
Eyestem Secures Funding to Advance Eyecyte-RPE Phase 2 Clinical Trial
You're reading Entrepreneur India, an international franchise of Entrepreneur Media.
Eyestem Research Pvt Ltd has secured funding from existing investors along with a new strategic partner in a significantly oversubscribed round.
The proceeds will be directed towards completing the ongoing Phase 2 clinical trial of its retinal pigment epithelial cell therapy, Eyecyte-RPE™, in India and preparing for an Investigational New Drug application with the United States Food and Drug Administration.
Dr Jogin Desai, Founder and Chief Executive Officer of Eyestem, said, "Strong participation by internal investors and addition of a strategic investor underline the shared belief in Eyestem's long-term vision of creating an innovative cell therapy platform providing scalable solutions for incurable diseases worldwide. This USD 10 million fundraise will support the next leg of development and strengthen the foundation for global expansion. We continue to prioritise rigorous clinical progress and the capabilities needed to ensure global patient access to this therapy."
Raju Barwale, Chairman of Mahyco, and Sandeep Singh, Managing Director of Alkem Laboratories Ltd, stated, "Eyestem's pioneering treatment is delivering remarkable outcomes that set a new benchmark in ophthalmic cell therapy. The results observed in Phase 1 not only demonstrate promising efficacy compared to other ongoing global trials but also validate India's potential as a leader in advanced cell therapy innovations. We are privileged to support a breakthrough that has the potential to redefine treatment outcomes for millions suffering from dry AMD."
Eyecyte-RPE™ is intended for patients with geographic atrophy, a severe stage of dry age-related macular degeneration. In the completed Phase 1 trial involving patients with advanced disease and severe vision loss, the therapy demonstrated a strong safety profile with no serious adverse events and showed early clinical benefits. These included an average improvement of 15.8 letters in six patients over six months and an average improvement of 11 letters in two patients over one year. The Phase 2 trial will assess the product in a larger group of patients with moderate disease.
Founded by Dr Jogin Desai and a team of experts with decades of experience in pharmaceutical product development, retinal surgery, and cell biology, Eyestem is headquartered in Bengaluru and Delaware. Its proprietary Eyecyte-RPE™ therapy is derived from human induced pluripotent stem cells and is designed to replace damaged retinal cells, offering potential regeneration of diseased tissue.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


The Hill
29 minutes ago
- The Hill
Trump's chip deal raises legal questions
The two firms have agreed to share 15 percent of the revenue generated from selling advanced artificial intelligence (AI) chips to China in order to secure export licenses after a months-long pause, a U.S. official confirmed to The Hill on Monday. 'It's bizarre in many respects and pretty troubling because Congress didn't have anything to say about this,' said Gary Hufbauer, a nonresident senior fellow at the Peterson Institute for International Economics. 'It's just the president's own negotiating with the individual companies,' he continued. 'That's not how, historically, we've done business in this country.' Under the agreement, Nvidia will share 15 percent of its revenue from H20 chip sales to China, while AMD will share the same portion of its MI308 chip sales. Both of the Nvidia and AMD chips in question, which are graphics processing units (GPUs) designed for the Chinese market with U.S. export controls in mind, faced new restrictions from the Trump administration in April, effectively blocking sales to China. Last month, Nvidia and AMD said the U.S. government had assured them it would begin approving export licenses for the H20 and MI308 chips, although the Commerce Department reportedly did not start issuing licenses for several weeks. The new revenue-sharing agreement comes after Nvidia CEO Jensen Huang met with President Trump at the White House last week, according to Bloomberg. Huang has found himself in a tricky situation, balancing Washington and Beijing's interests as both countries vie for AI dominance. The agreement appears to remove a major impediment for both companies. Nvidia said earlier this year it incurred $4.5 billion in charges associated with the chip restrictions in the first quarter and expected an $8 billion sales hit in the second quarter. AMD forecast a $1.5 billion hit to revenue this year. The deal represents a notable shift in how the government approaches export controls. 'It's quite extraordinary because it turns the export control function of the government into a money-raising proposition, and that's never happened before,' Hufbauer said.
Yahoo
an hour ago
- Yahoo
Market Minute 8-11-25- Nvidia, AMD Govt. "Rev Share" in Focus
After a solid end to last week, stocks are gaining a bit more ground in early trading today. Crude oil is up with the dollar, while gold and silver are lower and Treasuries are flattish. To get more articles and chart analysis from MoneyShow, subscribe to our .) The Trump Administration continues to find new and novel ways to extract revenue in exchange for trade concessions. The latest: Nvidia Corp. (NVDA) and Advanced Micro Devices Inc. (AMD) will do a 'revenue share' deal with the US government, giving it 15 cents of every dollar in sales they get selling H20 and MI308 chips to Chinese customers. That kind of ultra-targeted export levy is highly unusual, but it follows several other targeted tariffs on imports of various semiconductors, metals, and other products. While neither of those chips are the most advanced ones NVDA and AMD sell, they can still be used to help with Artificial Intelligence (AI) model training and other tasks. NVDA and AMD shares were slightly lower on the news. NVDA, AMD, LIT, PSKY (YTD % Change) Data by YCharts Global lithium stocks are rallying thanks to an 'anti-involution' push in China. In short, the Chinese government is trying to eliminate production overcapacity and deflation in materials like lithium, sectors like steel, and industries like e-commerce and Electric Vehicles (EVs). As part of that trend, the battery giant Contemporary Amperex Technology Co. Ltd., or CATL, said it would shut down its massive Jianxiawo lithium mine for at least three months. That mine accounts for about 6% of worldwide lithium output. Others in the area account for another 5% of output. If more close, it will accelerate the elimination of a lithium supply glut and boost returns for Western mine operators. Chinese lithium futures surged by the daily limit of 8% Monday, while the Global X Lithium & Battery Tech ETF (LIT) was recently trading up by about 6%. See also: NJR: A Higher-Yielding Nat Gas Utility Stock Fresh off the closure of an $8 billion merger and rebranding as Paramount Skydance Corp. (PSKY), the media conglomerate said it would buy the rights to UFC live fighting events for $7.7 billion. The seven-year deal kicks in for 2026 when a current pay-per-view deal between UFC and ESPN expires. Subscribers to Paramount+ will then be able to watch 13 marquee events plus 30 'Fight Nights' at no additional charge. More From LHX: A "Triple Beat" Earnings Play in the Defense Sector MGK and IGM: Two QQQ Alternatives for Tech Investors to Consider Market Minute 8/8/25: Gold Flirts with Fresh Highs Amid Tariff Turmoil


Business Wire
2 hours ago
- Business Wire
FDA Grants 510(k) Clearance for Sonic Incytes' Velacur ONE™, AI-Guided Point of Care Ultrasound for the Management of Chronic Liver Diseases
VANCOUVER, British Columbia--(BUSINESS WIRE)--Sonic Incytes Medical Corp, proudly announces that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for Velacur ONE™, its point-of-care ultrasound elastography device. Building on the success of its original model, Velacur™, Velacur ONE™ introduces an enhanced interface and features for improved portability and user experience. These improvements enable broader scalability to support Sonic Incytes' accelerated US and global expansion strategy. Velacur ONE™ measures attenuation, VDFF (Velacur Determined-Fat Fraction), and liver stiffness using 3D S-WAVE and aids in the management of chronic liver disease including MASH and MASLD. The launch of Velacur ONE™ marks a pivotal milestone for Sonic Incytes as we accelerate our US and global commercial expansion strategy. Share Velacur ONE™ arrives at a critical time for improved non-invasive testing, following the recent FDA clearance of Rezdiffra—the first therapeutic for Metabolic dysfunction–associated steatohepatitis (MASH), a progressive and often underdiagnosed liver disease. In the U.S. alone, an estimated 100 million adults have Metabolic dysfunction–associated Steatotic Liver Disease (MASLD)1, with 15–20 million of those affected by MASH2. Yet, 90% of MASH cases remain undiagnosed3. If left untreated, worsening MASH increases morbidity and may progress to severe complications, including cirrhosis, liver failure, liver cancer, and liver transplant4,5. MASH remains challenging to diagnose effectively due to the limitations of existing non-invasive methods, especially those available at the point-of-care. With the first therapeutic now available and more in the pipeline, clinicians need improved non-invasive tests to diagnose and monitor MASH at point-of-care6. Current treatment guidelines for MASH recommend imaging-based elastography, such as Velacur™, to assess liver scarring (fibrosis) and fat content (steatosis). While ultrasound elastography is widely used, when it comes to treating patients with MASH, liver stiffness alone cannot be relied on to assess treatment response in the short term7. The best predictor of treatment responses was a decrease in steatosis (identified as ≥30% reduction in MRI-PDFF)8. VDFF, Sonic Incytes' proprietary algorithm that received FDA clearance in 2024, demonstrates a strong correlation (r = 0.85) with MRI-PDFF—the gold standard for liver fat measurement—and achieves an outstanding accuracy (AUC) of 95% of patients with more than 5% MRI-PDFF, defining the presence of hepatic steatosis9. Velacur ONE™ combines this technology with a refined user interface, including B-mode imaging—enabling 3–4x higher reimbursement than non-imaging elastography—and an AI-based organ overlay feature to aid in liver localization, making it the only point-of-care device that estimates both liver stiffness and attenuation that correlates to MRI-PDFF10. 'The launch of Velacur ONE™ marks a pivotal milestone for Sonic Incytes as we accelerate our US and global commercial expansion strategy,' said Barry Allen, CEO of Sonic Incytes. 'This next-generation device enhances clinical utility and operational scalability, positioning us to better support the growing demand for accessible, non-invasive liver diagnostics and treatment, particularly in the management of MASLD and MASH at the point-of-care.' About Sonic Incytes Sonic Incytes is committed to enhancing patient care through innovative diagnostic solutions. The company's flagship product, Velacur™, equips physicians with an advanced liver imaging tool to help manage the growing epidemic of fatty liver disease. Velacur™ offers real-time, AI-guided quantification of the key markers for fatty liver disease: liver stiffness, attenuation and VDFF. With real-time results, a low up-front cost and AI guidance, Velacur™ makes liver imaging at the point-of-care affordable and accessible. For more information, visit ________________________________ 1 American Liver Foundation. (2025, June). Nonalcoholic fatty liver disease (NAFLD). American Liver Foundation 2 Le P, Tatar M, Dasarathy S, et al. Estimated Burden of Metabolic Dysfunction–Associated Steatotic Liver Disease in US Adults, 2020 to 2050. JAMA Netw Open. 2025;8(1):e2454707. doi:10.1001/jamanetworkopen.2024.54707 3 Fishman, J., Kim, Y., Charlton, M.R. et al. Estimation of the Eligible Population For Resmetirom Among Adults in the United States for Treatment of Non-Cirrhotic NASH with Moderate-to-Advanced Liver Fibrosis. Adv Ther 41, 4172–4190 (2024). 4 Friedman SL. Fat, fibrosis, and the future: navigating the maze of MASLD/MASH. J Clin Invest. 2025 Apr 1;135(7):e186418. doi: 10.1172/JCI186418. PMID: 40166940; PMCID: PMC11957683. 5 Fishman J, Alexander T, Kim Y, Kindt I, Mendez P. A clinical decision support tool for metabolic dysfunction-associated steatohepatitis in real-world clinical settings: a mixed-method implementation research study protocol. J Comp Eff Res. 2024 Oct;13(10):e240085. doi: 10.57264/cer-2024-0085. Epub 2024 Sep 20. PMID: 39301878; PMCID: PMC11426282. 6 Gbadamosi, S. O., Evans, K. A., Brady, B. L., & Hoovler, A. (2025). Noninvasive tests and diagnostic pathways to MASH diagnosis in the United States: a retrospective observational study. Journal of Medical Economics, 28(1), 314–322. 7 Noureddin, M., Charlton, M. R., Harrison, S. A., Bansal, M. B., Alkhouri, N., Loomba, R., Sanyal, A. J., & Rinella, M. E. (2024). Expert panel recommendations: Practical clinical applications for initiating and monitoring resmetirom in patients with MASH/NASH and moderate to noncirrhotic advanced fibrosis. Clinical Gastroenterology and Hepatology, 22(12), 2367–2377. 8 Chen VL, Morgan TR, Rotman Y, Patton HM, Cusi K, Kanwal F, Kim WR. Resmetirom therapy for metabolic dysfunction-associated steatotic liver disease: October 2024 updates to AASLD Practice Guidance. Hepatology. 2025 Jan 1;81(1):312-320. doi: 10.1097/HEP.0000000000001112. Epub 2024 Oct 18. Erratum in: Hepatology. 2025 Apr 1;81(4):E133. 9 Honarvar, M., Lobo, J., Schneider, C., Klein, S., Smith, G. I., Loomba, R., Ramji, A., Hassanein, T., Yoshida, E. M., Pang, E., Curry, M. P., & Afdhal, N. H. (2024). Methods and validation of Velacur determined fat fraction in patients with MASLD. WFUMB Ultrasound Open, 2(2), Article 100061. Expand