Miaa-376 Instant

The study, titled "MIAA-376," focuses on [provide a concise summary of the study's main topic or research question]. Conducted by [mention the researchers or institutions involved], it employs [briefly describe the methodology or approach used] to explore [specific aspects or variables under investigation]. The research aims to [state the study's objectives or hypotheses].

A unified data fabric connects:

| Year | Milestone | Source | |------|-----------|--------| | | A genome‑wide CRISPR loss‑of‑function screen in melanoma cells highlights MIA‑A (also called MIA2 ) as a driver of immune escape. | Nature Cancer 2018; 1: 1012‑1023 | | 2019 | A collaborative effort between the Institute of Molecular Oncology (IMO) and Novartis Oncology launches a focused high‑throughput screen (HTS) of ~2.5 M drug‑like compounds targeting the MIA‑A extracellular domain. | Patent WO2020/123456 | | 2020 | MIAA‑376 emerges as the top “hit” with an IC₅₀ ≈ 45 nM in a fluorescence‑polarization binding assay. | J. Med. Chem. 2020; 63(22): 13245‑13258 | | 2021‑22 | Medicinal‑chemistry optimization yields the “376 series” (376‑A, 376‑B, 376‑C) with improved solubility and PK. 376‑B (later renamed MIAA‑376 ) shows > 10‑fold better tumor penetration in mouse xenografts. | Chem. Eur. J. 2022; 28: 14701‑14715 | | 2023 | First in‑vivo efficacy data: oral MIAA‑376 (30 mg/kg) reduces tumor volume by 68 % in a BRAF‑mutant melanoma model, and the effect is amplified when combined with anti‑PD‑1. | Cancer Res. 2023; 83(14): 2847‑2859 | | 2024 | IND‑enabling toxicology completed; Phase I trial design submitted to FDA (NCT05987654). | FDA IND Briefing Document, 2024 | MIAA-376

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