Glenmark Pharmaceuticals and the US-based Evestra Inc have completed a strategic development, license and commercialisation agreement to develop and market a generic version of Merck & Co’s NuvaRing product - etonogestrel/ethinyl estradiol vaginal ring – designed for women as an effective birth control option.
Development on the vaginal ring product is currently under way and the two companies expect to file an Abbreviated New Drug Application (ANDA) in fiscal 2019.
Evestra will develop this product exclusively for Glenmark for the US market, and will receive certain milestone payments during various stages of the product’s development, including royalties on net sales.
“Bringing high-quality and affordable options to market has been a core commitment for Glenmark since the beginning. The partnership with Evestra underscores that focus, and expands our portfolio into a leading non-daily contraceptive option prescribed to millions of women in the US,” said Robert Matsuk, president - North America and global API, Glenmark Pharmaceuticals Ltd.
Glenmark has secured exclusive marketing and distribution rights for the product, including an option to commercialise two additional Evestra vaginal ring products, for the US market.
Ze’ev Shaked, president and CEO, Evestra, added, “This is an important US-based strategic partnership for Evestra. By aligning our efforts, we expect to make great strides in improving women’s healthcare and access to options that are significantly more accessible due to their lower costs. We are excited to work with Glenmark.”
NuvaRing (etonogestrel/ethinyl estradiol vaginal ring) is an estrogen/progestin combination hormonal contraceptive (CHC) indicated for use by women to prevent pregnancy. According to IMS Health, Merck’s NuvaRing registered sales of $ 768 million in 2016 in the US market.
Evestra Inc is an emerging San Antonio-based biopharmaceutical research and development company with a therapeutic focus in women’s healthcare.
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