Uncomplicated gonorrhea of 122 mucosal sites in 51 women was successfully treated with either a single intramuscular dose of 250 mg of ceftriaxone (23 patients) or two intramuscular doses of 4.8 x 106 U of aqueous procaine penicillin G (28 patients). Women treated with ceftriaxone had 22 cervical, 12 urethral, 10 anal canal, and 5 pharyngeal infections. All 122 pretreatment isolates were inhibited by 0.0125 ,ug or less of ceftriaxone per ml. The minimal concentration needed to inhibit 90% of isolates was 0.006 ,ug/ml for ceftriaxone and 0.2 ,ug/ml for penicillin G. Ceftriaxone was very well tolerated and caused no toxicity.Ceftriaxone (Ro 13-9904) is a new third-generation cephalosporin with enhanced in vitro activity against most gram-negative aerobic bacteria (2-4, 12, 14), including Neisseria gonorrhoeae (2,5,8,9,12,14). All gonococcal strains tested, whether ,-lactamase positive (9, 12) or negative (2,5,8,9,12,14), were sensitive to 0.03 ,ug/ml or less. The pharmacokinetics of ceftriaxone make it favorable for treating gonorrhea (10, 11); a single intramuscular 0.5-g dose in 1% lidocaine (10) produces peak serum levels of 42 jig/ml, with an elimination half-life of 7.0 h, uniquely long among P-lactam antibiotics. The lidocaine diluent apparently does not alter either elimination parameters or bioavailability of ceftriaxone, whereas it considerably reduces intensity and frequency of pain at the injection site (10).In a dose-ranging study of single intramuscular injections of 125, 250, and 500 mg, 46 men with uncomplicated gonorrhea were successfully treated (5) Patients were selected by a computer-generated randomization schedule (Hoffmann-La Roche Inc., Nutley, N.J.) to receive either 250 mg of ceftriaxone (dissolved in 1.0 ml of 1% lidocaine) as a single intramuscular dose or 4.8 x 106 U of APPG as two intramuscular doses with 1 g of probenecid by mouth. All injections were given into gluteal muscles. To be evaluable, women must have had positive cultures for N. gonorrhoeae on the day of treatment and must have returned for a test-of-cure within 4 to 7 days. Treatment success was defined by negative cultures for N. gonorrhoeae at the test-of-cure visit. Adverse reactions to treatment were monitored by a questionnaire about symptoms and by pre-and posttreatment complete blood counts, quantitative platelet counts, hemoglobin, hematocrit, blood urea nitrogen, serum creatinine, serum glutamic oxalacetic transaminase, serum glutamic pyruvic transaminase, total bilirubin, and urinalyses.Two cotton-tipped swab specimens each were obtained from the endocervix, urethra, anal canal, and posterior pharynx of all women at pretreatment and test-of-cure visits, directly inoculated onto modified