InsightRX Apollo PK/PD Analytics for Clinical Trials

Drive Smarter Clinical Trials through Advanced PK/PD Visualization

InsightRX Apollo delivers advanced pharmacokinetic and pharmacodynamic analytics to empower biopharma teams with deep data insights, all supporting adaptive trial designs, patient subgroup analysis, and streamlined regulatory reporting.

InsightRX Apollo

Core features and capabilities

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Comprehensive PK/PD visualization

InsightRX Apollo provides robust tools to analyze and visualize PK/PD data across diverse patient populations. This enables biopharma teams to detect trends, identify outliers, and define therapeutic windows, supporting data-driven dosing decisions.

data-integration-services

Support for adaptive and precision dosing trials

The platform integrates seamlessly into clinical trial workflows to enable dynamic dose adjustments and adaptive study designs. This helps improve trial efficiency, patient safety, and regulatory confidence.

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Streamlined regulatory submission support

Generate detailed, audit-ready reports that comply with regulatory requirements. Apollo’s reporting capabilities facilitate smoother submissions, faster approvals, and maintain full data integrity throughout the trial lifecycle.

Additional Information

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Drive Success in Trials with Precision Dosing

Leverage InsightRX’s model-informed precision dosing platform to individualize dosing regimens, reduce variability, and improve safety and efficacy throughout your clinical development program.

Enhance Decisions with Companion Apps

Use InsightRX companion apps to deliver real-time, user-friendly dosing guidance. These tools integrate seamlessly with trial workflows to improve protocol adherence and support precise therapy management.

Security & Compliance for Clinical Research

InsightRX adheres to stringent data security and regulatory standards, including CE marking, ISO 13485, HITRUST certification, and GxP compliance, to support safe, reliable precision dosing throughout drug development and clinical trials.