Ozmosi | TAK-085 Drug Profile

Product Description

TAK-085 is an oral capsule medicine licensed to Takeda Pharmaceutical Company Ltd. TAK-085 contains omega-3 fatty acid ethyl (mainly, ethyl eicosapentaenoate (EPA-E) and ethyl docosahexaenoic acid (DHA-E)). (Sourced from: https://clinicaltrials.gov/ct2/show/NCT01350999)

Mechanisms of Action: Unknown

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Takeda
Company Location: TOKYO M0 103-8668
Company CEO:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 4: Hyperlipoproteinemias|Hyperlipidemia

Phase 3: Hypertriglyceridemia

Trial ID	Trial	Phase	Trial Status	Disease	Primary Completion Date	Latest Trial Update Date	Data Updated
JapicCTI-163322	JapicCTI-163322	N/A	Completed	Hyperlipidemia	2017-08-30
NCT01350999	TAK-085/OCT-001	P3	Completed	Hypertriglyceridemia	2011-01-01	2024-06-06	Primary Endpoints\|Treatments
NCT01350973	TAK-085/CCT-002	P3	Completed	Hypertriglyceridemia	2010-12-01	2024-06-06
JapicCTI-090936	JapicCTI-090936	P3	Completed	Hypertriglyceridemia	None
JapicCTI-090937	JapicCTI-090937	P3	Completed	Hypertriglyceridemia	None
NCT02824432	Oasis Flow	P4	Completed	Hyperlipoproteinemias\|Hyperlipidemia	2017-08-19	2024-06-06

Recent News Events

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TAK-085

Alternative Names: tak-085, tak085, tak 085 Clinical Status: Inactive Latest Update: 2019-05-06 Latest Update Note: Clinical Trial Update