3-for-3 positive Phase III readouts (oveporexton, rusfertide, zasocitinib) in FY2025; TAK-881 showed positive pivotal results (20% facilitated SCIG, comparable efficacy to HYQVIA at half the Ig volume). Oveporexton and rusfertide granted FDA priority review with potential U.S. launches in H2 2026; zasocitinib planned for commercialization in H1 2027. Management expects this late-stage depth to be the most robust in Takeda's history and to support an average of 2–3 NME filings or major U.S. indication expansions per year through 2030.