
Chiesi–Aliada Partnership Advances BBB-Crossing Technology for Lysosomal Storage Disorders
Key Takeaways
- Chiesi Group's agreement with Aliada Therapeutics focuses on using BBB-crossing technology for lysosomal storage disorders, addressing unmet needs in CNS involvement.
- The MODEL platform offers advantages in CNS delivery and downstream functionality, potentially overcoming traditional ERT limitations due to BBB permeability.
The agreement centers on a worldwide, exclusive license to develop and commercialize enzyme replacement therapies using the proprietary platform technology.
Italy-based
The worldwide, exclusive license enables Chiesi Group to develop and commercialize enzyme replacement therapies (ERTs) using Aliada’s proprietary BBB technology (1). The agreement builds on a collaboration,
According to information provided by both companies at that time, the MODEL technology enables high therapeutic exposure in the brain, demonstrating advantages over competing approaches by offering a broad design landscape with an ability to optimize therapeutics for both central nervous system (CNS) delivery—many LSDs have CNS involvement—and downstream functionality (2).
How are company leaders welcoming the news?
“This agreement underscores our continued commitment to creating potential solutions that target the significant unmet needs in managing cognitive and neurological symptoms across several rare diseases,”
“We're proud to deepen our collaboration, propelling our partnership with Aliada to its next stage,”
What does this mean for the challenges of treating LSDs?
The partnership represents a strategic step toward overcoming one of the most persistent challenges in treating LSDs: effective delivery of ERTs across the BBB.
This collaboration underscores growing industry emphasis on molecular delivery technologies that bridge peripheral and CNS pathology. If successful, MODEL could provide a scalable approach to transporting biologics into the brain—an area where traditional ERTs have shown limited efficacy due to restricted BBB permeability (2).
From a manufacturing standpoint, Chiesi’s integration of this program into its Biotech Center of Excellence in Parma, Italy, may streamline the translation of these therapies from research to clinical-grade production (3). The partnership also illustrates a wider trend among mid-sized biopharma firms pursuing vertical integration—combining R&D, process development, and biologics manufacturing—to accelerate rare disease program timelines.
What else have these companies announced recently?
It has been nearly a year since AbbVie
In October 2024,
References
1. Chiesi Group.
2. Chiesi Global Rare Diseases.
3. Chiesi Group.
4. AbbVie.
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