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apadamtase alfa

Generic: Apadamtase Alfa

apadamtase alfa: 4 clinical trials tracked.

apadamtase alfa evidence translation

What we can confirm

4 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about apadamtase alfa, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence2 indications · 0 study sponsors

Study sponsors

No additional listed-company sponsor is linked.

Clinical Trial Registry Records (4)

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Safety, Tolerability, and Efficacy of TAK-755 in Acute Ischemic Stroke

NCT07392450Registry updated 2026-08-14·Phase 2
Recruiting

Primary endpoint: Part A and B: Percentage of Participants who Develop Symptomatic Intracranial Hemorrhage (sICH) as Defined by the Heidelberg Bleeding Classification System

InterventionalRandomizedquadruple222 targetStarted 2026-05Completion 2027-1250 sites · Belgium, Brazil, China, France…Takeda

A Phase 2b, Multicenter, Randomized, Double-blind Study of Safety and Efficacy of TAK-755 (rADAMTS13) With Minimal to No Plasma Exchange (PEX) in the Treatment of Immune-mediated Thrombotic Thrombocytopenic Purpura (iTTP)

NCT05714969Registry updated 2026-06-17·Phase 2
Completed

Primary endpoint: Incidence of Adverse Events (AEs), Serious Adverse Events (SAEs), and Adverse Event of Special Interest (AESIs) After Receiving any Dose of Investigational Product (IP)

InterventionalRandomizedquadruple29 enrolledStarted 2023-07Completion 2026-0422 sites · Austria, Greece, Italy, Spain…Takeda

A Phase 3b, Prospective, Open-label, Multicenter, Single Treatment Arm, Continuation Study of the Safety and Efficacy of TAK-755 (rADAMTS13, Also Known as BAX 930/SHP655) in the Prophylactic and On-demand Treatment of Subjects With Severe Congenital Thrombotic Thrombocytopenic Purpura (cTTP; Upshaw-Schulman Syndrome, or Hereditary Thrombotic Thrombocytopenic Purpura)

NCT04683003Registry updated 2026-04-02·Phase 3
Active, not recruiting

Primary endpoint: Incidence of Related Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)

Interventionalopen77 targetStarted 2021-04Completion 2027-0327 sites · Austria, China, France, Germany…Takeda

A Phase 3, Prospective, Randomized, Controlled, Open-label, Multicenter, 2 Period Crossover Study With a Single Arm Continuation Evaluating the Safety And Efficacy of BAX 930 (rADAMTS13) in the Prophylactic And On-demand Treatment of Subjects With Severe Congenital Thrombotic Thrombocytopenic Purpura (cTTP, Upshaw-Schulman Syndrome [USS], Hereditary Thrombotic Thrombocytopenic Purpura [hTTP])

NCT03393975Registry updated 2026-02-09·Phase 3
Completed

Primary endpoint: Number of Participants With Acute Thrombotic Thrombocytopenic Purpura (TTP) Events During Prophylactic Treatment

InterventionalRandomizedopen52 enrolledStarted 2017-10Completion 2024-0533 sites · Austria, France, Germany, Italy…Baxalta now part of Shire