Drugs / TAK-881

Trials 6

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 13 trials · 1 met primary
Phase 1 NCT06935266 Apr → Sep 2025 — Takeda Completed No outcome recorded
Phase 1 NCT06895967 Mar → Jul 2025 — Takeda Completed No outcome recorded
Phase 1 NCT05059977 Oct 2021 → Apr 2022 — Takeda Completed Met primary
Phase 2/31 trial · 1 met primary
Phase 2/3 NCT05755035 Oct 2023 → Jan 2026 immunodeficiency disease Takeda Completed Met primary
Phase 32 trials
Phase 3 NCT06747351 May 2025 → Jun 2028 expected chronic inflammatory demyelinating polyradiculoneuropathy Takeda Recruiting No outcome recorded
Phase 3 NCT06076642 Nov 2024 → May 2028 expected immunodeficiency disease Takeda Active not recruiting No outcome recorded
Comparator or background therapy1 trial
— NCT06955793 Background — immunodeficiency disease Takeda Available No outcome recorded

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 7 sources stand behind the page.

FieldValueCited text
Known as TAK-881 ClinicalTrials.gov intervention name — accepted as the source's own label NCT05059977 ↗
6

NCT06935266 ↗

NCT06747351 ↗

NCT06076642 ↗

NCT06955793 ↗

NCT05755035 ↗

NCT06895967 ↗

Modality Protein / enzyme biologic “Immune Globulin Subcutaneous (Human), 20% Solution with Recombinant Human Hyaluronidase (rHuPH20).” NCT05755035 ↗
Route Subcutaneous “Participants will receive subcutaneous infusion of TAK-881 on Day 1.” NCT05059977 ↗