Pharming Group N.V. (PHAR) Form 6-K — Sep 22, 2026
Pharming announced positive Phase II topline data for leniolisib in genetically defined primary immunodeficiencies with immune dysregulation linked to PI3Kδ signaling, accepted as a late-breaking abstract at ESID 2026 (October 14-17, Netherlands). The single-arm, open-label, intra-patient dose-escalation study in 13 patients showed leniolisib was generally well-tolerated with clinical improvements in immune dysregulation, including a mean 26.4% spleen volume reduction and reduced index lesion size, with no new safety signals.
Key figures
- Cvid Subgroup
- 9
- Patients Enrolled
- 13
- Cvid Readout Timing
- Q4 2026
- Mean Spleen Volume Reduction
- 26.4%
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