
AstraZeneca: Externally Sponsored Scientific Research (ESR) – Oncology Focus
Independent investigators are invited to submit clinical and translational proposals on AstraZeneca oncology compounds, ranging from bispecific T-cell engagers and ATM inhibitors to antibody-drug conjugates and immune checkpoint modulators. Priority is given to studies that complement the core development programme and address unmet clinical needs.
Eligibility Criteria:
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Non-company researchers at academic medical centres or cancer institutes.
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Proposals must align with the specified areas of interest for each compound and not compete directly with ongoing registrational trials.
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Full compliance with GCP and local regulations is mandatory.
Funding Details:
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Support Type: Drug-only support, combination-strategy resources, biomarker assay kits, and translational-lab access.
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Key Compounds & Interests:
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AZD0486 (CD19×CD3 TCE): Combination and sequencing strategies in indolent NHL subtypes (WM/LPL, FL).
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AZD1390 (ATM inhibitor): Monotherapy or combination with radiotherapy for solid tumours.
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Calquence (acalabrutinib): RWE and mechanistic studies in CLL/SLL, MCL, iNHL, and DLBCL.
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Dato-DxD (datopotamab deruxtecan): AE-management and efficacy in NSCLC and breast-cancer populations, including resistance mechanisms and underrepresented cohorts.
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Enhertu (trastuzumab deruxtecan): Expansion into early-stage, HER2-low, and non-breast indications with real-world and mechanistic endpoints.
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Imfinzi (durvalumab): Biomarker-driven studies in NSCLC, SCLC, urothelial cancer, BTC, and HCC, plus novel screening approaches.
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Tagrisso (osimertinib): Resistance-overcoming strategies, biomarker-driven staging, and early-disease diagnostics.
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Truqap (capivasertib): AKT-pathway targeting and adherence studies in HR+ metastatic breast cancer.
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Deadline:
Continuous submission; decisions within 45 days of receipt.
Where to Go for Further Information:
Register at the AstraZeneca Open Innovation ESR portal. Reach out to the Oncology medical liaison for compound-specific guidance.
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