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Relebactam

Alternative Names: relebactam, mk-7655, recarbrio
Latest Update: 2024-12-17
Latest Update Note: Clinical Trial Update

Product Description

Relebactam is a beta-lactamase inhibitor with the ability to inhibit a broad spectrum of beta-lactamases such as class A and class C beta-lactamases, including carbapenemases.  (Sourced from: https://pubmed.ncbi.nlm.nih.gov/32060929/)

Mechanisms of Action: LACTB Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: Austria | Belgium | Croatia | Cyprus | Czech | Estonia | European Medicines Agency | Finland | France | Germany | Greece | Hungary | Iceland | Ireland | Italy | Japan | Latvia | Lithuania | Netherlands | Norway | Poland | Portugal | Romania | Saudi Arabia | Serbia | Slovakia | Slovenia | Spain | Sweden | Taiwan | United Arab Emirates | United Kingdom | United States

Approved Indications: Urinary Tract Infections | Nephritis | Pyelonephritis

Known Adverse Events: Hypertension | Phlebitis | Headache | Diarrhea

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

Clinical Description

Map of Global Clinical Trials for Relebactam

Countries in Clinic: United States

Active Clinical Trial Count: 4

Highest Development Phases

Phase 3: Pneumonia, Bacterial|Pneumonia, Ventilator-Associated

Phase 2: Acute Respiratory Distress Syndrome|Febrile Neutropenia

Phase 1: Sepsis

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

NCI-2021-01957

P2

Completed

Febrile Neutropenia|Acute Respiratory Distress Syndrome

2023-10-06

Open-label Active-control Pediatric Safety, Efficacy, PK Study of MK-7655A

P3

Active, not recruiting

Unknown

2023-06-26

NCT04493151

P1

Completed

Sepsis

2023-05-31

IMI/REL (MK-7655A) vs. PIP/TAZ for Treatment of Subjects with HABP/VABP

P3

Completed

Pneumonia, Bacterial|Pneumonia, Ventilator-Associated

2022-01-09

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