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Case Study · Clin Pharm

Trial Design Optimisation

31%
COST SAVINGS
Up to 29%
SHORTER TRIAL DURATION
01

Challenge

Traditional clinical trials are costly, time-consuming, and inefficient, often requiring large participant numbers and extended durations. This delays critical decision-making and increases resource burdens.

02

Our Service

We offer Optimal Trial Design services to help you optimize clinical trials by maximizing data utility while reducing costs and timelines. Our approach combines Population PK Modeling, Variability Estimates, Significant Covariates, and Sparse Sampling Strategies to optimize outcomes and reduce the burden of data collection.

03

Outcome

Our optimized trial design delivers 31% cost savings and shortens trial durations by up to 29% while maintaining statistical power and data quality. This approach ensures faster, smarter, and more cost-effective clinical development.

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Summary

Cost Comparison

Traditional Design Cost: $8 million

Optimal Design Cost: $5.5 million (31% cost reduction due to fewer participants and shorter trial duration)

Trial duration

Traditional Design: duration of 28 days.

Optimal Design: duration of 20 days.

OPTIMAL TRIAL DESIGN SIGNIFICANTLY IMPROVES EFFICACY
REDUCES RESOURCE REQUIREMENTS AND ACCELERATES DRUG DEVELOPMENT
ENHANCES DECISION-MAKING PROCESS
POTENTIAL FOR WIDER APPLICATION IN CLINICAL TRIALS

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