News

Video

ASRS 2023: Subgroup analyses of the Phase 1 DAVIO Trial of EYP-1901

Nancy Lurker, spoke with our team about the subgroup analyses of the Phase 1 DAVIO Trial of EYP-1901 at the 2023 ASRS annual meeting.

Nancy Lurker, spoke with our team about the subgroup analyses of the Phase 1 DAVIO Trial of EYP-1901 at the 2023 ASRS annual meeting.

Video Transcript

Editor's note - This transcript has been edited for clarity.

Nancy Lurker:

Hi, I'm Nancy Lurker, the Executive Vice-Chair of the Board of EyePoint Pharmaceuticals. Dr J. Duker, our CEO, sends his regards [as] he was not able to make the meeting. We're very excited about some of the data that we presented at OIS on Thursday, here, ahead of ASRS in Seattle. In that presentation, we presented, most importantly, an interim safety update of masked data of our DAVIO 2 for wet AMD, double masked study, with an EYELA control.

That's 160 patients fully enrolled, and we expect the top line data read out to be this December. The goal of that study is to be able to show equal BCBA, non inferior, to EYELA and, most importantly, be able to show time to first supplementation, as well as total treatment burden reduction. Our goal is to be able to get a majority of patients out to 6 months or beyond with a tyrosine kinase inhibitor in our proven Durasert drug-delivery technology. Now, what we presented isn't this interim masked safety update in this 160 patient trial. What we're happy to report is that there were no drug-related, serious adverse events.

There were 2, but not drug-related. 1 was in the fellow eye [and] was a retinal hemorrhage. The other was a retinal detachment after the second aflibercept injection, but before either EYP-1901 or sham was injected. So far, the data looked very clean. Secondarily, we also presented patient demographics comparing our Phase 1 DAVIO study, which was a safety study of 17 patients, versus the DAVIO 2 study. What we have to show is that the patient demographics. The patients in DAVIO 1, because that was an all-comers trial, were sicker.

They had higher CST, 299 [in DAVIO 1] versus 266 in DAVIO 2. Vision was slightly worse, 70, 66 in DAVIO 1 versus 74 in DAVIO 2. We actually expect that we're getting a more representation patient population in DAVIO 2, the typical patient broad-based that you normally see in your practices. We're excited about where we are. We're looking forward to our update and top line readout in December of this year.


Newsletter

Don’t miss out—get Ophthalmology Times updates on the latest clinical advancements and expert interviews, straight to your inbox.

Related Videos
Lisa Nijm, MD, says preoperative osmolarity testing can manage patient expectations and improve surgical results at the 2025 ASCRS annual meeting
At the 2025 ASCRS Annual Meeting, Weijie Violet Lin, MD, ABO, shares highlights from a 5-year review of cross-linking complications
Maanasa Indaram, MD, is the medical director of the pediatric ophthalmology and adult strabismus division at University of California San Francisco, and spoke about corneal crosslinking (CXL) at the 2025 ASCRS annual meeting
(Image credit: Ophthalmology Times) ASCRS 2025: Taylor Strange, DO, assesses early visual outcomes with femto-created arcuate incisions in premium IOL cases
(Image credit: Ophthalmology Times) ASCRS 2025: Neda Shamie, MD, shares her early clinical experience with the Unity VCS system
Patricia Buehler, MD, MPH, founder and CEO of Osheru, talks about the Ziplyft device for noninvasive blepharoplasty at the 2025 American Society of Cataract and Refractive Surgeons (ASCRS) annual meeting
(Image credit: Ophthalmology Times) ASCRS 2025: Bonnie An Henderson, MD, on leveraging artificial intelligence in cataract refractive surgery
(Image credit: Ophthalmology Times) ASCRS 2025: Gregory Moloney, FRANZO, FRCSC, on rotational stability
Sheng Lim, MD, FRCOphth, discusses the CONCEPT study, which compared standalone cataract surgery to cataract surgery with ECP, at the 2025 ASCRS Annual Meeting.
(Image credit: Ophthalmology Times) ASCRS 2025: Steven J. Dell, MD, reports 24-month outcomes for shape-changing IOL
© 2025 MJH Life Sciences

All rights reserved.