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CD47-SIRPalpha Blockade Agent Safety Killing Methods Patent

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Summary

The European Patent Office published Sana Biotechnology Inc.'s patent application EP4225332A1 covering methods for triggering safety killing mechanisms using CD47-SIRPalpha blockade agents. The patent relates to cellular therapy applications including allogeneic cell transplants and engineered cell products. The application covers A61K and C07K classification technologies with designated states spanning 31 European countries.

What changed

EPO published European patent application EP4225332A1 for Sana Biotechnology Inc., titled 'METHODS FOR TRIGGERING SAFETY KILLING MECHANISMS USING A CD47-SIRP alpha BLOCKADE AGENT.' The application covers therapeutic methods utilizing CD47-SIRPalpha pathway blockade to trigger safety killing mechanisms in cell-based therapies, relevant to allogeneic cell transplants and engineered cellular products.

For biotechnology companies and pharmaceutical developers working on CD47-SIRPaxis targeting therapies or cell therapy products, this patent represents potential blocking intellectual property in European markets. Sana Biotechnology gains priority rights across 31 designated EPC contracting states. Competitors should assess this intellectual property when developing similar therapeutic approaches for commercialization in Europe.

What to do next

  1. Monitor patent prosecution timeline for EP4225332A1
  2. Review freedom-to-operate implications if developing CD47-SIRPalpha therapeutics in Europe

Archived snapshot

Apr 10, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← EPO Patent Bulletin

METHODS FOR TRIGGERING SAFETY KILLING MECHANISMS USING A CD47-SIRP alpha BLOCKADE AGENT

Publication EP4225332A1 Kind: A1 Apr 01, 2026

Applicants

Sana Biotechnology, Inc.

Inventors

SCHREPFER, Sonja

IPC Classifications

A61K 35/17 20150101AFI20250306BHEP C07K 14/725 20060101ALI20250306BHEP C12N 5/0783 20100101ALI20250306BHEP A61K 31/513 20060101ALI20250306BHEP A61K 31/522 20060101ALI20250306BHEP A61K 38/20 20060101ALI20250306BHEP A61K 39/395 20060101ALI20250306BHEP A61K 40/11 20250101ALI20250306BHEP A61K 40/15 20250101ALI20250306BHEP A61K 40/17 20250101ALI20250306BHEP A61K 40/24 20250101ALI20250306BHEP A61K 40/31 20250101ALI20250306BHEP A61K 40/42 20250101ALI20250306BHEP A61K 39/00 20060101ALI20250306BHEP C07K 14/705 20060101ALI20250306BHEP C07K 16/28 20060101ALI20250306BHEP C12N 15/86 20060101ALI20250306BHEP

Designated States

AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LI, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR

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Last updated

Classification

Agency
EPO
Published
April 1st, 2026
Instrument
Notice
Legal weight
Binding
Stage
Final
Change scope
Minor
Document ID
EP4225332A1

Who this affects

Applies to
Drug manufacturers Biotechnology companies Healthcare providers
Industry sector
3254.1 Biotechnology
Activity scope
Patent filing Cell therapy development Immunotherapy research
Geographic scope
European Union EU

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Healthcare Pharmaceuticals

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