TherapeuticsMD has submitted the New Drug Application (NDA) for TX-001HR, the company’s investigational bio-identical hormone therapy combination of estradiol and progesterone in a single, oral softgel for the treatment of moderate-to-severe vasomotor symptoms due to menopause, with the U.S. Food and Drug Administration (FDA).
The NDA submission is supported by the complete TX-001HR clinical program, including positive results of the recently completed phase 3 Replenish Trial. The Company expects to learn of the acceptance of the NDA upon receipt of the Filing Review Notification from the FDA, approximately 74 days after the NDA submission.