The objective of this pivotal Phase III study is to investigate the safety and efficacy of prulifloxacin versus placebo in the treatment of subjects with acute bacterial gastroenteritis.

This double-blind trial will compare the safety and efficacy of prulifloxacin versus placebo in adult travelers with acute gastroenteritis characterized by diarrhea with one or more of the following signs or symptoms: nausea, vomiting, abdominal pain or cramping, fecal urgency, moderate to severe gas-related symptoms, or tenesmus of ≤72 hours duration.

Inclusion Criteria:

• Diagnosis of Acute Bacterial Gastroenteritis;
• Traveler from Industrialized Country;
• Capable of giving Informed Consent

Exclusion Criteria:

• Fever (>100.3 degrees);
• Pregnant or Breast Feeding or Not using adequate birth control;
• Known or Suspected (co-)Infection with non-bacterial pathogen;
• Symptoms of Gastroenteritis of >72 hours;
• Bloody Diarrhea;
• Concomitant antibacterial with activity against enteric bacterial pathogens;
• History of IBD;
• Unable/Unwilling to comply with study protocol;
• > 2 doses of anti-diarrheal medication within 24 hours;
• Antimicrobial Treatment within 30 days