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Paz Vellanki, MD, PhD
Former FDA oncology leader recognized for translating complex regulatory insight into actionable development strategy. Served as Associate Director in the FDA’s Division of Oncology 2, where she helped shape regulatory decisions and guide drug development across lung cancer, head and neck cancer, and rare tumors. Combines deep expertise in clinical trial design, INDs and drug applications with leadership in advancing novel endpoints, including serving as technical lead on FDA guidance for circulating tumor DNA (ctDNA) in early-stage solid tumors.
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Read: The Operational Reality of Clinical Trial Technology
The Operational Reality of Clinical Trial Technology
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Read: Case Study: FIH Radiopharmaceutical Trial Across South Korea and US
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Read: Case Study: Global Phase 2 Drug Delivery in Advanced Colorectal Cancer
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Read: Case Study: Managing Complexity in an Autologous Cell Therapy Trial
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Read: How Investigator Engagement Builds Enrollment Momentum
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Read: Case Study: Nectin 4 Biomarker Testing for Oncology Clinical Programs
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Read: Has the rest of the world finally caught up with Latin America?
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Read: Case Study: Rapid Execution of Assay Validation Rescued Global Study
DiscoverTranslational Research - Assays
Case Study: Rapid Execution of Assay Validation Rescued Global Study
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Read: Clinical AI at Scale: Why Trust Matters More Than Speed
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