c Ceftolozane-tazobactam is active against Gram-negative pathogens, including multidrug-resistant Pseudomonas aeruginosa. In a subgroup analysis of patients with complicated intra-abdominal infections (cIAIs) involving P. aeruginosa from a phase 3 program, ceftolozane-tazobactam demonstrated potent in vitro activity against P. aeruginosa. Clinical cure in the microbiologically evaluable population was 100% (26/26) for ceftolozane-tazobactam plus metronidazole and 93.1% (27/29) for meropenem. These findings support the use of ceftolozane-tazobactam in the management of cIAI when P. aeruginosa is suspected or confirmed. (This study has been registered at ClinicalTrials.gov under registration no. NCT01445665 and NCT01445678.) C omplicated intra-abdominal infections (cIAIs) are caused by Gram-negative bacteria, with Enterobacteriaceae being the most common pathogen. Pseudomonas aeruginosa is the thirdmost-common Gram-negative bacteria in cIAI (1), and increasing rates of P. aeruginosa resistance are a global concern (2, 3).Ceftolozane-tazobactam, in combination with metronidazole, is approved for the treatment of cIAI (4). Ceftolozane-tazobactam has potent activity against many drug-resistant Gram-negative pathogens, including most extended-spectrum -lactamase (ESBL)-producing Enterobacteriaceae (5, 6), and is minimally affected by common P. aeruginosa resistance mechanisms (7). Compared with approved -lactam antibiotics, including meropenem and piperacillin-tazobactam, ceftolozane-tazobactam displays more potent in vitro activity against P. aeruginosa (8).The Assessment of the Safety Profile and Efficacy of Ceftolozane/Tazobactam in Complicated Intra-Abdominal Infections (ASPECT-cIAI) study was a global phase 3 program that demonstrated the efficacy of ceftolozane-tazobactam plus metronidazole to be similar to that of meropenem in patients with cIAI (NCT01445665 and NCT01445678) (9). This analysis was conducted to determine the characteristics and clinical outcomes of the subgroup of patients with P. aeruginosa infection.( In ASPECT-cIAI, patients (age, Ն18 years) with cIAI were randomly assigned 1:1 to receive intravenous ceftolozane-tazobactam (1.5 g containing 1,000 mg ceftolozane and 500 mg tazobactam) plus metronidazole (500 mg) every 8 h or intravenous meropenem (1 g every 8 h) plus placebo for 4 to 14 days. Efficacy was assessed at the test-of-cure visit 24 to 32 days after initiation of the study drug. Clinical cure was defined as the resolution of or significant improvement in signs and symptoms of the index infection, such that no additional antibacterial therapy or intervention was necessary. Descriptive statistics were used to compare baseline characteristics (microbiological intent-to-treat [MITT] population) and clinical outcomes (microbiologically evaluable [ME] population) of patients with and without P. aeruginosa infection. Descriptions of inclusion/exclusion criteria and study design were published previously (9).MIC cutoffs for susceptibility to ceftolozane-tazobactam and meropenem were based ...