Kanchan K Banerjee: Rusfertide Earns NCCN Category 1 Recommendation for Polycythemia Vera
Kanchan K Banerjee, Director of Strategy and Growth at WEbRx Lifesystems India Private Limited, shared a post on LinkedIn:
“Rusfertide Earns NCCN Category 1 in Polycythemia Vera: What the Update Signals
Takeda announced on September 21 that rusfertide (Mimrylo™), FDA-approved on August 28, 2026, has been included as a Category 1 option across both low- and high-risk PV in the NCCN Guidelines for Myeloproliferative Neoplasms. It is the only therapy carrying Category 1 status across both risk groups.
The eviden ce base (Phase 3 VERIFY, NCT05210790)
▪ Population: phlebotomy-dependent patients with uncontrolled hematocrit
▪ Clinical response (weeks 20-32): 76.9 percent with rusfertide + standard of care vs 32.9 percent with placebo + SOC (P < .0001)
▪ Key secondary endpoints, including phlebotomy burden, hematocrit <45 percent and fatigue, were met
▪ Most common adverse events: injection site reactions (47.4 percent) and anemia (25.6 percent)
Rusfertide sits alongside standard hematocrit-directed care, and treatment decisions remain with treating clinicians.
Strategic note: The view from the marketing desk
Guideline inclusion opens the door; it does not drive adoption on its own. Where to focus:
- Science first: lead with trial design, population and safety, including anemia.
- Precise patient definition: keep every asset anchored to the phlebotomy-dependent profile studied in VERIFY.
- Whole care team: phlebotomy nurses, clinic coordinators and pharmacists shape the pathway, so plan education for them alongside physician engagement.
- Access and patient support: with most spending out of pocket, in India, plan for affordability, access programs, patient education and counselling that supports injection technique and adherence
Swipe through the carousel for the clinical detail.
Views are my own. Please refer to the full prescribing information.”

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