Overview

LYS228 PK, Clinical Response, Safety and Tolerability in Patients With Complicated Intra-abdominal Infection (cIAI)

Status:
Terminated
Trial end date:
2018-09-24
Target enrollment:
0
Participant gender:
All
Summary
The purpose of the study was to evaluate whether LYS228 can be developed for the treatment of complicated intra-abdominal infections. It was planned that LYS228 exposure across patients with varying renal function would be evaluated during the study to confirm that LYS228 concentrations are predicted to be adequate to treat the patient population. It was planned that the PK exposure of the initial 8 patients would be analyzed. PK analysis was not conducted as per protocol the first analysis required 8 patients.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Novartis Pharmaceuticals
Treatments:
Anti-Bacterial Agents
Criteria
Inclusion Criteria:

- Male and female patients 18 to 85 years of age with visual confirmation (presence of
pus within the abdominal cavity) of an intra-abdominal infection associated with
peritonitis including at least one inclusionary diagnosis during surgical
intervention.

Exclusion Criteria

- Any of the excluded diagnoses: abdominal wall abscess, small bowel obstruction,
traumatic bowel perforation undergoing surgery within 12 hours, perforation of
gastroduodenal ulcer with surgery within 24 hours, an intra-abdominal process that is
not likely caused by infection.

- Pre-operative treatment of any duration with non-study Drug systemic antibiotic
therapy for peritonitis or abscess is not allowed unless certain criteria are met.

- Concomitant bacterial infection at time of enrollment requiring non-Study Drug
antibiotics and that may interfere with the evaluation of clinical response to the
study antibiotic.

- Known non-abdominal source of infection, including endocarditis, osteomyelitis,
abscess, meningitis, or pneumonia diagnosed within 7 days prior to enrollment.

- Patient has an Acute Physiology and Chronic Health Evaluation II (APACHE II) score >
30 or is considered, in the judgement of the investigator, unlikely to survive 4 weeks
(e.g. rapidly progressive terminal illness, including septic shock).

- Patients that meet sepsis criteria as defined by the quick sequential sepsis-related
organ failure assessment (qSOFA).

- Women of child-bearing potential unless they are using highly effective methods of
contraception during dosing and for 7 days after stopping study treatment.