Various statements made in this presentation are forward-looking, and are inherently subject to risks, uncertainties and potentially inaccurate assumptions. All statements that address activities, events or developments

1 | EYEPOINT PHARMACEUTICALS Delivering Innovation to the Eye Investor Presentation August 2021 Exhibit 99.1

Various statements made in this presentation are forward-looking, and are inherently subject to risks, uncertainties and potentially inaccurate assumptions. 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 potential benefits of our partnerships and strategic alliances with other companies, as well as the timing and clinical development of our product candidates, including EYP-1901; the potential for EYP-1901 as a vital, novel twice-yearly treatment for wet age-related macular degeneration, diabetic retinopathy and retinal vein occlusion; and our longer term financial and business goals, are forward-looking statements. 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 effectiveness and timeliness of clinical trials, and the usefulness of the data; the timeliness of regulatory approvals; the extent to which COVID-19 impacts our business; our ability to achieve profitable operations and access to needed capital; fluctuations in our operating results; our ability to successfully produce sufficient commercial quantities of YUTIQ and DEXYCU and to successfully commercialize YUTIQ and DEXYCU in the U.S.; our ability to sustain and enhance an effective commercial infrastructure and enter into and maintain commercial agreements for YUTIQ and DEXYCU; the development of our YUTIQ line extension shorter-duration treatment for non-infectious uveitis affecting the posterior segment of the eye; the success of current and future license agreements, including our agreements with Ocumension Therapeutics and Equinox Science; termination or breach of current license agreements, including our agreements with Ocumension Therapeutics and Equinox Science; our dependence on contract research organizations, co-promotion partners, and other outside vendors and service providers; effects of competition and other developments affecting sales of products; market acceptance of products; effects of guidelines, recommendations and studies; protection of intellectual property and avoiding intellectual property infringement; retention of key personnel; product liability; industry consolidation; compliance with environmental laws; manufacturing risks; risks and costs of international business operations; volatility of our stock price; possible dilution; absence of dividends; and other factors described in our filings with the Securities and Exchange Commission. We cannot guarantee that the results and other expectations expressed, anticipated 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 the forward-looking statements. You should bear this in mind as you consider any forward-looking statements. Our forward-looking statements speak only as of the dates on which they 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. Forward Looking Statements

Proven technology driving pipeline growth 3 | EYEPOINT PHARMACEUTICALS Compelling pipeline focused on retinal disease

EYP-1901 - potential twice yearly anti-VEGF (TKI) treatment in Phase 1 wet AMD trial

YUTIQ50 - potential twice yearly treatment for posterior uveitis

Evaluating additional molecules using Durasert for potential pipeline addition

Durasert - FDA validated drug delivery platform

Sustained (zero-order kinetics) local delivery of drug product

Provides constant and stable release of therapeutics in the eye over weeks, months or years

Administered safely to thousands of patients' eyes across four FDA approved products including YUTIQ

Commercializing two FDA-approved products - YUTIQ and DEXYCU

Solid Q2 net product revenues as COVID-19 restrictions eased across the US during 1H 2021

5 | EYEPOINT PHARMACEUTICALS DURASERT Platform Proven sustained release intraocular drug delivery TECHNOLOGY 4 | EYEPOINT PHARMACEUTICALS

Proven sustained release delivery Four FDA-approved products with multiple programs in development Single in-office intravitreal injection

Continuous, stable release to the back of the eye provides consistent and reliable drug delivery over weeks, months or years

Simple administration in physician's office Approved Products

YUTIQ (2018, EyePoint) - Posterior Segment Uveitis

ILUVIEN (2014, Alimera) - DME

RETISERT (2005, B&L) - Uveitis

VITRASERT (1996, B&L) - CMV retinitis Development Candidates

EYP-1901 for Wet AMD

YUTIQ 50 for Posterior Segment Uveitis

Undisclosed preclinical programs 5 | EYEPOINT PHARMACEUTICALS

Building on a Proven Platform 6 | EYEPOINT PHARMACEUTICALS

17 | EYEPOINT PHARMACEUTICALS Retinal disease focused pipeline

EYP-1901 - Potential Twice a

Year Anti-VEGF Treatment 8 | EYEPOINT PHARMACEUTICALS PIPELINE Our goal is nothing short of transforming the treatment of wet AMD, diabetic retinopathy, and retinal vein occlusion

EYP-1901 Opportunity to transform the treatment of wet AMD The need...

Currently, wet AMD patients often lose vision despite anti-VEGF therapy due to undertreatment

The EYP-1901 solution...

Potential twice yearly in-office injection of anti-VEGF therapy

Anti-VEGF therapy (vorolanib) delivered via intravitreal injection using bioerodible Durasert

Sustained, stable release may lead to better visual outcomes through steady receptor blocking 9 | EYEPOINT PHARMACEUTICALS VEGF-vascular endothelial growth factor

Real world need... today's wet AMD treatments still result in vision loss over time PIPELINE

EYP-1901 Adjusted Mean Change From Baseline in VA Letter Score 3 6 12 Month 12 p=0.67 Aflibercept Ranibizumab 1.52 1.01 -0.19 1.24 0.71 -0.30 Follow-up (Month)

Lotery et al., Eye (2017) 31, 1697-1706 RETROSPECTIVE STUDY OF 3350 RANIBIZUMAB AND 4300 AFLIBERCEPT TREATMENT-NAIVE EYES WITH WET AMD 4

-4 0 10 | EYEPOINT PHARMACEUTICALS

Intravitreal delivery of vorolanib using a bioerodible formulation of Durasert

Tyrosine kinase inhibitor (TKI) studied as an oral therapy for wet AMD through Phase 2 with strong clinical signal and no significant ocular adverse events

Blocks all 3 isoforms of VEGFR, the main driver of the proliferation of blood vessels that are the hallmark of wet AMD PIPELINE EYP-1901 The EYP-1901 solution 11 | EYEPOINT PHARMACEUTICALS VEGFR- vascular endothelial growth factor receptor

23 | EYEPOINT PHARMACEUTICALS Effective blocking of VEGFR prevents neovascularization and loss of vision PIPELINE

EYP-1901 VEGF-B VEGF-C VEGF-D VEGF-A R1 / INFLAMMATION R2 / BLOOD VESSEL LEAKAGE R3 / BLOOD VESSEL GROWTH & LEAKAGE VEGF SIGNALING PATHWAYS VOROLANIB VOROLANIB VOROLANIB 12 | EYEPOINT PHARMACEUTICALS

A potent inhibitor of VEGFR

Vorolanib blocks VEGFR2 at the same level as sunitinib, a proven anti-VEGF therapy The inhibitor constant (Ki) of sunitinib for VEGFR is reported to be low (5 ng/mL), an indication of strong inhibition. Since Ki is related to IC50, similar inhibition Ki is expected for vorolanib. PIPELINE

EYP-1901 13 | EYEPOINT PHARMACEUTICALS IC50 - half maximal inhibitory concentration

Head-to-head study completed by Tyrogenix

Oral vorolanib clinical results - Phase 1

Demonstrated clinical activity in wet AMD Phase 1 trial design

Open label, 24 weeks, dose escalation, no control, oral delivery; 80% of eyes enrolled previously treated; 4 eyes treatment na ve

BCVA was maintained to within 4 letters of baseline at the 24-week endpoint, or improved in all but 1 participant

60% (15/25) of patients required no rescue injection while on oral vorolanib therapy

Excluding the 50 mg low dose, 72% of completers required no Anti-VEGF injection through the duration of the study (6 months)

Mean OCT thickness in completers was reduced by -50 +/- 97 m; Mean OCT thickness in treatment-na ve patients was reduced by ~80 m PIPELINE

EYP-1901 14 | EYEPOINT PHARMACEUTICALS OCT - ocular coherence tomography

Study performed by Tyrogenex

Oral vorolanib clinical activity in wet AMD Phase 2 trial Less rescue vs placebo for all doses with no ocular toxicity PIPELINE

EYP-1901 Strict pre-defined rescue criteria with anti-VEGF therapy

Any increase in fluid on OCT compared to screening visit 2 (~14 days after an IVT injection)

New or increased macular hemorrhage by fundus photography

In the placebo group, 12.5% of subjects with unilateral disease at baseline developed exudative AMD in their fellow eyes by 52 weeks, compared with 3.8% (1/26), 0%(0/27) and 0%(0/23) in the 50 mg, 100 mg, and 200 mg groups, respectively.

* Normalized for number of months on study

Study performed by Tyrogeix 15 | EYEPOINT PHARMACEUTICALS

6-month rabbit GLP toxicology completed with no unexpected safety findings

Efficacy and preliminary safety study completed in a laser CNV mini pig model

Results: dose-related activity and no observed toxicity

Non-GLP rabbit PK and safety study demonstrated drug levels in vitreous and retina/choroid significantly above the IC50 for VEGFR2

EYP-1901 pre-clinical results PIPELINE

EYP-1901 16 | EYEPOINT PHARMACEUTICALS CNV- choroidal neovascularization

GLP - good laboratory practice

PK - pharmacokinetics

In-vivo cumulative % release of vorolanib in rabbits measured over ~8 months PIPELINE

EYP-1901 17 | EYEPOINT PHARMACEUTICALS R2 for both doses indicates zero order release of drug at different dosing levels

EYP-1901 Phase 1 Trial 18 | EYEPOINT PHARMACEUTICALS

29 | EYEPOINT PHARMACEUTICALS 1-2 weeks following last injection RESULTS ENROLLMENT DOSE A DOSE B DOSE C

Open label, dose escalation, no control arm (results to be monitored on an ongoing basis)

Rescue with anti-VEGF therapy if necessary

Patients with wet AMD responsive to previous anti-VEGF therapy

12 month readout PIPELINE

Primary endpoint is safety. Secondary endpoints are BCVA and central subfield

Phase 1 DAVIO wet AMD clinical trial design

Phase 1 DAVIO wet AMD clinical trial underway with interim data expected in Q4 2021 PIPELINE

EYP-1901 1H 2021 2H 2021 PHASE 1 TRIAL PRELIMINARY RESULTS EXPECTED IN Q4 2021 FIRST PATIENT DOSED 20 | EYEPOINT PHARMACEUTICALS UPDATE

Enrollment completion announced May 25, 2021

17 patients in total dosed with EYP-1901

Positive 30-day safety results across all cohorts

On track for Q4 interim data read-out ENROLLMENT COMPLETE

17 patients enrolled across three dose cohorts

No SAEs, ocular or systemic, were reported

No reported adverse events related to intraocular inflammation

No reported adverse events related to BCVA reduction

No reported adverse events related to elevation of IOP

No events of endophthalmitis, retinal detachment or migration into the anterior chamber reported

The three subjects in Cohort 1 have been followed a minimum of six months with no reported SAEs

Positive 30-day safety results across all dose cohorts PIPELINE

EYP-1901 21 | EYEPOINT PHARMACEUTICALS SAEs - serious adverse events

BCVA - best corrected visual acuity

IOP - intraocular pressure

FDA Approved Commercial Products 22 | EYEPOINT PHARMACEUTICALS

Approved for the treatment of chronic non-infectious uveitis affecting the back of the eye Commercially launched in U.S. in 2019

Patent protection to August 2027