OOrna Therapeutics develops RNA-based therapies using engineered circular RNA (oRNA) to treat diseases. Its approach uses circular RNA instead of linear RNA for potentially longer-lasting expression, delivered in vivo via lipid nanoparticles to target cells where the oRNA encodes therapeutic proteins or receptors like CARs. Its platform aims for in situ CAR therapy and expansions across cancer, regenerative medicine, protein replacement, infectious diseases, and autoimmunity, with delivery that may simplify treatment logistics compared with ex vivo methods. The goal is to develop and commercialize oRNA therapeutics, advance regulatory approvals, and form collaborations to bring RNA medicines to patients.
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Industries
Company Size
51-200
Company Stage
Acquired
Total Funding
$321M
Headquarters
Cambridge, MA
Founded
2019
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Total Funding
$321M
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CRISPR Therapeutics announces the appointment of Siva Sakhamuri, Ph.D., as Chief Technical Officer. ZUG, Switzerland and BOSTON, Nov. 02, 2026 (GLOBE NEWSWIRE) - CRISPR Therapeutics (Nasdaq: CRSP), today announced the appointment of Sivakesava (Siva) Sakhamuri, Ph.D., as Chief Technical Officer, effective immediately. Dr. Sakhamuri brings about 30 years of technical operations and manufacturing leadership experience across biologics, vaccines, oligonucleotides, RNA therapeutics and lipid nanoparticle (LNP) delivery. "Siva has tremendous experience advancing novel therapies across various modalities into the clinic all the way through commercial stage, with expertise spanning biologics, RNA therapeutics and vaccines," said Samarth Kulkarni, Ph.D., Chairman and Chief Executive Officer of CRISPR Therapeutics. "It is exciting to have Siva join our leadership team as we advance both our gene editing and RNA therapies into late-stage clinical development." "CRISPR Therapeutics has built a broad pipeline and strong in-house manufacturing capabilities, and I am excited to join at this stage of the Company's growth," said Dr. Sakhamuri. "I look forward to working with the talented team to scale our technical operations and manufacturing organization as we work to bring these investigational therapies to patients." Dr. Sakhamuri joins CRISPR Therapeutics from Orna Therapeutics, where he served as Chief Technical Officer since 2024, leading the CMC and quality organizations supporting the company's circular RNA LNP programs through its acquisition by Eli Lilly and Company in 2026. Previously, he served as Senior Vice President and Head of Technical Operations and Quality at Omega Therapeutics, where he built the process development, analytical development, manufacturing, supply chain and quality functions and supported the company's first Investigational New Drug (IND) application and Clinical Trial Application (CTA) clearances for an mRNA LNP program. From 2016 to 2021, he was Vice President, Manufacturing at Alnylam Pharmaceuticals, where he led CMC readiness for the commercial launch of three RNA interference (RNAi) therapeutics, oversaw internal and external manufacturing operations, and managed the construction of an internal oligonucleotide manufacturing facility. Earlier in his career, Dr. Sakhamuri held leadership roles of increasing responsibility at Alexion Pharmaceuticals, where he led global technology transfer, technical services, and process and analytical development functions; Sanofi Pasteur, where he managed a commercial vaccine manufacturing operations; and Bristol Myers Squibb, where he held roles in biologics process development and manufacturing. Over his career, he has managed or supported 10 Biologics License Application (BLA) and New Drug Application (NDA) submissions and nine IND applications, and contributed to eight product launches. Dr. Sakhamuri received his Ph.D. in Biochemical Engineering from the Indian Institute of Technology, Chennai. About CRISPR Therapeutics CRISPR Therapeutics is a leading biopharmaceutical company focused on developing transformative gene-based medicines for serious human diseases. Founded over a decade ago as an early pioneer in CRISPR/Cas9 gene editing, the Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY(R)(exagamglogene autotemcel [exa-cel]), the world's first CRISPR-based therapy, for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia. Today, CRISPR Therapeutics is advancing a broad, diversified pipeline spanning hemoglobinopathies, cardiovascular disease, autoimmune disease, oncology, regenerative medicine and rare diseases. The Company is also expanding its gene editing toolkit through SyNTase(TM) editing, its novel, proprietary platform designed to enable precise, efficient, and scalable gene correction. To accelerate its impact, CRISPR Therapeutics has established strategic collaborations with leading biopharmaceutical partners, including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California. To learn more, visit www.crisprtx.com. Investor Contact: +1-617-307-7503 [email protected] Media Contact: +1-617-315-4493 [email protected]
Taiho Ventures, LLC celebrates 10th anniversary. PR Newswire Today at 11:00pm PDT TOKYO and MENLO PARK, Calif., April 15, 2026 /PRNewswire/ - Taiho Pharmaceutical Co., Ltd. (Taiho Pharmaceutical) and Taiho Ventures, LLC (TVL), a strategic corporate venture capital (CVC) arm of Taiho Pharmaceutical, announced on April 15 that TVL has reached its 10th anniversary since its establishment on April 15, 2016. Over the past 10 years, TVL has built strong track records: - Maintained the largest fund size among the CVC firms of the Japanese pharmaceutical industry with a focus on delivering cutting-edge technologies and therapies to society by supporting therapeutics startups while leveraging its experience in research and development and business management. - Invested in more than 30 innovative companies developing novel therapeutics and cutting-edge healthcare technologies. - Achieved multiple successful exits, including notable acquisitions such as Dren Bio (asset acquired by Sanofi), Halda Therapeutics, Inc. (acquired by Johnson & Johnson), and Orna Therapeutics, Inc. (acquired by Eli Lilly and Company), as well as several initial public offerings. - TVL's first portfolio company, Arcus Biosciences, Inc., granted Taiho Pharmaceutical exclusive licenses to five pipeline programs in certain territories, contributing to the strengthening of Taiho Pharmaceutical's research and development pipeline. Since its inception, TVL has maintained an active investment presence across the United States, Europe, and Japan, reflecting its commitment to identifying and supporting promising startups on a global scale. Its evergreen fund structure enables a patient, long-term investment approach and allows continued support for portfolio companies beyond traditional fund life cycles. *Evergreen funding provides businesses with continuous capital infusions, supporting steady growth and reducing financial stress. As it enters its second decade, TVL remains committed to creating long-term value through close collaboration with entrepreneurs and innovators and to contributing to the development of transformative healthcare technologies that address unmet medical needs. About Taiho Ventures, LLC Taiho Ventures, LLC is a strategic corporate venture capital arm of Taiho Pharmaceutical Co., Ltd., a Japanese specialty pharma focusing on oncology, allergy and immunology. Taiho Ventures is looking at early-stage preclinical oncology companies as well as platform technology companies for its core therapeutic areas. Taiho Ventures will review the wide variety of modalities for both biologics and small molecules. The company will also consider the option type of investments and spin-outs, in addition to pure equity investments. SOURCE Taiho Pharmaceutical Co., Ltd.; Taiho Ventures, LLC This is a paid placement. For further inquiries, please contact PR Newswire directly.
Eli Lilly buys Orna Therapeutics for $2.4bn: A bet on in vivo cell therapy. M&A News / Cell & Gene Therapy | Indianapolis, IN | Feb 11, 2026 Eli Lilly bets on in vivo cell therapy in $2.4bn Orna Therapeutics buyout. Deal Snapshot Acquirer Eli Lilly and Company Target Company Orna Therapeutics Transaction Value Up to $2.4 Billion Core Technology Circular RNA (circRNA) & Lipid Nanoparticles Eli Lilly joins the growing list of big pharma companies hoping to see success from their acquired in vivo CAR-T programmes. The company is acquiring in vivo cell therapy-focused biotech, Orna Therapeutics, in an immunology deal worth up to $2.4bn. Through the agreement, Lilly will gain access to Orna's new class of circular RNA (circRNA) and lipid nanoparticle-based therapies. These are designed to trigger the creation of therapeutic proteins by a recipient's immune system to treat autoimmune diseases in vivo. At the heart of this deal lies ORN-252, which Orna is developing to treat B-cell-driven autoimmune diseases by targeting the CD19 lymphocyte surface antigen. Efficacy & Differentiation: Preclinical trials on the circRNA platform have demonstrated promising efficacy signals, triggering more durable expression of therapeutic proteins than other RNA or cell therapy platforms. Orna believes this could "unlock treatments that are not feasible with current technologies." Eli Lilly's Orna acquisition follows a flurry of high-value deals in early 2026, including a $1.12bn agreement with Seamless Therapeutics and a $1.2bn acquisition of Ventyx. These moves bolster Lilly's cell and gene therapy (CGT) pipeline, which saw 27 deals signed between 2020 and 2025 according to GlobalData. This strategic expansion comes after a positive FY2025, where Lilly achieved 45% sales growth driven by its obesity portfolio. The company recently made history as the first healthcare entity to join the $1tn market cap club, alongside tech leaders like NVIDIA and Apple. In vivo cell therapies catch industry attention. As companies look to mitigate commercialisation and manufacturing (CMC) challenges, many are betting on in vivo CAR-T alternatives. Unlike traditional autologous models, in vivo therapies are less complex and expensive to manufacture. They also sidestep patient-related challenges like lymphodepletion or bridging therapies. Lilly is not alone in this pursuit. In 2025, AbbVie acquired Capstan Therapeutics for $2.1bn, Gilead's Kite Therapeutics invested $350m in Interius BioTherapeutics, and BMS merged with Orbital Therapeutics in a $1.5bn deal, all signalling a massive industry shift toward in vivo models.
Eli Lilly to acquire Orna Therapeutics in deal valued Up to $2.4 billion. Eli Lilly and Company has entered into a definitive agreement to acquire Orna Therapeutics, Inc., a biotechnology company focused on in vivo immune cell engineering using circular RNA technology. The acquisition strengthens Lilly's push into next-generation genetic medicines, particularly in vivo CAR-T therapies for autoimmune diseases - an area currently constrained by the cost and complexity of ex vivo cell therapy. Why Orna matters? Orna is developing a new therapeutic class based on: * Engineered circular RNA (oRNA) * Proprietary lipid nanoparticle (LNP) delivery systems This approach allows a patient's own body to generate cell therapies internally, potentially bypassing: * Cell extraction * Ex vivo manipulation * Re-infusion logistics Preclinical experiments suggest Orna's circular RNA platform may enable more durable protein expression than conventional linear mRNA, opening treatment possibilities not feasible with current RNA or cell therapy technologies. Lead program: in vivo CAR-T for autoimmune disease. Orna's lead asset, ORN-252, is a clinical trial-ready, CD19-targeted in vivo CAR-T therapy aimed at B cell - driven autoimmune diseases. Unlike traditional autologous CAR-T: * CAR-T cells are generated inside the patient * Manufacturing, time delays, and high costs may be significantly reduced * Broader patient access becomes feasible Lilly's strategic rationale. Lilly is targeting a known bottleneck in autoimmune CAR-T development. Dr. Francisco Ramírez-Valle, SVP and Head of Immunology Research and Early Clinical Development at Lilly, said early CAR-T studies have shown strong promise, but ex vivo approaches remain difficult to scale. He emphasized that Lilly sees Orna's platform as a way to: * Remove logistical barriers * Expand access to transformative therapies * Create an entirely new class of genetic medicines Orna's perspective. Dr. Joe Bolen, CEO of Orna Therapeutics, highlighted that the company's circular RNA and LNP platforms are designed to unlock in vivo CAR-T therapies across multiple B cell - driven autoimmune indications. He added that partnering with Lilly accelerates the ability to fully realize the technology's therapeutic potential. Deal terms at a glance. * Transaction type: Acquisition * Total potential value: Up to $2.4 billion * Structure: * Upfront cash payment * Additional milestone-based payments tied to clinical development Final accounting treatment will be determined by Lilly under GAAP and reflected in its financial results following closing. Advisors. * Legal counsel (Lilly): Paul, Weiss, Rifkind, Wharton & Garrison LLP * Financial advisor (Orna): Lazard * Legal counsel (Orna): Goodwin Procter LLP Bigger picture. This deal signals: * Lilly's serious commitment to in vivo cell therapy * Growing confidence in circular RNA as a next step beyond mRNA * A strategic shift toward scalable autoimmune CAR-T solutions If Orna's platform translates clinically, it could redefine how CAR-T therapies are delivered - moving from bespoke manufacturing to off-the-shelf, in-body generation.
Lilly acquires Orna Therapeutics to boost cell therapy innovations. Eli Lilly and Company has entered a definitive agreement to acquire Orna Therapeutics, a biotechnology firm based in Watertown, Massachusetts. This strategic acquisition, announced on February 9, 2026, aims to enhance Lilly's capabilities in cell therapy innovations, particularly focusing on treatments for B cell-driven autoimmune disorders. Lilly's acquisition of Orna Therapeutics. The agreement allows Lilly to acquire Orna for up to $2.4 billion. This total includes an upfront payment with further disbursements contingent upon the achievement of specific clinical development milestones. Lilly plans to reflect this transaction in its financial results and guidance upon closing. Innovations in cell therapy. Orna Therapeutics champions a new class of therapeutics designed with engineered circular RNA and novel lipid nanoparticles. This groundbreaking approach enables patients' bodies to create cell therapies aimed at treating underlying diseases. Orna's lead candidate, ORN-252, is a clinical trial-ready CAR-T therapy targeting CD19, which is intended for B cell-driven autoimmune diseases. * Lead Program: ORN-252 (CAR-T therapy targeting CD19) * Focus: B cell-driven autoimmune diseases * Technology: Engineered circular RNA paired with lipid nanoparticles The potential of Orna's circular RNA platform is significant. Early research indicates it may offer more durable protein expression compared to existing therapies, which could lead to novel treatment options that are not feasible with traditional RNA or cell therapies. Expert insights. Dr. Francisco Ramírez-Valle, Senior Vice President at Lilly, emphasized the promise of cell therapies for autoimmune patients. However, he acknowledged the complexity and cost associated with ex vivo treatment methods. "They make it challenging to deliver these breakthroughs to a broader patient population," he noted. The acquisition aligns with Lilly's commitment to pioneering innovative therapeutics. Joe Bolen, CEO of Orna, expressed enthusiasm about combining their technology with Lilly's expertise in patient-centric therapeutics. Corporate partnerships. In terms of legal and financial counsel, Paul, Weiss, Rifkind, Wharton & Garrison LLP represents Lilly, while Lazard is advising Orna. Goodwin Procter LLP also supports Orna in this transaction. About Lilly and Orna Therapeutics. * Lilly: A leader in scientific innovation aimed at improving global health, focusing on diseases like diabetes, Alzheimer's, and various immune disorders. * Orna Therapeutics: Focused on revolutionizing RNA medicine with their oRNA(R) technology, offering advantages in production and protein expression. This acquisition stands to significantly advance Lilly's pipeline in genetic medicine and in vivo cell engineering, ultimately aiming to provide new therapeutic solutions for patients in need.
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Industries
Company Size
51-200
Company Stage
Acquired
Total Funding
$321M
Headquarters
Cambridge, MA
Founded
2019
Find jobs on Simplify and start your career today
We update Orna Therapeutics's jobs every few hours, so check again soon!Browse all jobs