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AstraZeneca plans to invest $50 billion in America for medicines manufacturing and R&D

By News

AstraZeneca today announces $50 billion of investment in the United States by 2030, building on America’s global leadership in medicines manufacturing and R&D. This investment is expected to create tens of thousands of new, highly skilled direct and indirect jobs across the country powering growth and delivering next generation medicines for patients in America and worldwide.

The cornerstone of this landmark investment is a new multi-billion dollar US manufacturing facility that will produce drug substances for the Company’s innovative weight management and metabolic portfolio, including oral GLP-1, baxdrostat, oral PCSK9 and combination small molecule products. The new state-of-the-art centre will produce small molecules, peptides and oligonucleotides. This multi-billion dollar capital investment is in addition to the $3.5 billion announced in November 2024.

The drug substance facility, planned to be in the Commonwealth of Virginia, would be AstraZeneca’s largest single manufacturing investment in the world. The facility will leverage AI, automation, and data analytics to optimise production.

The $50 billion investment across our R&D and manufacturing footprint in the US over the next five years also includes:

  • Expansion of our R&D facility in Gaithersburg, Maryland
  • State-of-the-art R&D centre in Kendall Square, Cambridge, Massachusetts
  • Next-generation manufacturing facilities for cell therapy in Rockville, Maryland and Tarzana, California
  • Continuous manufacturing expansion in Mount Vernon, Indiana
  • Specialty manufacturing expansion in Coppell, Texas
  • New sites to supply clinical trials
  • Our growing research and development investment in novel medicines

Collectively, these investments will help deliver AstraZeneca’s ambition of reaching $80 billion in Total Revenue by 2030, of which we expect 50% would be generated in the US.

Howard Lutnick, US Secretary of Commerce, said: “For decades Americans have been reliant on foreign supply of key pharmaceutical products. President Trump and our nation’s new tariff policies are focused on ending this structural weakness. We are proud that AstraZeneca has made the decision to bring substantial pharmaceutical production to our shores. This historic investment is bringing tens of thousands of jobs to the US and will ensure medicine sold in our country is produced right here.”

Governor Glenn Youngkin, Commonwealth of Virginia, said: “I want to thank AstraZeneca for choosing Virginia as the cornerstone for this transformational investment in the United States. This project will set the standard for the latest technological advancements in pharmaceutical manufacturing, creating hundreds of highly skilled jobs and helping further strengthen the nation’s domestic supply chain. Advanced manufacturing is at the heart of Virginia’s dynamic economy, so I am thrilled that AstraZeneca, one of the world’s leading pharmaceutical companies, plans to make their largest global manufacturing investment here in the Commonwealth.”

Pascal Soriot, Chief Executive Officer, AstraZeneca, said: “Today’s announcement underpins our belief in America’s innovation in biopharmaceuticals and our commitment to the millions of patients who need our medicines in America and globally. It will also support our ambition to reach $80 billion in revenue by 2030. I look forward to partnering with Governor Youngkin and his team to work on our largest single manufacturing investment ever. It reflects the Commonwealth of Virginia’s desire to create highly skilled jobs in science and technology, and will strengthen the country’s domestic supply chain for medicines.”

Notes

AstraZeneca in the US
The US is AstraZeneca’s largest market and home to 19 R&D, manufacturing and commercial sites. We employ more than 18,000 people and support 92,000 jobs overall across the United States. In 2024 we contributed $5 billion directly to the economy and created approximately $20 billion worth of overall value for the American economy.

Today the US represents 42% of our Total Revenue with an ambition to reach 50% by 2030. This underscores the critical role the US plays in our ability to deliver on our ambition to launch 20 new medicines by the end of the decade.

AstraZeneca
AstraZeneca (LSE/STO/Nasdaq: AZN) is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines in Oncology, Rare Diseases, and BioPharmaceuticals, including Cardiovascular, Renal & Metabolism, and Respiratory & Immunology. Based in Cambridge, UK, AstraZeneca’s innovative medicines are sold in more than 125 countries and used by millions of patients worldwide. Please visit astrazeneca.com and follow the Company on social media @AstraZeneca

Contacts
For details on how to contact the Investor Relations Team, please click here. For Media contacts, click here.


Matthew Bowden
Company Secretary
AstraZeneca PLC

Phlow Announces Close of $37M Series C Financing to Accelerate Modern Medicine Development and Manufacturing in America

By News

Richmond, VA, July 22, 2025 (GLOBE NEWSWIRE) — Phlow Corp., a leading American pharmaceutical contract development and manufacturing organization (CDMO), today announced the successful close of its Series C financing round at an increased valuation from previous funding. The $37 million raise supports the Company’s mission of helping brilliant minds bring medicines to life through advanced development and manufacturing in America. The growing Company’s Series C round was led by Align Private Capital LLC, a woman-owned investment firm which manages private family office direct investment vehicles, and was supported by additional new and follow-on investors.

The funds raised will accelerate Phlow’s expansion across its U.S.-based development, manufacturing, and digital infrastructure, with a focus on scaling technology-driven innovation, including AI-powered systems and next-generation pharmaceutical manufacturing technologies. This growth will strengthen domestic production of Key Starting Materials (KSMs) and Active Pharmaceutical Ingredients (APIs), helping restore America’s pharmaceutical sovereignty. To date, Phlow has raised over $93 million in private capital, alongside more than $600 million in awarded government contracts.

“Raising funds in today’s capital market environment remains very challenging. This investment demonstrates the confidence that both new and existing investors have in our vision” said Dave Ryan, Chief Financial Officer of Phlow, “Together, with our bold and purpose-driven partners, these funds will permit us to continue to revolutionize the science behind life-changing medicines and improve the health of our nation, a focus over the last five years that has led to significant growth for our business and value creation for our investors. We are excited to work with the Align team to continue executing our vision.”

“We are excited to support the Phlow team as they address the inefficiencies and challenges in the current U.S. pharmaceutical supply chain. In particular, we applaud the Company’s initiatives to prevent pediatric drug shortages, to advance state-of-the-art tech-enabled API manufacturing, and to support the U.S. military,” said Anna Nekoranec, CEO of Align Private Capital.

Phlow’s Series C funding coincides with several significant milestones this year, including the two newly operational U.S.-based cGMP manufacturing facilities, capable of producing APIs at both kilogram and metric-ton scales using both batch and continuous processes. Additionally, Phlow recently partnered with the Joint Program Executive Office for Chemical, Biological, Radiological, and Nuclear Defense to develop medical countermeasure drug products that support the joint force and its allies in counteracting chemical and biological threats. At the same time, Phlow expanded its impact in the pediatric space, having shipped over 1.6 million vials of essential medicines to leading children’s hospitals across the country through the Children’s Hospital Coalition, a first-of-its-kind initiative to combat pediatric drug shortages.

“Phlow’s rapid growth and proven ability to achieve key milestones since our launch in 2020 are the result of bold leaders, visionaries, and partners working collaboratively to stabilize our supply chain and end chronic shortages of essential medicines and medical countermeasures for Americans,” said Eric S. Edwards, M.D., Ph.D., Chairman and CEO of Phlow. “The most recent funding round for Phlow validates our vital mission and accelerates our ability to support small molecule API development and manufacturing programs for small and large clinical and commercial volumes.”

In addition to its transformative partnerships with the U.S. Government, Phlow is rapidly expanding its next-generation CDMO services for pharmaceutical partners, providing advanced development and manufacturing solutions, such as continuous flow chemistry, that help drive cost competitiveness, minimize waste, and improve environmental outcomes, all while enabling accelerated speed-to-market.

About Phlow
Phlow, a B Corporation™, helps brilliant minds bring medicines to life through advanced development and manufacturing in America. Focused on innovations in drug substance development, Phlow supports government and private industry customers to create innovative approaches with scientific expertise, world-class manufacturing, and tech-enabled processes that propel the industry forward to a new standard as we create the future of how medicines are made. As a modern contract development and manufacturing provider, we measure our impact by increasing speed to market, reducing waste, and offering an environmentally friendly approach to manufacturing medicines that lead to healthy, resilient communities. For more, visit phlow-usa.com.

 

About Align Private Capital
Align Private Capital LLC, a woman-owned investment firm which manages private family office investment vehicles, was formed in 2014 to address the investment needs and challenges of Single-Family Offices. Align works with families on specific investment initiatives and more comprehensive portfolio analysis, investment planning, and implementation. The firm’s principals have extensive experience working with families in both alternative and traditional investment sectors. For more, visit alignprivatecapital.com.

CONTACT: Leslie Strickler Phlow Corp. leslies@etrecommunications.com Paul Spicer Phlow Corp pspicer@phlow-usa.com

TedcoZero

TEDCO Invests in Zero Point Five Therapeutics

By News

TedcoZeroCOLUMBIA, Md., (July 21, 2025) — TEDCO, Maryland’s economic engine for technology companies, announced a recent Venture Funds investment for nearly $350,00 in Zero Point Five Therapeutics. TEDCO’s evergreen Venture Funds are committed to investing in and advancing early-stage technology and life sciences companies across Maryland. These funds provide startups with access to a seasoned team dedicated to supporting their entrepreneurial growth and success.

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BioPharmaDive: Biotech startup funding dried up in second quarter, HSBC finds

By News

7/17/2025 –  – Even before HSBC’s report, there were signs of a biotech funding slowdown.

Research the investment bank Jefferies published in May and again in June found a substantial pullback in financing in public companies. Private rounds tracked by BioPharma Dive have gotten larger, but are fewer in number, too, as venture firms appear to be favoring surer bets. Initial public offerings have largely been on pause since the middle of February.

HSBC’s findings detail the fallout for drug startups more specifically. A combination of worries over pharmaceutical tariffs, research funding cuts and leadership changes at public health agencies drove a slump that led to startups’ worst quarter in terms of seed or Series A funding rounds since 2023, according to Jonathan Norris, a managing director at HSBC Innovation Banking.

The uncertainty has made investors more conservative, prompting them to shy away from smaller deals and band together for larger fundings, such as “megarounds” of $100 million or more. These investments allow companies to “get almost three traditional rounds” through one financing, Norris said.

Yet even megarounds dipped from 21 over the first three months to 16 between April and June. And along with that decline, the so-called crossover investors that often support the rounds preceding an IPO retreated from biotech venture deals. Only two of the top eight rounds included new crossover investors, a decline from each of the last two years.

“Many crossover investors are at their own proverbial crossroads, with too many private investments that have yet to IPO and many public companies struggling with low market caps,” Norris wrote in the report.

Their disappearance is, in part, due to the poor performance of companies that went public in 2024. The median stock price decline for last year’s class was 70% at the end of the first half, according to HSBC.

One bright spot is a steadier pace of M&A deals for private companies, which give venture capital firms another chance at investment returns. Last year, 17 drug startups were acquired — the highest total since 2020 — and buyouts are proceeding at a similar pace in 2025. Those deals prove “you can still get to an exit with early data in the right space,” Norris said.

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3 Days, 1 Region, Endless Opportunity: What to Expect at BHCR Week 2025

By News

3Days3EventsPlanning is well underway for BioHealth Capital Region Week 2025, and hundreds of attendees have already registered for the Forum taking place September 23–25 at US Pharmacopeia in Rockville, Maryland. Now in its 11th year, this free, three-day event brings together the people shaping the future of biohealth, including industry leaders, entrepreneurs, investors, government officials, and academic researchers, for insight, collaboration, and deal-making.

With this year’s theme, “Where Human and Artificial Intelligence Converge in the BioHealth Industry,” the program offers a timely look at how new technologies are transforming the entire innovation pipeline—from early-stage research through commercialization and patient impact.

The week opens with the BioHealth Capital Region Forum on September 23 and 24. This two-day event will feature keynote speakers, panels, and networking focused on industry trends, workforce strategies, and the impact of AI on research, development, and clinical decision-making. Whether you’re looking for policy updates, partnering opportunities, or inspiration, the Forum delivers valuable insight and access. Register today at https://bit.ly/BHCRWeek2025.

On September 24, the Crab Trap pitch competition returns for its 10th year, providing a platform for emerging companies to present their innovations to a panel of investors and strategic leaders. This year’s winner will receive a prize package, including a cash award (to be announced soon), $10,000 in CRO services from Noble Life Sciences and Accelevir, and a $25,000 IT and cybersecurity services credit from InfoPathways. Applications are open through August 29 at https://bit.ly/CrabTrap2025.

The week concludes with the BioHealth Capital Region Investment Conference on September 25. Designed to drive investor-startup engagement, the event features curated one-on-one meetings, startup quick-pitches, and opportunities to connect with some of the most promising companies in the region. It’s the best way to meet VCs, angels, and strategic partners seeking the next big thing in biohealth. Register at https://bit.ly/BHCRIC2025.

Thanks to the support of generous sponsors, all events are free to attend, but space is limited, and demand is growing. We are grateful to the organizations that have already committed to supporting this year’s programming and encourage others to consider joining them. Sponsorship includes visibility across all events and access to exclusive networking, including the VIP Leadership Dinner. For details, reach out to Rich Bendis at rbendis@biohealthinnovation.org or Andy Eckert at aeckert@biohealthinnovation.org.

Whether you’re an investor, entrepreneur, researcher, or policy leader, BioHealth Capital Region Week is your opportunity to engage with the people and ideas driving the future of healthcare innovation. We hope to see you there.

Jessica Nadler 200

Dr. Jessica Nadler

By Uncategorized

Managing Director- Deloitte Consulting, LLP
Jessica Nadler 200

Dr. Jessica Nadler focuses on transforming healthcare into a more human system. She focuses on data-informed strategy and policy, as well as their implementation, to improve outcomes for communities across the country. In her consulting career, Dr. Nadler has worked across translational medicine, patient centered care, public health grants portfolio strategy, and health information technology. As a geneticist, she served as an Assistant Professor at the University of North Carolina at Chapel Hill, where she focused on developing models of behaviors associated with autism. Dr. Nadler was also a Science & Technology Policy Fellow at the American Association for the Advancement of Science, within the Department of Health & Human Services.

blications in peer-reviewed journals, holds multiple patents, and has been invited to present at multiple international conferences. He holds a Ph.D. in Mathematics from Eberhard-Karls-Universität Tübingen (Germany), and a masters degree in mathematics and Physics from Eberhard-Karls-Universität Tübingen (Germany), as well as a Project Management Professional (PMP) certification.

 

 

i mab biopharma large

I-Mab Strengthens Givastomig Intellectual Property Portfolio through Acquisition of Bridge Health

By News

i mab biopharma largeROCKVILLE, Md., July 17, 2025 (GLOBE NEWSWIRE) — I-Mab (NASDAQ: IMAB) (the Company), a U.S.-based, global biotech company, focused on the development of precision immuno-oncology agents for the treatment of cancer, today announced that it entered into a definitive agreement to acquire 100% ownership of Bridge Health Biotech Co., Ltd. (Bridge Health). The transaction provides I-Mab with the rights to bispecific and multi-specific applications (including bispecific and multi-specific antibodies and antibody drug conjugates (ADCs)), based on the Claudin 18.2 (CLDN18.2) parental antibody used in the Company’s CLDN18.2 x 4-1BB bispecific antibody, givastomig.

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60degrees logo rgb logo

60 Degrees Pharmaceuticals Announces Pricing of Up to $10 Million Public Offering

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60degrees logo rgb logoWASHINGTON, July 15, 2025 (GLOBE NEWSWIRE) — 60 Degrees Pharmaceuticals, Inc. (the “Company” or “60 Degrees”) (Nasdaq: SXTP; SXTPW), a pharmaceutical company focused on developing new medicines for infectious diseases, today announced the pricing of a public offering of 2,631,578 shares of the Company’s common stock (or pre-funded warrants in lieu thereof) and accompanying Series A-1 warrants to purchase up to 2,631,578 shares of common stock and short-term Series A-2 warrants to purchase up to 2,631,578 shares of common stock, at a combined offering price of $1.90 per share of common stock (or per pre-funded warrant in lieu thereof) and accompanying warrants.

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Gain

Gain Therapeutics Announces Proposed Public Offering

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GainBETHESDA, Md., July 15, 2025 (GLOBE NEWSWIRE) — Gain Therapeutics, Inc. (Nasdaq: GANX) (“Gain”, or the “Company”), a clinical-stage biotechnology company leading the discovery and development of the next generation of allosteric small molecule therapies, today announced that it is proposing to offer and sell, subject to market conditions, shares of its common stock (or common stock equivalents in lieu thereof) and warrants to purchase common stock in an underwritten public offering. Gain expects to grant the underwriter a 30-day option to purchase up to an additional 15% of the shares of common stock and/or the warrants offered in the offering. All of the securities are being offered by the Company.

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CFF Logo 250

Cystic Fibrosis Foundation Commits Up to an Additional $24 Million for Prime Medicine to Develop Gene Editing Therapy

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CFF Logo 250BETHESDA, Md.–(BUSINESS WIRE)–Today, the Cystic Fibrosis Foundation announced an additional investment of up to $24 million in Prime Medicine to continue the development of a gene editing therapy for people with cystic fibrosis (CF).

Prime Medicine uses a gene editing technology called prime editing — a technology that enables a wide range of modifications to the DNA with a high degree of precision. The company — founded by Drs. David Liu and Andrew Anzalone, who pioneered the development of this unique editing technology — is investigating whether prime editing could treat several diseases, including CF.

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