Fervent Pharmaceuticals to Begin Menopause Therapy Trial

Fervent Pharmaceuticals has submitted an Investigational New Drug (IND) application to the U.S. Food and Drug Administration (FDA) for FP-101, its proprietary lead drug candidate for treating menopause symptoms, especially hot flashes.

A Phase 2a clinical trial will now begin to assess the therapeutic potential of FP-101 in post-menopausal women. The trial will get under way in the first quarter of 2018 and will enroll 110 women at a dozen study sites in Illinois, North Carolina, South Carolina and Tennessee. The North Carolina sites are in Cary, Charlotte, Hickory, Raleigh, Rocky Mount, Salisbury, Wilmington and Winston-Salem.

"We believe FP-101 has the potential to bring relief to millions of women suffering from hot flashes, night sweats and insomnia associated with menopause," said George Royster, founder, president and chief executive officer of Fervent. "Achievement of this regulatory milestone and the beginning of our clinical trial represents an important advancement in the development of FP-101."

FP-101 is an orally dosed, non-hormonal, non-herbal, non-antidepressant formulation of a compound that has known mechanisms of action, is already FDA approved for another undisclosed indication and has a long history of safe use.

Most FDA-approved treatments of symptoms in post-menopausal women involve estrogen hormone replacement therapy, which carries an increased risk of heart disease, breast cancer, deep vein thrombosis, stroke and gall bladder disease.

Fervent has received assistance from the North Carolina Biotechnology Center and its Eastern Regional Office, headed by Mark Phillips, vice president of statewide operations and executive director of the office.

The company is working with the University of Iowa Pharmaceuticals on drug formulation and with IQVIA (formerly QuintilesIMS) of Durham and PMG Research of Winston-Salem for clinical trial design and execution.