Ozmosi | Fosaprepitant Drug Profile
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Fosaprepitant

Alternative Names: fosaprepitant, mk-0517, mk0517, mk 0517, FOSAPREPITANT DIMEGLUMINE, FOCINVEZ
Clinical Status: Inactive
Latest Update: 2025-11-18
Latest Update Note: Clinical Trial Update

Product Description

a neurokinin-1 receptor antagonist for the prevention of chemotherapy-induced nausea and vomiting (Sourced from: https://pubmed.ncbi.nlm.nih.gov/18983233/)

Mechanisms of Action: NK1 Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Intravenous

FDA Designation: *

Approval Status: Approved

Approved Countries: Argentina | Australia | Austria | Belgium | Brazil | Canada | China | Colombia | Croatia | Dominican Republic | Egypt | Estonia | Germany | Hong Kong | Hungary | India | Italy | Japan | Malaysia | Mexico | Netherlands | New Zealand | Norway | Philippines | Russia | South Africa | Spain | Taiwan | Thailand | Turkey | United Arab Emirates | United Kingdom | United States | Venezuela

Approved Indications: None

Known Adverse Events: None

Company: Merck
Company Location: KENILWORTH NJ 07033
Company CEO: Robert M. Davis
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Oncology Unspecified

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

2018-000663-80

2018-000663-80

P3

Active, not recruiting

Oncology Unspecified

2019-05-11

2025-06-29

Primary Completion Date|Start Date|Study Completion Date|Treatments|Trial Status