Ozmosi | Oritavancin Drug Profile
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Oritavancin

Pronounced as: or-i-ta-VAN-sin

Alternative Names: oritavancin, kimyrsa, orbactiv
Clinical Status: Active
Latest Update: 2026-02-02
Latest Update Note: News Article

Product Description

Oritavancin is a lipoglycopeptide with bactericidal activity against gram-positive bacteria.  (Sourced from: https://www.nejm.org/doi/full/10.1056/nejmoa1310422)

Mechanisms of Action: Cell Wall Inhibitor

Novel Mechanism: No

Modality: Peptide/Protein

Route of Administration: Intravenous

FDA Designation: *

Approval Status: Approved

Approved Countries: Austria | Belgium | Croatia | Czech | Estonia | European Medicines Agency | Finland | Germany | Greece | Hungary | Iceland | Ireland | Italy | Jordan | Latvia | Lithuania | Poland | Portugal | Saudi Arabia | Slovakia | Spain | Sweden | Switzerland | United Kingdom | United States

Approved Indications: None

Known Adverse Events: None

Company: Melinta
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Oritavancin

Countries in Clinic: Bulgaria, Greece, Latvia, Lithuania, Poland, Portugal, Romania, Spain, United States

Active Clinical Trial Count: 3

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Other

Phase 1: Gram-Positive Bacterial Infections

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT02134301

TMC-ORI-11-01

P1

Completed

Gram-Positive Bacterial Infections

2025-11-04

50%

2025-12-13

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

NCT05599295

ML-ORI-201

P2

Completed

Other

2025-11-20

2%

2025-11-26

2024-516385-10-00

ML-ORI-201

P2

Not yet recruiting

Unknown

2025-06-30

2%

2025-05-02

Treatments