Challenge:

A biotech designing a pivotal trial sought to reduce patient burden and improve recruitment while aligning with payer and market needs. 

What Efficus Health did:

Integrated patient insights, advocacy feedback, and cross-functional expertise (Medical Affairs, HEOR, Market Access) into protocol design. We ensured the study addressed both regulatory requirements and real-world evidence needs to support long-term adoption. 

Outcome:

Created a more patient-friendly, market-relevant trial that improved recruitment potential and generated data critical for adoption and reimbursement. The approach positioned the trial as both scientifically robust and commercially meaningful.