LymPro has completed two human clinical studies to date, and is set to move immediately into the Phase 2 validation study required to begin generating revenue as a laboratory developed test (“LDT”) at an already-selected Certified Laboratory Improvement Amendments (“CLIA”) certified laboratory. Thereafter, we anticipate LymPro will begin its regulatory process with the Food and Drug Administration towards approval.
Alzheimer's Diagnostic Market estimated at $500MM Annually. What if AMBS can build out just 20% of that market? Monster opportunity here potentially for investors!