Halozyme eyes continuous manufacturing platform in $2.1bn Evotec bid

The proposed acquisition of Evotec would essentially transform Halozyme from a therapeutics-based drug delivery platform into a full bioprocess services company.

Dan Stanton, Editorial director

November 22, 2024

3 Min Read
DepositPhotos/timbrk

Earlier this month, Halozyme Therapeutics made a bid to combine with Germany-based life science services firm Evotec for roughly €2 billion ($2.1 billion). The proposal would “diversify and extend Halozyme revenue and EBITDA growth and durability well into the next decade and beyond,” according to CEO Helen Torley, though it came as somewhat a surprise to Evotec.

“With respect to a media report, Evotec SE (“Company”) declares that it has received, without prior contact, a non-binding expression of interest from the listed US biotechnology company Halozyme Therapeutics Inc. regarding a takeover offer addressed to the shareholders of the Company with an offer price of €11.00 per share,” Evotec wrote in an ad hoc comment last week. “The Company will carefully analyze this expression of interest, decide on next steps, and inform the capital market in accordance with the legal requirements.”

But Halozyme has doubled down its desire to merge this week in an update that informed stakeholders as to how the addition of Evotec would “create a unique B2B global innovative pharma services company with complementary and leverageable platforms and cross-selling opportunities.”

Halozyme is a pioneer in the drug delivery space, with its Enhanze platform supporting numerous big pharma firms – including Roche, J&J, and Bristol Myers Squibb – in their development of subcutaneous biologics.

The technology consists of recombinant human hyaluronidase PH20 (rHuPH20), which helps overcome resistance to bulk fluid flow in the extracellular matrix, allowing high volumes of large molecules to be delivered under the skin. According to the firm, seven products incorporating the Enhanze platform have received approvals, including Roche’s Tecentriq SC (atezolizumab) and Herceptin SC (trastuzumab), argenx’ Vyvgart Hytrulo (efgartigimod alfa and hyaluronidase), and Takeda’s Hyqvia (Immune Globulin Infusion 10%).

Along with significant discovery and R&D assets, Evotec would bring Halozyme biologics contract development and manufacturing organization (CDMO) Just-Evotec.

The division, added for $90 million in May 2019, runs two facilities offering product and process development capabilities – including cell line development, up and downstream processing, and formulation development – in addition to early and late stage clinical supply and commercial manufacturing. The second “J.POD” facility opened in September in Toulouse, France, complementing the firm’s inaugural site in Redmond, Washington.

The facilities incorporate Just-Evotec’s continuous manufacturing platform. This includes the firm’s proprietary J.CHO cell line, a Chinese hamster ovary (CHO)-K1 host that is genetically engineered for glutamine synthetase (GS) knock-out, and a chemically defined media for perfusion culture of the line, allowing scalability in bioreactors of 3–1,000 L. Speaking at the BioProcess International Theater at BIO in June, Jon Gunther, vice president of business development, said the platform can reduce the cost of goods sold (COGS) by as much as 75%, using an example of a 15-day, 500-L perfusion culture producing a run yielding 5–8 kg of material.

The deal “comes as a surprise to many, since the deal would essentially transform the company from a therapeutics-based drug delivery platform into a healthcare services company,” Evercore ISI analyst Michael DiFiori wrote in a note.

“Bottom line: a lot still needs to happen in order for this deal to materialize and, assuming it does, Halozyme’s existing investor base would need to adapt accordingly.”

About the Author

Dan Stanton

Editorial director

Journalist covering the international biopharmaceutical manufacturing and processing industries.
Founder and editor of Bioprocess Insider, a daily news offshoot of publication Bioprocess International, with expertise in the pharmaceutical and healthcare sectors, in particular, the following niches: CROs, CDMOs, M&A, IPOs, biotech, bioprocessing methods and equipment, drug delivery, regulatory affairs and business development.

From London, UK originally but currently based in Montpellier, France through a round-a-bout adventure that has seen me live and work in Leeds (UK), London, New Zealand, and China.

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