Be the scientist who finds the breakthrough with Zeta. Discover combination therapies, design trials, create drugs, and validate hypotheses... in minutes, not months.
Individually rare, collectively burdensome, economically neglected. Critical insights scattered across fragmented data sources with no centralized infrastructure to connect them.
An agentic intelligence layer integrating curated rare cancer databases, clinical trial registries, research literature, and bioinformatics tools. Recursive reasoning loops traverse unified biomedical ontologies, transforming fragmented knowledge into connected therapeutic insights.
Built for researchers advancing therapies where traditional pharmaceutical economics fail patients.
Four specialized databases, unified into a single ontology connecting genes, drugs, trials, and phenotypes
Curated database linking rare cancer types to therapeutic compounds, biomarkers, and clinical research
Comprehensive cancer drug database with FDA approval status, clinical trial data, and molecular targets
Self-hosted index of all registered clinical studies from ClinicalTrials.gov via AACT
Comprehensive document library with research papers, clinical guidelines, and treatment protocols
Live access to authoritative medical databases and regulatory sources
Real-time literature search across PubMed and PubMed Central
European rare disease database with expert-curated information
Standardized cancer terminology ontology from the National Cancer Institute
Live access to drug labels, adverse events, and drug interactions
Disease-symptom relationships and phenotypic abnormalities
Cross-database entity linking and standardized vocabularies
Calculate physicochemical properties including molecular weight, logP, TPSA, and drug-likeness
Validate chemical structures and generate molecular diagrams from SMILES strings
Query molecular information, bioactivity data, and compound properties
All data enriched and validated against authoritative medical sources
Recursive agents and machine learning models transform data into breakthrough insights
Advanced AI reasoning model that thinks through complex chemistry problems step-by-step. ETHER0 explores drug design opportunities by generating hypotheses, evaluating molecular structures, and proposing novel therapeutic candidates. It identifies promising scaffolds and optimizes drug-like properties for rare cancer targets.
Read about ETHER0
Industry-leading 16-model ML ensemble predicting blood-brain barrier permeability. Trained on 7,000+ compounds for targeted therapy development in CNS rare cancers. Identifies which treatments can effectively reach brain tumors and neurological targets.
Visit PredictBBB.aiYour co-scientist for discovering novel therapies and unlocking clinical trials for rare cancers. Zeta investigates autonomously across multiple rounds of inquiry, deciding when to dive deeper and when to synthesize findings.
Search PubMed for rare cancer papers, sift through abstracts one by one, no connections between entities
3-4 hoursNavigate ClinicalTrials.gov filters, decode eligibility criteria, manually match patient biomarkers
2-3 hoursCross-reference FDA labels, ORPHANET disease data, and molecular databases separately
2-3 hoursCompile fragmented findings from disparate sources, manually identify therapeutic opportunities
2-4 hoursManual, fragmented, time-intensive
Ask your research question in plain English about rare cancer therapies, biomarkers, or trials
InstantZeta simultaneously queries rare cancer databases, clinical trials, literature, and drug data
SecondsAI analyzes initial findings, decides which leads warrant deeper investigation, executes follow-up searches
MinutesCitation-backed analysis with drug candidates, trial matches, biomarker correlations, and knowledge graphs
CompleteAutonomous, integrated, accelerated
From question to insight in minutes. Watch how Zeta transforms rare cancer research with autonomous intelligence.
Stop wasting weeks searching through fragmented databases and disconnected literature. Zeta's recursive AI agents work 24/7 to synthesize evidence, identify novel drug combinations, and surface breakthrough insights you'd never find manually.