Skip to content

COMPARATIVE RANDOMIZED DOUBLE BLIND MULTICENTRIC STUDY WHICH EVALUATES THE EFFECTIVENESS, SAFETY AND TOLERABILITY OF MK-0826 VERSUS CEFEPIME IN THE TREATMENT OF HOSPITAL ACQUIRED PNEUMONIA IN ADULTS

COMPARATIVE RANDOMIZED DOUBLE BLIND MULTICENTRIC STUDY WHICH EVALUATES THE EFFECTIVENESS, SAFETY AND TOLERABILITY OF MK-0826 VERSUS CEFEPIME IN THE TREATMENT OF HOSPITAL ACQUIRED PNEUMONIA IN ADULTS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REPEC
Registry ID
PER-072-00
Enrollment
Unknown
Registered
2000-01-01
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Group 1 Type of group
MK-0826 once a day, plus 2 placebo doses of the antibiotic Cefepime every 12 hours. Group name:Group 2 Type of group
Cefepime every 12 hours, plus a placebo dose of the drug MK-0826.

Sponsors

MERCK SHARP & DOHME PERU S.R.L.,
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: N.A

Exclusion criteria

Exclusion criteria: • Patients under 18 years of age. • Patients who have received an effective antibiotic treatment for pneumonia for more than one day (24 hours). • Patients who have previously had serious allergies or other serious reactions to certain antibiotics, including Carbapenem, Cefepime or other penicillins or Cephalosporins or Metronidazole. • Patients who have a rapidly evolving disease or terminal illness. • Patients whose kidney or liver is working very poorly, determined by a blood test or those who require dialysis. • Patients who have AIDS or those who are taking medications that serve to lower the defenses (immunosuppressants). • Patients who are participating or have participated in another medical study that involves the use of a research drug, within the last 30 days or if you have participated in this study before. • Patients with lung cancer or cancer that has spread to the lung or cystic fibrosis.

Design outcomes

Primary

MeasureTime frame
Outcome name:NA Measure:NA Timepoints:NA

Secondary

MeasureTime frame
Outcome name:NA Measure:NA Timepoints:NA

Contacts

Public ContactStela Lopez

MERCK SHARP & DOHME PERU S.R.L

stela_lopez@merck.com4115935

Outcome results

None listed

Source: REPEC (via WHO ICTRP)