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Ropivacaine

Alternative Names: ropivacaine, naropin, naropeine, naropine, ropivacaïne, ropivocaine, Ropivicaine, prf-110, prf 110, prf110, tlc-590, tlc590, tlc 590, ropivacain
Latest Update: 2024-12-19
Latest Update Note: Clinical Trial Update

Product Description

Ropivacaine is a long-acting amide local anaesthetic agent and first produced as a pure enantiomer. It produces effects similar to other local anaesthetics via reversible inhibition of sodium ion influx in nerve fibres. Ropivacaine is less lipophilic than bupivacaine and is less likely to penetrate large myelinated motor fibres, resulting in a relatively reduced motor blockade.

Mechanisms of Action: CYP2D6 Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Approved

Approved Countries: Argentina | Australia | Austria | Bangladesh | Belgium | Brazil | Bulgaria | Canada | Chile | China | Colombia | Croatia | Cyprus | Czech | Denmark | Dominican Republic | Egypt | Estonia | Finland | France | Germany | Greece | Hong Kong | Hungary | India | Indonesia | Ireland | Israel | Italy | Korea | Latvia | Lebanon | Lithuania | Luxembourg | Malaysia | Malta | Mexico | Netherlands | New Zealand | Norway | Pakistan | Peru | Philippines | Poland | Portugal | Romania | Russia | Saudi Arabia | Singapore | Slovakia | Slovenia | South Africa | Spain | Sweden | Switzerland | Taiwan | Tunisia | Ukraine | United Arab Emirates | United Kingdom | United States | Uruguay | Venezuela | Vietnam

Approved Indications: None

Known Adverse Events: None

Company: Zhejiang University
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Ropivacaine

Countries in Clinic: Canada, China, Czech Republic, France, Germany, Italy, Mexico, Poland, United States, Unknown Location

Active Clinical Trial Count:

Highest Development Phases

Phase 3: Bunion|Osteoarthritis, Knee|Pain, Postoperative|Total Knee Arthroplasty

Phase 2: Anesthesia Related

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

TLC590A2006

P2

Recruiting

Pain, Postoperative

2026-07-01

TLC590A2003

P3

Not yet recruiting

Pain, Postoperative

2025-12-01

95%

jRCT2031220354

P3

Recruiting

Osteoarthritis, Knee

2024-07-31

PRF-110-103

P3

Completed

Bunion

2024-07-30

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