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Pharming Group (PHAR)

Recent press releases and 8-K filings for PHAR.

Pharming Reports Strong Q3 2025 Results, Raises Guidance, and Details Growth Catalysts
PHAR
Guidance Update
Revenue Acceleration/Inflection
M&A
  • Pharming reported strong Q3 2025 results and raised its revenue guidance, driven by the continued growth of its two assets, RUCONEST and Joenja, which grew 29% in Q4 2024 year on year and 35%, respectively.
  • The company anticipates significant growth for Joenja, expecting FDA label expansion for the pediatric APDS population by end of January 2026, which could add 30% to its potential, and projects the reclassification of approximately 250 VUS patients over time, increasing APDS potential by 50%.
  • Pharming acquired Abliva, adding KL1333 for primary mitochondrial disease to its pipeline, an asset with more than a billion-dollar potential that is currently in registrational phase 2 trials and has undergone a positive futility analysis.
  • To optimize capital allocation and drive value, Pharming has cut 20% of its G&A headcounts and appointed Kenneth Lenertz as its new CFO.
Nov 19, 2025, 10:00 AM
Pharming Reports Strong Q3, Highlights Growth Drivers for RUCONEST and Joenja, and Discusses KL1333 Acquisition
PHAR
Guidance Update
Revenue Acceleration/Inflection
M&A
  • Pharming reported strong Q3 results and raised revenue guidance, driven by the continued double-digit growth of its two assets, RUCONEST and Joenja.
  • RUCONEST grew 29% in Q4 year-on-year, maintaining its position for severe HAE patients, while the company exited non-U.S. markets due to financial unsustainability.
  • Joenja grew 35% in Q4 year-on-year and is projected to become a billion-dollar drug, with significant growth opportunities including pediatric indication expansion (expected by end of January) and reclassification of 250 VUS patients.
  • Pharming acquired Abliva for KL1333, a drug for Primary Mitochondrial Disease (PMD) with billion-dollar potential currently in registrational Phase II trials, which has undergone a positive futility analysis.
  • The company is focused on optimal capital allocation, including a 20% cut in G&A headcounts, and recently attracted a new CFO, Kenneth Lynard.
Nov 19, 2025, 10:00 AM
Pharming Reports Strong Q3 Results, Raises Guidance, and Outlines Growth Strategies
PHAR
Guidance Update
Revenue Acceleration/Inflection
New Projects/Investments
  • Pharming reported strong third-quarter results and raised its revenue guidance, driven by RUCONEST growing 29% year-on-year in Q4 and Joenja growing 35%.
  • The company is focused on Joenja's high-growth potential, with expected FDA approval for pediatric expansion by the end of January, and the reclassification of VUS patients projected to increase APDS potential by 50%.
  • Pharming acquired KL1333 for primary mitochondrial disease, a registrational Phase 2 asset with billion-dollar potential that has undergone a positive futility analysis.
  • To optimize capital allocation, Pharming cut 20% of its G&A headcounts and appointed Kenneth Lenertz as the new CFO.
Nov 19, 2025, 10:00 AM
Pharming Group N.V. Reports Strong Q3 2025 Results and Raises Full-Year Revenue Guidance
PHAR
Earnings
Guidance Update
Product Launch
  • Pharming Group N.V. reported Q3 2025 total revenues of $97.3 million, a 30% increase year-over-year, with operating profit reaching $16.0 million.
  • The company raised its full-year 2025 total revenue guidance to $365-$375 million from the previous $335-$350 million, projecting 23%-26% growth.
  • Both commercial assets contributed significantly, with Ruconest revenue up 29% to $82 million and Joenja revenue increasing 35% to $15.1 million in Q3 2025.
  • The FDA granted priority review for Joenja's label expansion to 4- to 11-year-old children, with an approval date set for January 31, 2026, which is expected to be a significant growth driver.
  • Pharming is optimizing capital allocation through G&A headcount reductions and plans to complete the withdrawal of Ruconest from some European markets by the first half of 2026 due to financial sustainability.
Nov 6, 2025, 12:30 PM
Pharming Group N.V. Reports Strong Q3 2025 Financial Results and Raises Full-Year Revenue Guidance
PHAR
Earnings
Guidance Update
Revenue Acceleration/Inflection
  • Total revenues for Q3 2025 increased by 30% to US$97.3 million, with RUCONEST® revenue up 29% to US$82.2 million and Joenja® revenue up 35% to US$15.1 million compared to Q3 2024.
  • Operating profit for Q3 2025 surged by 285% to US$15.8 million, and the company generated US$32.0 million in cash flow from operations during the quarter.
  • Pharming raised its 2025 total revenue guidance to between US$365 million and US$375 million and received FDA priority review for leniolisib for children aged 4 to 11, with a decision expected by January 2026.
Nov 6, 2025, 11:04 AM
Pharming Group N.V. Implements Organizational Restructuring and Provides G&A Expense Reduction Update
PHAR
Layoffs
Guidance Update
  • Pharming Group N.V. announced the implementation of an organizational restructuring, which includes a 20% net reduction in non-commercial and non-medical headcount, primarily at its Netherlands headquarters.
  • The company remains on track to reduce total general and administrative (G&A) expenses by 15% or US$10 million annually.
  • Pharming anticipates recording approximately $7 million in one-time restructuring costs in the fourth quarter of 2025 related to the headcount reduction.
Oct 6, 2025, 3:45 PM
Pharming Group Announces FDA Acceptance and Priority Review for Leniolisib sNDA
PHAR
Product Launch
New Projects/Investments
  • Pharming Group N.V. announced the U.S. FDA's acceptance of its supplemental New Drug Application (sNDA) for leniolisib to treat children aged 4 to 11 years with Activated Phosphoinositide 3-Kinase Delta Syndrome (APDS).
  • The FDA granted Priority Review for the sNDA, with a Prescription Drug User Fee Act (PDUFA) target action date of January 31, 2026.
  • If approved, leniolisib would be the first and only treatment indicated for children aged 4 to 11 years with APDS, building on its existing U.S. FDA approval for patients 12 years of age and older.
Oct 1, 2025, 10:11 AM