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*Correspondence: r.thompson@cam.ac.uk

MEYD‑773 displayed >250‑fold selectivity for class I PI3K over other kinases, with negligible activity against mTOR, DNA‑PK, and CDK families. In vitro, MEYD‑773 reduced p‑AKT (Ser473) and p‑S6 (Ser235/236) levels with EC₅₀ ≈ 30 nM, induced G₁ arrest, and triggered caspase‑3/7‑mediated apoptosis selectively in PI3K‑mutant TNBC cells (IC₅₀ = 0.08‑0.15 µM). PK studies revealed oral bioavailability of 68 %, a half‑life of 7.2 h, and plasma exposure exceeding the in‑vitro EC₅₀ for >12 h at 20 mg kg⁻¹. In orthotopic MDA‑MB‑231 models, daily oral dosing (20 mg kg⁻¹) produced a tumor growth inhibition (TGI) of 82 % (p < 0.001) without weight loss or histopathologic toxicity. In three independent TNBC PDX models (BRCA1‑mutated, PTEN‑null, and wild‑type PI3K), MEYD‑773 achieved TGIs of 71‑89 % and prolonged median survival by 3‑4‑fold compared with vehicle. Combination with standard‑of‑care paclitaxel showed synergistic tumor regression (Combination Index = 0.46). If you're ready to provide more context, I'll

The code "MEYD" follows the standard naming convention used by the Japanese adult video (JAV) industry. It is the series code for films released under the label, which is a subsidiary of the major production company MOODYZ .

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