Timing and amounts differ across media reports; these are not treated as audited figures.
Profile review: 2026-11-04 · Fields retain their individual source dates. Undisclosed values are not zero; early or historical events do not establish the latest financing. Awards and acquisitions are distinguished from equity rounds.
Disease tags match recorded text mentions and require program-level verification.
Technology, programs & evidence
The Degraducer website specifies bifunctional linkers and a ubiquitin–proteasome mechanism. Lead asset UBX-303-1 targets BTK.
An EMA public registry lists UBX-303-101 as Phase 1, with recruiting in Poland beginning in August 2026.
The website discloses a TPD R&D collaboration with SK Biopharmaceuticals.
Program / service
Target / indication
Representative stage
Evidence & scope
UBX-303-1
BTK · See individual trial / indication; not individually confirmed in this review
Phase 1
IND / clinical entry disclosed; public human results not confirmed in this review
Related news & literature
Company-name matches are discovery leads; verify entity identity and transaction roles in the original source.
No cataloged update explicitly mentions this company.
A Nature Materials study describes mRNA-loaded LNPs that reprogram tumor-associated macrophages into Claudin18.2-targeting CAR macrophages. The lipid formulation also promotes TREM2 internalization and degradation, reshaping immune responses. The original abstract reports tumor suppression and longer survival with PD-1 blockade in mice, plus ex vivo patient-sample findings. These findings do not demonstrate clinical efficacy in treated patients.
A Frontiers in Pharmacology review compares direct MCL-1 inhibition with approaches that reduce its abundance, including transcriptional interventions and targeted degradation. The original abstract highlights limited single-agent activity and cardiac safety concerns with inhibitors, while positioning degradation as an unvalidated clinical strategy. Biomarker-guided combinations and dynamic BH3 profiling are discussed; this review does not report a new clinical trial.
Evommune licensed EVO570, formerly HC118, from Hinova for development and commercialization outside Greater China. Upfront consideration totals $30 million: $20 million cash and $10 million in pre-funded warrants. Additional development, regulatory, and commercial milestones could reach approximately $1.1 billion, plus royalties. Phase 1 was expected to begin shortly; the announcement does not establish human efficacy.
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External reports state that the 2024 UBX-103 license to Yuhan ended in 2025; current rights require reconfirmation. A website licensing announcement incorrectly labeled UBX-303-1 as AR, and that error is not carried forward.
