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BCS

SEC Filing · DEF 14A

Silexion Therapeutics Corp

SLXNNASDAQEQUITYCurrent

SEC Filing

Filed Oct 5, 2026Accepted Oct 5, 2026, 4:09 PM EDTCIK 2022416Accession 0001178913-26-004708
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Company context

We are a clinical-stage biotechnology company developing, through our subsidiaries, RNA interference (RNAi) therapies for cancers driven by mutations in the Kirsten rat sarcoma viral oncogene homolog (“KRAS”). Our approach targets a significant unmet medical need, as treatment innovation for KRAS-driven cancers has historically lagged despite KRAS being one of the most common oncogenic drivers across solid tumors. In pancreatic cancer, for example, approximately 92% of patients have this mutated oncogene. While multiple pharmaceutical companies are pursuing strategies to inhibit KRAS and thereby limit its downstream signaling, our approach is differentiated by targeting the root cause of oncogenic signaling; our lead product candidate, SIL204, is a second-generation siRNA therapy that is engineered to suppress the KRAS oncogene itself, preventing the production of the oncogenic protein. We utilize an integrated treatment approach that combines administering SIL204 both directly into the tumor and systemically via subcutaneous injection, in combination with standard-of-care chemotherapy. In a previous Phase 2 clinical trial with our first-generation siRNA, the combination of siRNA and standard-of-care chemotherapy demonstrated an overall survival benefit compared to standard-of-care chemotherapy alone. Building on preclinical advancements and regimen optimization, we believe SIL204 has the potential to further improve clinical outcomes.

Current securities

Recent company filings

  1. Regulation FD DisclosureSep 30, 2026
  2. 424B3 filingSep 29, 2026
  3. Entry into a Material Definitive Agreement · Unregistered Sales of Equity Securities · Other EventsSep 29, 2026
  4. SCHEDULE 13D/A - filed by Moringa Sponsor, LP regarding Silexion Therapeutics CorpSep 28, 2026
  5. Regulation FD DisclosureSep 28, 2026

As-filed source

Primary evidence

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