Regeneron seeks to edge Roche out of DME space

Share this article:
Eylea outduels Lucentis for physician mindshare, survey shows
Eylea outduels Lucentis for physician mindshare, survey shows

A year after its eye drug Lucentis landed the FDA's approval for diabetic macular edema, Roche's hold on this Eylea-free zone of the market may soon be ending. Regeneron, Eylea's manufacturer, said Tuesday that it expects to submit an NDA for this very same indication to the FDA this year, while its European marketing partner, Bayer, is on track to do the same abroad.

This would mean more than a me-too in the diabetic macular edema (DME) space. As noted by Forbes, Lucentis has a downside in that its label has a fatality warning. Eylea's does not, and that could give the Regeneron drug an edge if it too gets approved for use in DME.

It's not the first threat to Lucentis' hold on the eye market. The wet macular-degeneration drug saw immediate competition from off-label use of Genentech's Avastin, then from macular-degeneration newcomer Eylea.

DME is linked to blurry vision and even blindness, and estimates say it affects about 560,000 Americans.
Share this article:

Email Newsletters

More in News

Lack of marketing partner delays Afrezza launch

Lack of marketing partner delays Afrezza launch

Afrezza was heralded as one of the most innovative diabetes products of the last decade. So, why hasn't MannKind set a firm launch date for the product?

In sunny world of LASIK marketers, a dark underbelly

In sunny world of LASIK marketers, a dark ...

Last week, the former FDA branch chief who originally approved LASIK machines asked FDA to reconsider its denial last month of his petition to ban these devices.

BMS Q2 sales slip, Eliquis, Yervoy soar

BMS Q2 sales slip, Eliquis, Yervoy soar

The company attributed part of the Eliquis boost to the BMS-Pfizer DTC and education efforts.