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eXoZymes Selects Curia as Commercial-Scale Manufacturing Partner for NCT

eXoZymes partners with CDMO Curia to transfer and scale its NCT process from pilot validation toward planned commercial-scale manufacturing.

(Moderate)
(Very Positive)
Tags
partnership

eXoZymes (EXOZ) has entered a commercial-scale manufacturing agreement with Curia Global to advance production of its NCT product, with program activities expected to begin in the fourth quarter of 2026.

Under the agreement, eXoZymes will transfer its proprietary NCT manufacturing process to Curia, which will scale it at facilities in León, Spain, and Rozzano, Italy. The work covers cross validation of enzyme fermentation, cell-free reaction and purification steps, alongside process modeling and engineering analysis, to define a technical roadmap for larger-scale and potential commercial manufacturing of NCT in 2027.

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Positive

  • Commercial-scale partnership signed with Curia to transfer and scale NCT manufacturing
  • Program start targeted Q4 2026 with roadmap to larger-scale production in 2027
  • Multi-site manufacturing capability at Curia’s León and Rozzano facilities for NCT scale-up

Negative

  • None.

Market Context

The Aug 18 NCT process update was followed by a 0.16% 24-hour gain; this agreement moved the same pr...
Analysis

The Aug 18 NCT process update was followed by a 0.16% 24-hour gain; this agreement moved the same program from pilot-scale validation into Curia technology transfer for larger-scale manufacturing.

Key Figures

Program commencement: Q4 2026 Larger-scale production roadmap: 2027
Program commencement
Q4 2026
Curia commercial-scale manufacturing program
Larger-scale production roadmap
2027
Planned subsequent production scale-up

Historical Context

2 past events · Latest: Aug 18
2 events
  1. Aug 18

    NCT process update

    24h Move
    +0.2%

    Optimized NCT process increased productivity tenfold and reduced reaction time by over 80%

  2. Aug 20

    Q2 earnings update

    24h Move
    +1.6%

    Reported NCT manufacturing progress alongside Q2 results and planned commercial development

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Key Terms

technology transfer, cell-free reaction, cell-free biomanufacturing, cdmo, +1 more
5 terms
technology transfer technical
"Our facilities in León and Rozzano offer deep expertise in technology transfer"
Technology transfer is the process of moving an invention, know‑how, or technical capability from one organization to another so it can be developed, manufactured or sold. For investors it matters because successful transfers turn research or prototypes into marketable products or revenue streams—similar to handing a recipe and kitchen to someone who can scale it up—and they affect a company’s growth prospects, costs, timelines and competitive position.
cell-free reaction technical
"from enzyme production through the cell-free NCT reaction to product purification"
A cell-free reaction is a biochemical process run outside living cells using cell extracts or purified enzymes and molecular components to copy DNA/RNA, make proteins, or carry out metabolic steps. It matters to investors because companies use cell-free systems to develop medicines, diagnostics, and biologic manufacturing more quickly and with simpler safety and scale needs—like testing recipes on a countertop instead of operating a full restaurant kitchen.
cell-free biomanufacturing technical
"The company's platform is designed to replace inefficient extraction"
Cell-free biomanufacturing makes biological products — like proteins, enzymes or vaccine ingredients — by using the molecular machinery of cells removed from living organisms, rather than growing whole cells. Investors should care because this approach can speed up production, cut costs and reduce contamination risk, making supply chains more flexible and potentially changing how quickly and cheaply biotech products reach the market.
cdmo technical
"Curia is a contract research, development and manufacturing organization (CDMO)"
A contract development and manufacturing organization (CDMO) is a company that provides specialized services to help develop and produce pharmaceutical products for other businesses. Think of it as a contract factory that takes a company's recipe and makes the product on their behalf. For investors, CDMOs are important because they support the growth of pharmaceutical companies and can be key partners in bringing new medicines to market.
sterile fill-finish manufacturing technical
"regulatory support, analytical services, drug substance and sterile fill-finish manufacturing"
Sterile fill-finish manufacturing is the controlled process of putting a finished sterile drug or vaccine into its final containers (vials, syringes, cartridges) and sealing and labeling them under strict clean-room conditions to prevent contamination. It matters to investors because this step determines whether a product meets regulatory quality standards, affects production speed and supply reliability, and can be a bottleneck or competitive advantage much like a bottling line determines how quickly and safely a beverage reaches store shelves.

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  • Program expected to commence in Q4 2026 and establish a roadmap for larger-scale production in 2027

LOS ANGELES, CA / ACCESS Newswire / September 8, 2026 / Today, eXoZymes Inc. (NASDAQ:EXOZ) ("eXoZymes") - a pioneer of AI-enhanced enzymes that transform abundant feedstock into valuable nutraceuticals and novel medicines - announced that it has entered into an agreement with Curia Global, Inc. ("Curia"), a global leader in contract manufacturing, to initiate technology

The agreement represents the next major step in advancing eXoZymes' proprietary NCT manufacturing process from successful pilot-scale validation toward commercial manufacturing.

Damien Perriman, Chief Commercial Officer of eXoZymes, states, "We are advancing the work required to establish the manufacturing pathway and supply chain to support NCT's planned commercial launch. The Curia engagement establishes the manufacturing foundation required to support commercial customer qualification, future supply agreements, and the planned market introduction of NCT."

Under the program, eXoZymes will transfer its NCT manufacturing process to Curia who will scale the process at its facilities in León, Spain, and Rozzano, Italy. The work includes cross validation of eXoZymes' proprietary, enzyme fermentation, cell-free reaction, and purification processes to support larger-scale and eventual commercial manufacturing. The program also includes process modeling and engineering analysis to define a recommended path to larger-scale manufacturing, further de-risking eXoZymes' route to commercial NCT supply.

Jamie Grabowski, President of R&D at Curia, adds, "Curia is proud to partner with eXoZymes as they advance NCT toward commercialization. Our facilities in León and Rozzano offer deep expertise in technology transfer, process development, and manufacturing, and they are well positioned to support this innovative program and help establish a reliable route to larger-scale NCT production."

Paul Opgenorth, PhD, VP of Development and co-founder of eXoZymes, elaborates, "We have demonstrated the NCT process at pilot scale and substantially improved its productivity and economics. Transferring our entire integrated process - from enzyme production through the cell-free NCT reaction to product purification - into a commercial manufacturing environment represents an important validation of its maturity. Having visited Curia's facilities in both Spain and Italy, I'm confident we have selected a partner with the technical capabilities and infrastructure to take this next step with us."

The program is expected to progress during the fourth quarter of 2026 and is designed to establish the technical roadmap for subsequent larger-scale production in 2027.

About Curia Global
Curia is a contract research, development and manufacturing organization (CDMO) with an integrated network of 20+ global sites and 3,000+ employees supporting biopharmaceutical customers from discovery through commercialization. Our capabilities span small molecules, generic APIs and biologics, with expertise in regulatory support, analytical services, drug substance and sterile fill-finish manufacturing. Founded in 1991 as Albany Molecular Research, Inc. (AMRI), Curia built its foundation on scientific innovation and was originally known for the discovery and development of the active pharmaceutical ingredient in Allegra. Over the last three decades, Curia has expanded its capabilities and global footprint through strategic acquisitions, including Crystal Pharma, Euticals, Gadea Pharmaceutical Group, Integrity Bio, LakePharma and Ragactives. Today, Curia partners with customers to accelerate discovery, development and manufacturing timelines to help bring life-changing therapies to patients. Visit Curia at curiaglobal.com

About eXoZymes
Founded in 2019, eXoZymes is pioneering a cell-free biomanufacturing platform that uses AI-enhanced enzymes - called exozymes - to make valuable natural products and new analogs outside living cells. The company's platform is designed to replace inefficient extraction and petrochemical processes with a scalable way to produce high-value molecules for nutraceutical and pharmaceutical markets.

eXoZymes is building a portfolio of biosolutions across NCT, cannabinoid analogs, santalene, and other high-value natural product molecules, with potential commercialization paths that include partnerships, licensing and joint ventures. Learn more at exozymes.com

eXoZymes Safe Harbor
This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements, which are based on certain assumptions and describe the company's future plans, strategies and expectations, can generally be identified by the use of forward-looking terms such as "believe," "expect," "may," "will," "should," "would," "could," "seek," "intend," "plan," "goal," "project," "estimate," "anticipate," "strategy," "future," "likely," "potential," or other comparable terms, although not all forward-looking statements contain these identifying words. All statements other than statements of historical facts included in this press release regarding the company's strategies, prospects, financial condition, operations, costs, plans and objectives are forward-looking statements. Actual results could differ materially for a variety of reasons. You should carefully consider the risks and uncertainties described in the "Risk Factors" section of eXoZymes' quarterly reports on Form 10-Q, annual reports on Form 10-K, and other documents filed by eXoZymes from time to time by the company with the Securities and Exchange Commission. These filings identify and address important risks and uncertainties that could cause actual events and results to differ materially from those contained in the forward-looking statements. Forward-looking statements speak only as of the date they are made. Readers are cautioned not to put undue reliance on forward-looking statements, and eXoZymes assumes no obligation and does not intend to update or revise these forward-looking statements, whether as a result of new information, future events, or otherwise. eXoZymes does not give any assurance that it will achieve its expectations.

eXoZymes contact
Lasse Görlitz, VP of Comms & IR
(858) 319-7135
press@exozymes.com

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SOURCE: eXoZymes



View the original press release on ACCESS Newswire

FAQ

What specific work will Curia perform for eXoZymes under the NCT program?

Curia will receive a transfer of eXoZymes’ NCT manufacturing process and scale it at its León and Rozzano sites. The program includes cross validation of enzyme fermentation, cell-free reaction and purification processes, plus process modeling and engineering analysis to define a recommended path to larger-scale and eventual commercial manufacturing of NCT.

What timeline does eXoZymes outline for NCT scale-up and commercialization steps?

The program with Curia is expected to progress during the fourth quarter of 2026 and is designed to establish the technical roadmap for subsequent larger-scale NCT production in 2027, supporting planned commercial customer qualification, future supply agreements and a potential market introduction of NCT.

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