Vanaja Konduri

Vice President, Research & Development Diakonos Oncology

Vanaja Konduri, PhD is an Assistant Professor in the Department of Pathology & Immunology at Baylor College of Medicine and serves as GMP Project Manager and acting VP of R&D for Diakonos Oncology leading Diakonos Oncology’s dendritic cell (DC)-based vaccine programs. Over 14 years in cell-based immunotherapy, she has translated bench discoveries into IND-enabled clinical trials, directing CMC strategy, technology transfer to GMP facilities, and assay validation across multiple Phase I/II programs spanning melanoma, dermal angiosarcoma, pancreatic ductal adenocarcinoma, and glioblastoma. Her foundational work defined how TH1-polarized DC vaccination combined with chemotherapy eradicates orthotopic pancreatic tumors and generates durable immune memory — research that seeded her current preclinical programs combining next-generation DC vaccines with targeted RAS inhibitors and CAR-T strategies. She holds patents in tumor mRNA amplification, multifactorial immune modulation, and DC-derived exosome characterization, and has led manufacturing readiness assessments and quality system integration for both clinical-trial and expanded-access vaccine products. Dr. Konduri also directs immunology coursework at Baylor College of Medicine and mentors trainees across the bench-to-bedside pipeline, bringing a dual perspective — rigorous immunologic science paired with hands-on GMP manufacturing leadership — to personalized cancer vaccine development.

Seminars

Tuesday 1st December 2026
Streamlining Manufacturing, Analytics & Supply Chain Operations to Accelerate Delivery of Personalized Cancer Vaccines
9:00 am

Reducing vein-to-vaccine timelines and achieving sustainable cost of goods requires more than operational optimization alone. This workshop will explore where speed and cost are truly won or lost across development, manufacturing, testing, and supply chain strategy, and what it takes to build commercially scalable personalized cancer vaccine programs.

Join this workshop to:

  • Identify which platform-level design choices (formulation complexity, cold-chain dependency, antigen design/selection speed) set the real ceiling on vein-to-vaccine timelines, independent of downstream process optimization
  • Explore how advances in antigen design and selection are compressing design-to batch-release timelines across different technology approaches
  • Optimize analytical and assay strategies to enable rapid batch release while maintaining product quality, safety, and regulatory compliance
  • Benchmark COGS drivers across personalized cancer vaccine technologies to identify where sustainable commercial economics are actually won or lost
Vanaja Konduri