RegCell Rakes In $66 Million Series A

<p><strong>EMERYVILLE<&sol;strong> &&num;8212&semi; RegCell&comma; Inc&period;&comma; a biotechnology company developing first-in-class therapies to restore immune tolerance&comma; has closed a fully subscribed Series A financing and a second non-dilutive grant from Japan’s Agency for Medical Research and Development &lpar;AMED&rpar;&comma; totaling &dollar;66 million&period; The funding will advance RegCell’s epigenetic reprogramming platform&comma; built on Nobel Laureate and RegCell co-founder Professor Shimon Sakaguchi’s discovery of regulatory T cells &lpar;Tregs&rpar;&comma; into clinical-stage development across multiple autoimmune indications&period;<&sol;p>&NewLine;<p>&OpenCurlyDoubleQuote;For decades&comma; my research has centered on the question of how the immune system governs itself&comma;” says Dr&period; Sakaguchi&comma; whose pioneering research led to the discovery of Tregs’ essential function in maintaining immune tolerance&period; &OpenCurlyDoubleQuote;To see this platform carry that discovery toward patients is deeply meaningful to me after all these years&period;”<&sol;p>&NewLine;<p>Unlike conventional immunosuppressants&comma; which have remained the standard of care for autoimmune diseases for decades&comma; RegCell’s platform distinguishes disease-causing immune cells from healthy ones&period; Rather than broadly dampening immune function and leaving patients vulnerable to serious infections&comma; cardiac toxicity&comma; and secondary malignancies&comma; RegCell’s approach converts pathogenic T cells into stable&comma; epigenetically reprogrammed&comma; disease-relevant Tregs that restore immune tolerance at the source&period;<&sol;p>&NewLine;<p>Existing autoimmune therapies work by broadly suppressing the immune system with actions ranging from blocking cytokines to impeding trafficking to depleting immune cells&period; RegCell’s platform is designed to instead restore immune tolerance through a durable&comma; targeted mechanism upstream of conventional approaches&comma; converting the specific T cells driving disease into regulatory T cells that can restore immune tolerance while preserving normal immune function&period;<&sol;p>&NewLine;<p>&OpenCurlyDoubleQuote;We believe that patients need better options than what current autoimmune therapies provide&comma;” said Michael V&period; McCullar&comma; Ph&period;D&period;&comma; MBA&comma; President and CEO of RegCell&period; &OpenCurlyDoubleQuote;With this financing and AMED’s continued support&comma; we intend to rapidly advance our epigenetic reprogramming platform into the clinic&comma; establish proof of concept in patients&comma; and expand its potential across autoimmune disease&period;”<&sol;p>&NewLine;<p>Led by Playground Global&comma; the &dollar;44 million Series A financing was joined by other new investors including Global Brain&comma; Mitsui Chemicals&comma; LG Technology Ventures&comma; Alumni Ventures&comma; and Medical Incubator Japan&comma; and was supported by existing investors including Fast Track Initiative&comma; The University of Tokyo Edge Capital Partners &lpar;UTEC&rpar;&comma; Osaka University Venture Capital&comma; and Kyoto iCAP&period; As part of this financing&comma; Jory Bell&comma; General Partner at Playground Global&comma; will join RegCell’s Board of Directors&period;<&sol;p>&NewLine;<p>&OpenCurlyDoubleQuote;RegCell is pursuing something genuinely novel in autoimmune disease&colon; instead of chasing a single target&comma; the company’s approach reprograms a patient’s own auto-reactive T cells to reset the immune system on its own terms&comma;” said Jory Bell&comma; General Partner at Playground Global&comma; and RegCell Board Member&period; &OpenCurlyDoubleQuote;The company has the potential to move beyond symptom management toward something closer to a cure for conditions like myasthenia gravis&comma; rheumatoid arthritis and ulcerative colitis&period;”<&sol;p>&NewLine;<p>In addition to the Series A financing&comma; RegCell was awarded an additional approximately &dollar;22 million in non-dilutive funding &lpar;¥3&period;4 billion&rpar; from AMED&period; This funding will accelerate the second generation of RegCell’s epigenetic reprogramming platform to convert pathogenic T cells into lineage-stable antigen-specific Tregs&comma; as well as the strategic expansion of RegCell’s clinical pipeline through an additional Phase 2 proof-of-concept study&period;<&sol;p>&NewLine;<p>This milestone marks RegCell’s second AMED award&comma; bringing AMED’s total commitment of non-dilutive capital for RegCell to approximately &dollar;59&period;3 million &lpar;¥9&period;0 billion&rpar;&period; RegCell was first awarded approximately &dollar;37&period;3 million &lpar;¥5&period;6 billion&rpar; in non-dilutive capital from AMED in 2024 to develop the first generation of its epigenetic reprogramming platform through clinical proof-of-concept in autoimmune liver diseases&period;<&sol;p>&NewLine;<p>&OpenCurlyDoubleQuote;Our conviction is that restoring immune tolerance through Treg biology could meaningfully change how autoimmune disease is treated&period; We look forward to building alongside Playground and RegCell’s team as it moves toward the clinic&comma;” said Koji Yasuda&comma; Principal at Fast Track Initiative and Board Director at RegCell&period;<&sol;p>&NewLine;

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