Northwire Canada EditionSunday, July 12, 2026
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GLDN 0.055 +0.0% BRON 0.040 +0.0% BTO 5.43 −0.7% ESK 0.365 −2.7% AUMN 0.275 +0.0% GGX 0.040 +0.0% S 0.155 +29.2% NNX 0.035 +0.0% ABX 51.90 −0.6% TTS 2.40 −4.0% FCI 0.400 −9.1% GR 0.075 +0.0% AII 23.38 +12.4% TUNG 1.72 +1.8% LGO 1.01 −2.9% EMM 0.080 +0.0% GLDN 0.055 +0.0% BRON 0.040 +0.0% BTO 5.43 −0.7% ESK 0.365 −2.7% AUMN 0.275 +0.0% GGX 0.040 +0.0% S 0.155 +29.2% NNX 0.035 +0.0% ABX 51.90 −0.6% TTS 2.40 −4.0% FCI 0.400 −9.1% GR 0.075 +0.0% AII 23.38 +12.4% TUNG 1.72 +1.8% LGO 1.01 −2.9% EMM 0.080 +0.0%
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Rakovina Therapeutics to Present New Data at the AACR Annual Meeting 2026 - World's Premier Cancer Research Forum

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Executive Summary

  • Rakovina Therapeutics announced that two research abstracts will be presented at the 2026 AAC & R Annual Meeting in San Diego.
  • The first abstract details a novel brain‑penetrant dual ATR‑mTOR inhibitor designed with the Enki™ AI platform for PTEN‑deficient cancers.
  • The second abstract describes a lipid nanoparticle formulation of the bifunctional PARP/HDAC inhibitor Kt‑3283, created using the EnsaliX AI platform and NanoPalm collaboration.

Key Details

  • Abstract 1 – Dual ATR‑mTOR Inhibitor
  • Title: “A novel brain‑penetrant dual ATR‑mTOR inhibitor for PTEN‑deficient cancers.”
  • Session: DNA Damage and Repair 2 (Experimental and Molecular Therapeutics).
  • Date/Time: April 20, 2026, 9:00 AM – 12:00 PM; Abstract No. 5034.
  • Technology: Enki™ generative AI platform + Variational AI collaboration.
  • Target indication: PTEN‑deficient gliomas and breast cancers (up to 40% of gliomas, up to 63% of breast cancers).

  • Abstract 2 – Lipid Nanoparticle Formulation of Kt‑3283

  • Title: “Development of a lipid nanoparticle formulation of the bifunctional PARP and HDAC inhibitor kt‑3283.”
  • Session: Drug Delivery (Chemistry).
  • Date/Time: April 21, 2026, 2:00 PM – 5:00 PM; Abstract No. 4665.
  • Technology: EnsaliX AI platform + NanoPalm partnership (Riyadh, Saudi Arabia).
  • Goal: Improve encapsulation efficiency, cellular uptake, and pharmacological performance of Kt‑3283 for clinical translation.

  • Company Statements

  • CEO Kim Oishi highlighted the significance of presenting two abstracts for the second consecutive year and emphasized AI’s role in accelerating cancer drug development.
  • President & CSO Dr. Mads Daugaard noted the complementary nature of the two programs—enhanced delivery of an existing bifunctional compound and creation of new brain‑penetrant inhibitors.

  • Strategic Context

  • Rakovina’s preclinical pipeline targets DNA‑damage response vulnerabilities present in up to 75% of solid tumors, focusing on hard‑to‑treat cancers (breast, ovarian, prostate, brain).
  • Near‑term milestones include: in‑vivo testing of LNP formulations under the kt‑3000 program, progression of a lead candidate in the kt‑5000AI program, and initiation of pharmaceutical partnership discussions as data mature.

Notable Quotes

  • “We are thrilled that for the second year in a row, we are presenting two abstracts at the AACR Annual Meeting… We are using AI to solve problems that have held back cancer drug development for years.” – Kim Oishi, CEO
  • “What makes these two programs particularly exciting is that they address cancer from two distinct but complementary angles… one focused on smarter delivery of a proven bifunctional compound, and one on designing entirely new molecules to reach tumors that current therapies simply cannot access.” – Dr. Mads Daugaard, President & CSO
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