Good morning and welcome to Ocugen's first quarter 2024 financial results and business update. Please note that this call is being recorded at this time. All participant lines are in listen-only mode. Following the speaker's commentary, there will be a question-and-answer session. I will now turn the call over to Tiffany Hamilton, Ocugen's Head of Corporate Communications. You may begin. Thank you, operator, and good morning, everyone. Joining me on today's call and webcast is Dr. Shankar Musunuri, Ocugen's Chairman, CEO, and Co-founder, who will provide a business update and an overview of our clinical and operational progress. Michael Breininger, our Corporate Controller, is also on the call to provide a financial update for the quarter ended March 31st, 2024. Dr. Arun Upadhyay, Chief Scientific Officer, Head of Research and Development, and Dr. Huma Qamar, Chief Medical Officer, will be available to answer questions following the presentation. This morning we issued a press release detailing associated business and operational highlights for the first quarter of 2024. We encourage listeners to review the press release, which is available on our website at ocugen.com. This call is being recorded, and a replay with the accompanying slide presentation will be available on the investors section of the Ocugen website for approximately 45 days. This presentation contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, which are subject to risks and uncertainties. We may in some cases use terms such as predicts, believes, potential, proposed, continue, estimates, anticipates, expects, plans, intends, may, could, might, will, should, or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. Such statements include but are not limited to statements regarding our clinical development activities and related anticipated timelines. Such statements are subject to numerous important factors, risks, and uncertainties, and may cause actual events or results to differ materially from our current expectations. These and other risks and uncertainties are more fully described in our periodic filings with the Securities and Exchange Commission, the SEC, including the risk factors described in the section entitled "Risk Factors" in the annual reports that we file with the SEC. Any forward-looking statements that we make in this presentation speak only as of the date of the presentation. Except as required by law, we assume no obligation to update forward-looking statements contained in this presentation, whether as a result of new information, future events, or otherwise after the date of this presentation. Finally, Ocugen's quarterly report Form 10-Q covering the first quarter of 2024 has been filed. I will now turn the call over to Dr. Musunuri. Thank you, Tiffany, and thank you all for joining us today. As detailed in our press release, we are excited to discuss the substantial progress of our game-changing modifier gene therapy platform. By using nuclear hormone receptors to restore homeostasis in the retina, modifier gene therapy has the potential to address multiple inherited retinal diseases as well as larger multifactorial diseases such as dry age-related macular degeneration through a gene-agnostic approach. Just after the close of the first quarter of this year, we announced that the FDA cleared our IND application for the OCU400 phase III liMeliGhT clinical trial, and the EMA provided acceptability of the US-based trial for submission of a market authorization application. I will discuss the significance of these milestones and the potential for OCU400 in greater depth later in the presentation. OCU410 and OCU410-ST are now in phase I/II clinical trials, targeting geographic atrophy secondary to dry age-related macular degeneration and Stargardt disease, respectively, with the clinical updates expected in the third quarter of 2024. Our cell therapy platform is poised to advance with the renovations to our existing facility completed earlier this year. This gives Ocugen the capability to support NeoCart, autologous cell therapy, manufacturing for personalized phase III clinical material contingent upon adequate funding. Finally, OCU500 will soon advance into a phase I clinical trial via the National Institute of Allergy and Infectious Diseases, NIAID-sponsored trial, comparing the administration of OCU500 via two different mucosal routes: inhalation into the lungs and as a nasal spray. With three gene therapy candidates to treat blindness diseases in the clinic and a phase III ready cell therapy candidate, we are confident that 2024 will be a bellwether for Ocugen. We are thrilled to share significant advancements in our leading modifier gene therapy candidate, OCU400, as it makes remarkable strides in clinical development. The green light from the FDA to begin the phase III clinical trial marks a pivotal milestone as OCU400 becomes the first gene therapy to progress to phase III trials with such a broad Retinitis Pigmentosa indication. Until now, there has been only one marketed product to treat one of the 100 gene mutations associated with RP. Now there is real hope for all RP patients who haven't had a treatment option. Our completion of enrollment and dosing in phase I/II trial demonstrated promising safety and efficacy across various genetic mutations and dosage levels, paving the way for phase III clinical trials. OCU400 has already received key regulatory approvals, including orphan drug, regenerative medicine advanced therapy, and orphan medicinal product designations from both FDA and the European Commission for treating inherited retinal diseases. These endorsements highlight OCU400's broad therapeutic potential, and we remain on track to meet 2026 BLA and MAA approval targets. We expect to begin dosing patients in the phase III liMeliGhT clinical trial in the second quarter of 2024, which will include 150 subjects across two arms, one with patients affected by RHO mutation and one arm that is gene-agnostic. Luminance-dependent navigation assessment, LDNA, the primary endpoint for the study, focuses on the proportion of responders in treated and untreated control groups achieving an improvement of at least 2 lux levels from baseline in the study eyes. The secondary endpoint will be measured by a change in low luminance visual acuity score of 0.3 LogMAR from the baseline. The effectiveness of the treatment will be compared to an untreated control group for the secondary endpoint as well. Additionally, leveraging a dual-track strategy, we plan to expand the phase III trial in the later half of 2024 to include patients with Leber congenital amaurosis, LCA, contingent on favorable results from phase I/II study. Let me take a moment to discuss the unmet need and underserved market for RP and LCA patients. An estimated 1.6 million people globally are affected by RP and LCA combined. In the U.S. and Europe alone, our initial target markets, there are nearly 300,000 total patients. RP and LCA are classified as inherited retinal diseases from a group of heterogeneous disorders that affect the retina. These conditions frequently result in vision impairment and ultimately blindness. By establishing homeostasis in patients affected by these diseases, our aim is to preserve or improve vision. By actively sharing our insights at pertinent medical conferences and engaging with advocacy groups, we strive to raise awareness of the desperate need to find a solution for all RP and LCA patients, as well as the potential of modifier gene therapy to revolutionize treatment. To better understand the experience of one of our phase I/II clinical trial patients, I encourage you to watch his video in the patient section of our website. Moving on to our development in the treatment of geographic atrophy secondary to dry age-related macular degeneration, dAMD, and Stargardt disease with our OCU410 and OCU410-ST programs. These modifier gene therapies leverage the nuclear receptor gene, RAR-related orphan receptor A, RORA, aiming to provide a potential one-time therapy for life with a single subretinal injection. OCU410, specifically designed to address multiple pathways implicated in the pathogenesis of dAMD, offers a distinct advantage over current treatments that target only one cause of GA and often require multiple injections per year, accompanied by various safety concerns. Our approach with OCU410 is to provide a comprehensive and durable solution, a potential one-time therapy for life. Dry AMD affects about 19 million people in the US and Europe combined, while GA affects about 2-3 million people in the US and Europe, a significant market opportunity. In December 2023, we began the Phase I/II ArMaDa clinical trial for OCU410. Considerable progress has been made with the completion of dosing in both the first and second cohort, low and medium doses. Following the successful dosing in these cohorts, the Data and Safety Monitoring Board, DSMB, will convene later this month to evaluate proceeding with the high-dose cohort in the ongoing dose escalation phase of the study. After completion of the third cohort, we will transition into phase II clinical trial, the expansion phase. A key upcoming event for this trial is a clinical update, which is anticipated in the third quarter of 2024. This data will provide initial insights into the safety and efficacy of OCU410. OCU410 phase I study is multi-center and open-label, focusing on dose ranging, while phase II is randomized, aiming to expand our understanding of drugs' efficacy and safety compared to a controlled, untreated arm, with patients randomized in a 1:1:1 ratio across two dosage groups and one control group. Participants must be aged 50 or older, have a best-corrected visual acuity of approximately 24 letters or more using the ETDRS chart, and have a total geographic atrophy area between 2.5-20.5 millimeters squared. We now turn to OCU410-ST, which received orphan drug designation from the FDA for the treatment of ABCA4-associated retinopathies, including Stargardt disease. Stargardt affects approximately 100,000 people in the US and EU combined. This modifier gene therapy candidate also utilizes the RORA gene, and the Phase I/II GARDian trial for Stargardt disease is actively enrolling patients. We have completed dosing in the first cohort, low dose. In April 2024, the Data and Safety Monitoring Board approved the continuation to the medium dose phase, which we expect will be completed this month. A clinical trial update for OCU410-ST is also anticipated in the third quarter of 2024. The phase I/II trial involves up to 42 participants, 30 adults, and 12 children, which exhibit mild to moderate disease symptoms. The study uses a 3+3 dose escalation design in phase I, segmenting subjects into low, medium, and high-dose cohorts. Following the dose escalation phase, the trial will transition into phase II, the expansion phase. This expansion phase will use a 1:1:1 design to randomize subjects into two different treatment groups at varying dose levels or a controlled, untreated group, allowing for a comprehensive assessment of treatments' efficacy across different dosages. Our work across OCU400, OCU410, and OCU410-ST affirms our enduring commitment to the success of these modified gene therapies for the benefit of patients faced with the terrible prospect of losing their sight. We are encouraged by the progress in these trials and look forward to sharing further updates as we reach critical milestones and get closer to addressing substantial unmet medical needs. With that, I will now turn the call over to our Corporate Controller to provide an update on our financial results for the first quarter ended March 31st, 2024. Mike? Thank you, Shankar. Our research and development expenses for the quarter ended March 31st, 2024, were $6.8 million compared to $10.2 million for the first quarter of 2023. General and administrative expenses for the quarter ended March 31st, 2024, were $6.4 million compared to $8.3 million during the same period in 2023. Net loss was approximately $11.9 million or $0.05 net loss per share for the quarter ended March 31st, 2024, compared to a net loss of approximately $17.3 million or $0.08 net loss per share for the first quarter of 2023. Our cash and cash equivalents totaled $26.4 million as of March 31st, 2024, compared to $39.5 million as of December 31st, 2023. As always, we are constantly exploring strategic and shareholder-friendly opportunities to increase our working capital. That concludes my update for the quarter. Tiffany, back to you. Thank you, Mike. We will now open the call for questions. Operator? Thank you. We will now begin the question-and-answer session. If you have dialed in and would like to ask a question, please press star 1 on your telephone keypad to raise your hand and join the queue. If you would like to withdraw your question, simply press star 1 again. If you are called upon to ask your question in our listening via loudspeaker on your device, please pick up your handset and ensure that your phone is not on mute when asking your question. Again, press star 1 to join the queue, and your first question comes from the line of Arthur He with H.C. Wainwright. Please go ahead. Hey, good morning, Shankar and team. Congrats on the progress. So I just had a quick one regarding the 400 phase III study. For the gene-agnostic arm, is there a minimum number of patients for each specific gene mutation to meet the requirement for the BLA application? Hey, Arthur, good morning. I'll let Arun take the response. No, we have not pre-specified any specific number of patients for each mutation, but our approach is going to be to include as many mutations as possible in the gene-agnostic arm. Okay, thanks. Thanks for the color. And also, my second question is regarding the 200. Could you give us more color on the status and what's your effort to get the clinical hold lifted as soon as possible? Yes, so we are working on addressing the CMC question we received from FDA, and we are planning to address that, ASAP, and then continue the development of OCU200 further. Okay, great. Thanks for taking my question. Thank you, Arthur. Your next question comes from Robert LeBoyer with Noble Capital Markets. Please go ahead. Good morning and congratulations on all the progress during the quarter. My question has to do with the phase III trial coming up, and you had mentioned some milestones to start. Are there any timeframes or any particular milestones that we can look forward to in terms of accrual or projected time for data release? Yeah. Robert, I'll let Dr. Qamar answer the question. Hi, thank you for your question. In terms of the milestones, as you're aware, that OCU400 has recently got approval. We are currently screening patients, and we will be continuously updating the market with dosing updates very soon. Okay, is there any projected time for the first data release? For OCU400, phase III or phase I/II? Either, actually. Okay. So phase I/II, we have already updated that. Continuous updates will be coming in the next quarter as well, and as soon as we receive more data on the LCA patients. For OCU400 phase III, there is no timeframe, as it will be periodic, and we will be giving periodic updates to the market as soon as it's available. And Robert, I think this is a controlled clinical trial, phase III. So until the study is done, we cannot reveal any information to the market on the efficacy portion of it. Sure. That's probably. We'll provide periodic updates, as Dr. Qamar is saying, on recruitment and where the trial is going, and also give markets an update about on track for our target approval for BLA and MAA in 2026. Okay. Yeah, that's probably as much as anyone can say for a rare disease like this, so thank you. Your next question comes from the line of Daniil Gataulin with Chardan. Please go ahead. Yeah, hey, good morning, guys. Thank you for taking the question. Also, a question on OCU400 and phase III. So you mentioned that as part of liMeliGhT strategy, you will be expanding phase III to include patients with LCA pending the phase I/II to LCA data. I just wanted to clarify, this will be added as a new arm in the trial or if it will be a separate standalone trial? And I guess the second part of the question is, what data from LCA phase I/II would you consider favorable that would give you a go-ahead decision for these patients? Thank you. Arun, we'll take the call. Thanks. Thanks, Shankar. Yeah, so based on the phase I/II study outcome, our plan is to have the separate trial for the LCA because it's a different disease. Once we have the data available, we'll be engaging with the agency, and based on the agency recommendation, we will initiate the trial accordingly. Okay, got it. Thank you. In terms of the phase I/II data threshold, what would you consider favorable to advance into phase III? Primarily the safety and efficacy. Okay. All right. Thank you. This concludes the Q&A portion. I will now turn the call back over to Chairman and CEO Dr. Shankar Musunuri. Thank you, Operator. Our efforts in the first quarter of the year evidence the importance of our gene therapy programs and the need to operate the business to ensure their success. We are opportunistic about Ocugen cell therapy and vaccine platforms, knowing that these technologies have great therapeutic and financial potential, and are pursuing partnerships to support our entire pipeline. We look forward to what this quarter and the rest of the year holds for the company, our people, and the patients we serve. Tiffany? Thanks, everyone. Bye. Ladies and gentlemen, that concludes today's call. Thank you all for joining. You may now disconnect.