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Pharming Group cuts 2026 revenue outlook, expects Joenja growth and RUCONEST stabilization
Pharming Group reported Q2 revenue of $90.2m, down 3% year‑over‑year, and lowered its 2026 revenue guidance to $375m–$395m while trimming operating expenses by $15m. RUCONEST sales fell 10% y/y to $72.3m but management expects patient metrics to support stabilization and a return to growth in H2 2026. Joenja revenue rose 40% to $17.9m, with U.S. pediatric dose filings and launches in Germany and Japan supporting an anticipated high‑30% annual growth for 2026. Two Phase II leniolisib readouts in broader primary immunodeficiency populations are expected in Q4, while cash and marketable securities stood at $159.5m at quarter end. » More on finance.yahoo.com
Pharming reports Q1 revenue decline despite strong Joenja growth
Pharming reported Q1 2026 revenue of USD 72.4 million (-8%) and a share-price plunge after the release. Joenja revenues rose 34% to USD 14.1 million but could not offset a 15% decline in RUCONEST to USD 58.4 million. Adjusted operating income worsened to a loss of USD 4.9 million, and cash and cash equivalents amounted to USD 171.8 million. Management confirmed the full-year guidance of USD 405–425 million and continues to pursue international expansion and indication expansion for Joenja. » More on de.investing.com
Pharming reaches operational profitability with 27% revenue increase
Pharming reports 2025 revenue of $376.1 million (+27%) and its first adjusted operating profit of $36.4 million. Drivers were RUCONEST ($317.9 million) and Joenja ($58.2 million); the quarter delivered $106.5 million in revenue and an adjusted operating profit of $6.5 million. The company expects 2026 revenue of $405–425 million with operating expenses of $330–335 million and cites near-term regulatory catalysts, in particular an FDA Type A meeting on pediatric approval of Joenja. Pharming is also expanding its pipeline (including Napazimon/KL1333) and plans clinical study advances and recruitment completions in the second half of 2026. » More on de.investing.com
Pharming Group reaches 52-week high after FDA approval of Leniolisib for children
Pharming Group’s stock rose to a 52-week high of 18.19 USD and is up 79.73% year-to-date and 70.66% over the past year. InvestingPro reports a gross profit margin of 89.9% and rates the company’s financial position as "GREAT." The FDA has approved the sNDA for Leniolisib to treat children aged 4 to 11 with APDS, extending the approval of the oral PI3Kδ inhibitor to a younger patient group. The combination of regulatory progress and strong share-price momentum underscores Pharming Group’s strengthened market position. » More on de.investing.com
Pharming Group reaches 52-week high after strong rally and FDA approval
Pharming Group’s stock climbed to a 52-week high of around $17.89–17.94 and has gained about 90.24% year-to-date (53.31% over six months). InvestingPro rates the financial situation as “GREAT,” highlighting a gross profit margin of 89.9% and revenue growth of 26.78%, but notes the stock may be trading above fair value. In addition, the FDA approved the supplemental application for leniolisib, making the treatment available for children aged 4 to 11 with APDS. » More on de.investing.com
Financials
| (EUR) | September 2026 | YoY |
|---|---|---|
| Revenue | 118.36m | 21.66% |
| Gross profit | 100.07m | 10.92% |
| Net profit | 22.55m | 198.69% |
| EBITDA | 30.67m | 30.91% |
Fundamentals
| Metric | Value |
|---|---|
Market capitalization | €779.62m |
Number of shares | 707.78m |
52-week high/low | €1.82 - €0.82 |
| Dividends | No |
Beta | 0.09 |
P/E ratio | 34.89 |
PEG ratio | 0.00 |
P/B ratio | 3.03 |
P/S ratio | 2.24 |
Company profile
Pharming Group N.V., a biopharmaceutical company, develops and commercialize protein replacement therapies and precision medicines for the treatment of rare diseases and unmet medical needs in the United States, Europe, and internationally. The company's lead product is Ruconest, a recombinant human C1 esterase inhibitor that is used for the treatment of acute hereditary angioedema. It also engages in the development of rhC1INH for the treatment of pre-eclampsia, acute kidney injury, and COVID-19; leniolisib, a phosphoinositide 3-kinase delta (PI3K delta) to treat patients with activated PI3K delta syndrome; and alpha-glucosidase therapy for the treatment of pompe and fabry diseases. The company has a development collaboration and license agreement with Novartis; and a strategic collaboration agreement with Orchard Therapeutics plc for research, development, manufacturing, and commercialization of OTL-105, an investigational ex-vivo autologous hematopoietic stem cell gene therapy for the treatment of hereditary angioedema. Pharming Group N.V. is headquartered in Leiden, the Netherlands.
| Name | Pharming Group |
| CEO | Kenneth Lynard |
| Headquarters | Leiden,
zh Netherlands |
| Website | |
| IPO | 16/06/1999 |
| Employees | 407 |
Ticker symbols
| Exchange | Symbol |
|---|---|
Euronext | PHARM.AS |
Pnk | PHGUF |
Amsterdam | PHARM.AS |
Frankfurt | PHGN.F |
DĂĽsseldorf | PHGN.DU |
London | 0QCO.L |
SIX | PHGN.SW |
MĂĽnchen | PHGN.MU |