What do you do when your PK/PD study demands impeccable timing, zero deviation, and novel biomarker development? For this double-dummy, placebo-controlled Phase 1 trial assessing two CNS-targeted drug formulations, a sponsor needed a partner who could manage over 4,620 tightly scheduled PK and PD sample times without missing a single one. They turned to Clinilabs. 

Get an inside look at how Clinilabs supported a high-complexity Phase 1I trial by: 

  • Initiating the trial in just 10 weeks  
  • Executing a 3:1 staff-to-subject ratio for precise sampling and safety 
  • Seamlessly coordinating QEEG, psychometric, and neuroendocrine assessments 
  • Delivering validated biomarkers to support further CNS drug development 

Ready to see what precision CNS trial execution really looks like? 

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When you need to get your product to the people who need it most, your pathway to CNS approval starts with Clinilabs.

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