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Currently, an ongoing phase III, multicenter, randomized, sham-controlled, double-blind trial is evaluating AT-04s efficacy and safety for endometriosis-related pain (dysmenorrhea, dyspareunia, chronic pelvic pain), with the primary outcome being the change in Numeric Rating Scale score at 16 weeks (36)

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Monitoring Requirements: Regular check-ins with your Healthcare Provider may be required to evaluate treatment progress and adjust dosage or frequency as needed

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