Building The Future Of Early Detection & Regenerative Oncology
Prangenix develops multi-disease omics diagnostics and next-generation therapeutics targeting quiescent stem cells — starting with head and neck cancer.
- Detect
- Monitor
- Target


Oncology-Focused Diagnostics & Therapeutic Blueprinting for Personalized Care
Prangenix Therapeutics Pvt. Ltd. is a platform-first biotech company integrating multi-omics diagnostics and therapeutics targeting quiescent cancer stem cells (qCSCs), redefining the future of precision oncology. Headquartered in Eastern Uttar Pradesh, we specialize in liquid biopsy-based solutions for the early detection of head and neck cancers (HNSCC) using cfDNA, cfRNA, miRNA profiling, and AI-driven biomarker discovery. While our near-term focus is on advancing diagnostics, our long-term vision is a scalable, multi-disease platform enabling qCSC-targeted therapeutics through single-cell sequencing, CRISPR, and AI-powered drug discovery. Our mission is to deliver accessible, actionable, and affordable cancer care, empowering clinicians and patients to make earlier, faster, and better treatment decisions.
Two-Track Diagnostic Models

Track 1: Diagnostics (Dx) — Detect. Monitor.
Detect mutations, gene fusions, and epigenetic changes through circulating free DNA (cfDNA) and cfRNA, enabling early-stage detection and monitoring of treatment response without invasive biopsies.
Track 2: Therapeutics (Rx) — Target
Capture cancer stem cells from blood or tissue, apply single-cell sequencing, and create therapeutic blueprints for drug resistance, relapse prediction, and personalized treatment.
Our Expertise in Precision Care
We combine cutting-edge molecular diagnostics with non-invasive technologies to detect cancer signals even before symptoms appear.
Genomic Testing
through Liquid Biopsy
Prangenix performs non-invasive genomic testing using liquid biopsy to detect cancer-specific biomarkers, monitor disease progression, and enable early, accurate, and precision oncology diagnostics for improved patient outcomes.
Identify qCSCs
single cell omnics
Our platform identifies and profiles quiescent cancer stem cells (qCSCs) through single-cell sequencing, providing critical insights for targeted therapeutics and advancing personalized cancer treatment strategies.
Integrated platform
of single cell omnics
Prangenix’s integrated single-cell omics platform combines genomics, transcriptomics, and proteomics with AI-driven analytics to accelerate biomarker discovery, multi-omics diagnostics, and qCSC-targeted therapy development.
Next-Gen Cancer Diagnostics and Therapeutic Blueprinting
At Prangenix Therapeutics, we are building a next-gen platform for modular diagnostics, rare-cell profiling, and therapeutic blueprinting—designed to bring clarity, control, and customization to cancer and chronic disease care. Our goal is simple: make high-resolution molecular insight not only possible, but practical— for researchers, clinicians, and biotech innovators.
Modular Liquid & Tissue Diagnostics
Advanced liquid and tissue-based diagnostic platforms designed to detect early disease biomarkers with high accuracy and reliability.
Rare-Cell & qCSC Profiling
Profiling of rare cells and quiescent cancer stem cells (qCSCs) to understand resistance pathways and enable targeted therapeutic strategies.
Therapeutic Blueprinting
Personalized therapeutic blueprinting through CRISPR designs, CAR constructs, and precision solutions to transform cancer treatment outcomes.
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Disclaimer
The information provided on this website is intended for educational and informational purposes only. It should not be considered medical advice. Please consult your doctor or qualified health professional for guidance.