News

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

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.

 

Read more here.

Recent News

05/22/2026

BIO Statement on Veto of Prescription Drug Affordability Boards (PDAB) in VirginiaPatrick J. Plues, Senior Vice President of State Government Affairs & Affiliate Relations at the Biotechnology Innovation Organization (BIO) released the following statement on the veto of Prescription Drug Affordability Boards (PDAB) legislation in Virginia: “BIO applauds Governor Spanberger’s decision to veto SB 271 and HB 483 — legislation that would have established a Prescription Drug Affordability Board (PDAB) and imposed arbitrary price controls in Virginia. The Governor’s action recognized an important point: even well-intentioned healthcare policies must be carefully designed to avoid unintended consequences for patients, providers, employers, and Virginia’s innovation economy. “BIO is proud to represent biotechnology companies developing the next generation of life-changing medicines, including many in the Commonwealth. We believe policymakers play a critically important role in helping advance both patient access to treatments and the continued growth of the life sciences sector. “We look forward to working with the Governor’s Administration, the General Assembly, Virginia Bio and other stakeholders to advance practical, patient-centered policy solutions that improve affordability while preserving access to care and the innovation ecosystem patients depend on.”

Patrick J. Plues, Senior Vice President of State Government Affairs & Affiliate Relations at the Biotechnology Innovation Organization (BIO) released the following statement on the veto of Prescription Drug Affordability Boards (PDAB) legislation in Virginia: “BIO applauds Governor Spanberger’s decision to veto SB 271 and HB 483 — legislation that would have established a Prescription

05/21/2026

Virginia Bio Applauds Governor Spanberger’s Veto of SB 271 and HB 483

The Virginia Biotechnology Association (Virginia Bio) today expressed strong support for Governor Abigail Spanberger’s decision to veto Senate Bill 271 and House Bill 483, legislation that would have established a Prescription Drug Affordability Advisory Panel (PDAAP) in the Commonwealth. Virginia Bio and the Virginia Chamber of Commerce sent a joint letter to Governor Spanberger commending

05/21/2026

New Global Clinical Society to Bring Focused Ultrasound Into Mainstream Medicine

The Focused Ultrasound Foundation today announced the launch of the International Focused Ultrasound Society (IFUS), a new organization dedicated to advancing clinical practice and accelerating adoption of focused ultrasound – a revolutionary, noninvasive therapeutic technology. Established as a program of the Focused Ultrasound Foundation, IFUS aggregates and expands the Foundation’s activities related to clinical implementation