Microbix’s Clot-Buster Drug Project Advances

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Microbix Biosystems Inc.
Microbix Biosystems Inc.

Sequel Pharma Executes Agreement with CDMO for Drug Product Manufacturing

MISSISSAUGA, Ontario, May 05, 2025 (GLOBE NEWSWIRE) -- Microbix Biosystems Inc. (TSX: MBX, OTCQX: MBXBF, Microbix®), a life sciences innovator, manufacturer, and exporter, announces that its funding and commercialization partner, Sequel Pharma, LLC (“Sequel”), has executed an agreement with a leading international contract development and manufacturing organization (“CDMO”) for production of the formulated and packaged drug (i.e.,Drug Product”) of Kinlytic® urokinase (“Kinlytic”), a biologic drug for dissolving blood clots.

Sequel is a U.S. based specialty pharma company with expertise in developing and commercializing niche drugs. It has committed to provide all funding needed to return Kinlytic to global markets, initially for the US$ 400 million U.S. market for dissolving clots in indwelling venous catheters (“Catheter Clearance”).

Kinlytic is an enzyme derived from human cell cultures that safely dissolves blood clots. Kinlytic is already approved for clinical use in the U.S. and the parties’ work is to validate new manufacturing for the drug and to re-enter the market by way of a supplemental biologics licensing application (“sBLA”).

The referenced CDMO agreement is for all actions necessary to resume production of Kinlytic Drug Product at a scale sufficient for the Catheter Clearance market. The CDMO has undertaken to complete this work over a timeframe specified by Sequel and in line with Microbix’s disclosed project objectives. The work of the CDMO will be overseen by Sequel, with scientific and technical assistance from Microbix.

It is Microbix’s intention to update its shareholders on further Kinlytic-related achievements as they become meaningful. Anticipated future disclosures related to Kinlytic may include, among other matters, successful new production of Drug Substance (active ingredient), first production of Drug Product, and clinical, regulatory, or commercial milestones. It is anticipated that Microbix will make one or more Kinlytic-related news release disclosures each year between now and the filing of a sBLA for the project, which is targeted to occur in calendar 2027.

Cameron Groome, CEO and President of Microbix, commented, “We’re very pleased that a detailed agreement has been executed with a very well-qualified CDMO for the production of new Kinlytic Drug Product. All parties will continue moving at full speed to revalidate and restart Drug Substance and Drug Product manufacturing using state-of-the-art methods and best practices.”