A Clinical Trial to Assess the Safety and PK of OMN6 in HABP or VABP Caused by Acinetobacter Baumannii Complex

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-99
SponsorOmnix Medical Ltd

About this trial

This is a phase 2a, multinational, multicenter, double-blind, randomized, placebo-controlled, dose-ranging safety, tolerability and PK study in patients with HABP (Hospital Acquired Bacterial Pneumonia) or VABP (Ventilator Associated Bacterial Pneumonia) caused by ABC to identify safe and well-tolerated doses and to assess the PK profile of OMN6 in patients.

Eligibility criteria

Qualifiers

A signed informed consent form.

Male or female patients 18 years or older

A diagnosis of either a HABP or a VABP

ABC infection of the lower respiratory tract suspected based on a positive rapid testing of respiratory specimens

Disqualifiers

Moderate to severe reduction of renal function

Liver dysfunction

Evidence of septic shock

Acute respiratory distress syndrome.

Trial design

Treatments tested in this trial

  • OMN6
  • Placebo

Treatment groups

54 Participants
are divided into 2 treatment groups

Sponsors and collaborators