Praedicare's revolutionary SoS approach accelerates drug development. With first-of-its kind integrated multiple wet lab systems, system of mathematical models, suite of AI tools, and clinical trial databases to give outcomes that are emergent properties that reduce timelines 2-3 times, >90% of costs, and maximize phase-by-phase success rates from preclinical phases to NDA/BLA.
Reduce Drug Development costs by up to up to 90%
Accelerate drug development cycle from bench to clinic by 2-3x
De-risk patient's lives by reducing death and adverse events by 50%
We are dedicated to transforming healthcare through our innovative solutions. By reducing drug development costs by up to 20x, accelerating the development cycle by 2-3x, and significantly improving patient safety, Praedicare is revolutionizing the healthcare landscape. Explore our cutting-edge technologies and discover how we are reshaping the future of healthcare, one advancement at a time.
Rates of Response in Patients
How Many Patients Will Respond
Optimal Duration of Therapy
Doses to Minimize Failure & Resistance
Personalized Therapy
Modeling Solutions
Will drug be efficacious in humans? If so, at what dose? -Are there potential toxicity risks that can be identified early? If so, at what dose?
Are there potential opportunities to improve efficacy through drug combinations? If so, what drug(s) and doses?
How best to align our regulatory strategy, pre- clinical and clinical plans to mitigate risk?
Demonstration of commercial viability of drug to investors & partners
Accurately predict efficacy and toxicity signals during preclinical phase
Optimal drug doses for combinations using factorial design
Reduce drug development timelines using our quantitative forecasting
Data and models that we have generated has been used by clients throughout the regulatory process by international regulatory bodies
We can help clients identify potential collaborators and investors
Rates of Response in Patients
How Many Patients Will Respond
Optimal Duration of Therapy
Doses to Minimize Failure & Resistance
Personalized Therapy
Modeling Solutions
Will drug be efficacious in humans? If so, at what dose? -Are there potential toxicity risks that can be identified early? If so, at what dose?
Are there potential opportunities to improve efficacy through drug combinations? If so, what drug(s) and doses?
How best to align our regulatory strategy, pre- clinical and clinical plans to mitigate risk?
Demonstration of commercial viability of drug to investors & partners
Accurately predict efficacy and toxicity signals during preclinical phase
Optimal drug doses for combinations using factorial design
Reduce drug development timelines using our quantitative forecasting
Data and models that we have generated has been used by clients throughout the regulatory process by international regulatory bodies
We can help clients identify potential collaborators and investors
predict performance in
clinical trials for clinical trial design and adaptive clinical trial design.
research in North America and 28 African countries. Modeling to support clinical trials and dose selections.
Clinical Forecasting
predict performance in
clinical trials for clinical trial design and adaptive clinical trial design.
Research
research in North America and 28 African countries. Modeling to support clinical trials and dose selections.
Model Uses Include:
Optimized clinical trial design, including sample size and adaptive designs
Identify and develop biomarkers to optimize clinical trial design and provide biology-driven clinical trial therapeutic endpoints
Custom-made hollow fiber technology and 3D human organoids combined with advanced ‘omics, bulk and single cell sequencing for drug discovery, biomarkers, IP strengthening/submission, safety, and IND submissions.
& Clinical Trials
Model Uses Include:
Optimized clinical trial design, including sample size and adaptive designs
Identify and develop biomarkers to optimize clinical trial design and provide biology-driven clinical trial therapeutic endpoints
Custom-made hollow fiber technology and 3D human organoids combined with advanced ‘omics, bulk and single cell sequencing for drug discovery, biomarkers, IP strengthening/submission, safety, and IND submissions.
Number of Biopharma
Companies Worked With
Number of Projects
Worked On
Number of Biopharma
Companies Worked With
Number of Projects
Worked On