🇺🇸 FDA
Pipeline program

A Dose-Finding, Adaptive, Randomized, Double-Blinded, Placebo-Controlled Trial to Evaluate the Safety, Tolerability, and Efficacy of TAK-360 in Participants with Idiopathic Hypersomnia (IH)

TAK-360-2002

Phase 2 other active

Quick answer

A Dose-Finding, Adaptive, Randomized, Double-Blinded, Placebo-Controlled Trial to Evaluate the Safety, Tolerability, and Efficacy of TAK-360 in Participants with Idiopathic Hypersomnia (IH) for Idiopathic Hypersomnia (IH) is a Phase 2 program (other) at Takeda Pharmaceuticals International AG with 1 ClinicalTrials.gov record(s).

Program details

Company
Takeda Pharmaceuticals International AG
Indication
Idiopathic Hypersomnia (IH)
Phase
Phase 2
Modality
other
Status
active

Clinical trials