Sapablursen for Erythrocytosis Control in Patients with Polycythemia Vera
Polycythemia vera is characterized by erythrocytosis and increased risk of thrombosis. Sapablursen is an antisense oligonucleotide that suppresses transmembrane serine protease 6 (TMPRSS6), increases hepcidin production, and reduces iron availability for erythropoiesis. IMPRSSION; an ongoing phase 2a, randomized, open-label study includes patients meeting 2016 WHO criteria for polycythemia vera, requiring ≥3 phlebotomies within 6 months of screening and ≥1 phlebotomy within the last 12 weeks. Cohort A (120 or 80 mg) and Cohort B (40 mg) received sapablursen subcutaneously once every 4 weeks (Q4W). The primary efficacy endpoint was the reduction in phlebotomy frequency from baseline to weeks 17-37 in patients who received ≥1 dose. Forty-nine patients received ≥1 sapablursen dose (median age 61 years; 82% male). The baseline mean±SD weekly phlebotomy rate was 0.15±0.07 in Cohort A; 0.17±0.07 in Cohort B and was reduced by -0.10 (95%CI, -0.13, -0.07; n=32;p<0.0001) in Cohort A; -0.10 (95%CI, -0.14, -0.06; n=17;p=0.0001) in Cohort B. Sapablursen reduced the median (IQR) number of phlebotomies from 5.0 (3.0-6.0,Cohort A; 3.5-6.5,Cohort B) at baseline (26-weeks) to 0 (0-1.0) in the efficacy evaluation window (20-weeks) in Cohort A and 1.5 (0-2.5) in Cohort B. Most adverse events were mild or moderate; anemia and fatigue were most common. The mean change in MPN-SAF-TSS at week 37 was -6.21 points (95%CI: -10.56, -1.85, p=0.0052) in Cohort A; -2.71 points in Cohort B (95% CI: -8.33, 2.91, p=0.34). Sapablursen reduced phlebotomy need, improved symptoms, and was safe and well-tolerated in patients with polycythemia vera. (Funded by Ionis Pharmaceuticals; ClinicalTrials.gov: NCT05143957)
Authors
- Prithviraj Bose (ORCID: https://orcid.org/0000-0002-4343-5712)
- Aaron T. Gerds (ORCID: https://orcid.org/0000-0002-3422-1309)
- Adam J. Mead (ORCID: https://orcid.org/0000-0001-8522-1002)
- Sanjay Bhanot (ORCID: https://orcid.org/0000-0002-9538-3491)
- Ross Baker (ORCID: https://orcid.org/0000-0002-2728-6788)
- Pankit J. Vachhani (ORCID: https://orcid.org/0000-0001-9779-6217)
- Ruben A. Mesa (ORCID: https://orcid.org/0000-0001-5880-7972)
- Keyvan Yousefi (ORCID: https://orcid.org/0000-0002-6115-1529)
- Caitlin O’Neill (ORCID: https://orcid.org/0000-0001-9227-5789)
- Jeanne Palmer (ORCID: https://orcid.org/0000-0002-2185-1504)
- Angela G. Fleischman (ORCID: https://orcid.org/0000-0002-3701-6079)
- Jon Ruckle
- Jonathan How
- Terrance D. Barrett (ORCID: https://orcid.org/0000-0002-0850-8365)
- Shiangtung Jung
- Ronald Hoffman
- Jonathan Sillar
Institutions
- University of Southern California (US)
- Atrium Health Wake Forest Baptist (US)
- Cleveland Clinic (US)
- Mayo Clinic (US)
- The University of Texas MD Anderson Cancer Center (US)
- University of California, Irvine (US)
- Ionis Pharmaceuticals (United States) (US)
- University of Alabama at Birmingham (US)
- Royal Victoria Hospital (CA)
- Mount Sinai Medical Center (US)
- MRC Weatherall Institute of Molecular Medicine (GB)
- MRC Human Immunology Unit (GB)
- Mayo Clinic in Arizona (US)
- Calvary Mater Newcastle Hospital (AU)
- Wake Forest Baptist Comprehensive Cancer Center
- Pacific Lutheran University (US)
Publication Details
- Journal
- Blood
- Published
- 2026-08-18
- DOI
- https://doi.org/10.1182/blood.2026033792
- Primary Topic
- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00