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John Hattie s Synthesis Of Approximately 800 Video

Data from a multicenter retrospective study of real-world usage of DEXYCU which demonstrated significant inflammatory reduction post-cataract surgery.

New data from an investigator-initiated open-label study comparing a drug treatment regimen of DEXYCU with Prolensa to a full post-operative eye drop treatment regimen which showed superior effects on inflammation, pain, visual acuity and patient preference in favor of the DEXYCU arm.

Importantly, patient out of pocket costs were 3. Jaffe, M. Data presented at AAO continues to show consistent efficacy and durability of YUTIQ in the treatment of chronic non-infectious uveitis affecting the posterior segment of the eye. Results from the second double-masked, randomized Phase e trial of YUTIQ were presented from patients with chronic non-infectious uveitis affecting the posterior segment of the eye, with eyes treated with YUTIQ and 52 eyes receiving sham injections.

At 36 months, the recurrence rate in YUTIQ-treated eyes was significantly lower than in sham-treated eyes Visual acuity gains or losses of 3 lines 080 more were both similar between treatment groups. Macular edema was resolved in Mean intraocular pressure IOP at 36 months was Intraocular pressure-lowering drops were used in Hovanesian, M.

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Data from an investigator-initiated study showed patients continue reading preferred a regimen of drug delivery of DEXYCU and Prolensa, a commonly used non-steroidal anti-inflammatory, compared to a full post-operative eye drop regimen. Pain was significantly reduced in the DEXYCU and Prolensa treatment group compared to a full post-operative eye John Hattie s Synthesis Of Approximately 800 treatment regimen. Ocular inflammation scores were significantly higher for the full post-operative eye drop treatment regimen compared to the DEXYCU and Prolensa regimen. Data also showed out of pocket costs were 3. Results presented from the post-approval, open-label, randomized, prospective, contralateral Oc study consisted of 30 patients 60 eyes undergoing routine cataract surgery.

Patients were randomized to receive DEXYCU intracameral, Moxifloxacin Intracameral, Prolensa or control Prednisolone drops, Moxifloxacin drops and Prolensa in the first eye and the alternative regimen in the second eye.

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No significant difference was noted in intraocular pressure IOP at any timepoint. Weinstock, M. Results from the real-world multicenter retrospective study demonstrated the anti-inflammatory efficacy and tolerability of DEXYCU that mirror the results seen in the controlled Phase 3 clinical trials. Mean intraocular pressure at postoperative day 1 was Each time point of data in the real-world study reflects patient chart data and frequency of measurement by participating physicians.

Real-world data of DEXYCU showed strong anti-inflammatory efficacy with and without additional topical anti-inflammatory treatment. Data at each timepoint in this real-world study reflects patient chart data and frequency of measurement by participating physicians. To learn more about the Company, please visit www.

All statements that address activities, events or developments that we intend, expect, plan or believe may occur in the future, including but not limited to statements about our expectations regarding the extent to which our business could be adversely impacted by the effects of the COVID coronavirus pandemic, as well as the timing and clinical development of our product candidates, including EYP; and the potential for EYP as a vital, novel six-month treatment for wet age-related macular degeneration.

Some of the factors that could cause actual results to differ materially from the anticipated results or other expectations expressed, anticipated or implied in our forward-looking statements are risks and uncertainties inherent in our business including, without limitation: the John Hattie s Synthesis Of Approximately 800 to which COVID impacts our business; the effectiveness and timeliness of clinical trials, and the usefulness of the data; the timeliness of regulatory approvals; our ability to achieve profitable operations and access to needed capital; fluctuations in our operating results; our ability to successfully produce Hatite commercial quantities of YUTIQ and DEXYCU and to successfully commercialize YUTIQ and DEXYCU in the U.

We cannot guarantee that the results and other expectations expressed, Approxiimately or implied in any forward-looking statement will be realized. A variety of factors, including these risks, could cause our actual results and other expectations to differ materially from the anticipated results or other expectations expressed, anticipated or implied in our forward-looking statements.

Should known or unknown risks materialize, or should underlying assumptions prove inaccurate, actual results could differ materially from past results and those anticipated, estimated or projected in Syntbesis forward-looking statements. Approximatey should bear this in mind as you consider any forward-looking statements. Our forward-looking John Hattie s Synthesis Of Approximately 800 speak only as of the dates on which they Apart Buildings Needs Society Architects Of Are made. We do not undertake any obligation to publicly update or revise our forward-looking statements even if experience or future changes makes it clear that any projected results expressed or implied in such statements will not be realized. Media: Thomas Gibson tom tomgibsoncommunications.

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