Back to dashboard
MedicaidPrior AuthMedium impact

Asparlas™ (calaspargase pegol-mknl) (Revised)

Humana·OH · Oncology, Pediatrics, Hematology·Medicaid
Effective date
Dec 1, 2025
We identified it
Aug 12, 2026
Days to comply

Summary

Humana Medicaid Ohio has issued a revised prior authorization policy for Asparlas (calaspargase pegol-mknl) effective December 1, 2025, with a revision date of July 22, 2026. Prior authorization is required for this drug with strict criteria: patient must have ALL diagnosis, be age ≤21 years, and use it as part of multi-agent chemotherapy. Five specific exclusion criteria may block approval, including prior serious thrombosis, pancreatitis, hemorrhage, disease progression on Asparlas, or elevated bilirubin levels.

Action Required

Action needed
By December 1, 2025: Billing team must implement prior authorization requirement for all Asparlas (calaspargase pegol-mknl) claims submitted to Humana Medicaid Ohio. Update billing system to flag claims for patients with ALL diagnosis requesting this drug for clinical review before processing. Providers must document: (1) ALL diagnosis confirmation, (2) patient age ≤21 years, (3) multi-agent chemotherapy regimen details, and (4) absence of exclusion criteria (prior thrombosis/pancreatitis/hemorrhage with asparaginase, disease progression on Asparlas, or total bilirubin >10x ULN). Add prior auth checklist to encounter forms or EMR template for oncology staff. Route all requests through Humana's preauthorization system (reference www.humana.com/PAL for coding details). Claims submitted without prior authorization approval will be denied. Initial approval duration is 6 months; renewal requests follow same criteria.
Asparlas™ (calaspargase pegol-mknl) (Revised) | Humana | PolicyChanges.app