Technology
How the OptimDosing Platform Works
OptimDosing combines individualized patient data with large-scale clinical evidence to recommend safe and effective medication doses and to monitor outcomes over time. The platform has two core pillars: the OptimDosing Engine for dose optimization and the RPM Platform for data integration and analytics.
Patented, evidence-fit dose optimization
The OptimDosing Engine fits each patient's profile to the most relevant clinical and real-world evidence to produce dosing recommendations for single- and multi-drug regimens. It accounts for interactions, cumulative toxicity, and therapeutic overlap, returning dose ranges with rationale and monitoring guidance.
Inputs
- Patient characteristics (age, comorbidities, phenotype)
- Medication list and dosing history
- Labs, device data, and clinical metrics
- Clinical trial, post-marketing, and registry evidence
Process
Criteria are derived from external evidence and fit to the individual's data. The engine then performs multi-drug dose optimization against safety and efficacy objectives.
Outputs
- Recommended dose per drug (with range)
- Supporting rationale and references
- Safety bounds and confidence indicators
- Suggested monitoring intervals
Pattern detection and real-world response insights
The RPM module ingests longitudinal lifestyle, medication, and symptom data to surface potential triggers and trend inflection points. Partners use it to visualize response, support adherence programs, and enable closed-loop dose refinement.
Data & Ingestion
- Wearables and connected devices
- Patient-reported outcomes and surveys
- EHR extracts and claims/registry data
- Nutrition, sleep, activity, and timing
Analytics
- Probable trigger and correlation detection
- Outcome trajectories and trend breaks
- Multi-factor views of dose–response
- Alerts and suggested follow-up monitoring
Integration Ready
Designed for seamless integration into existing healthcare workflows, EHR systems, and digital health platforms. API-first architecture enables rapid deployment.
Integration Options
SDK / API
Embed the engine and RPM endpoints into partner platforms. RESTful APIs with comprehensive documentation and developer support.
White-label Modules
Ready-made UI components for digital therapeutics. Customizable interfaces that maintain clinical accuracy and regulatory compliance.
Bespoke Studies
Custom analytics and integration for proprietary research. Tailored solutions for clinical trials, real-world evidence studies, and regulatory submissions.
Note: Technology is offered for licensing/acquisition. It is not cleared by the FDA for standalone clinical use.