Pharming Group N.V.
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About the company
Pharming Group N. V. operates as a biopharmaceutical firm focused on creating and commercializing protein replacement therapies and precision medicines.
- CEO
- Fabrice Chouraqui
- IPO
- 2002
- Employees
- 407
- HQ
- Leiden, ZH, NL
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- Market Cap
- $782.10M
- P/E
- 64.42
- Fwd P/E
- 47.14
- PEG
- 0.00
- P/S
- 1.83
- P/B
- 2.61
- EV/EBITDA
- 17.89
- Div Yield
- 0.00%
- Gross Margin
- 86.50%
- Op Margin
- 4.00%
- Net Margin
- 2.57%
- ROE
- 3.52%
- ROIC
- 2.24%
Latest fiscal year · YoY change
- Revenue
- $391.32M+31.7%
- Gross Profit
- $343.99M+31.4%
- Op Income
- $20.09M
- Net Income
- $2.97M+125.0%
- EPS
- $0.00+124.3%
- OCF Growth
- +2993.7%
- FCF Growth
- +2074.6%
- 52W High
- $2.17
- 52W Low
- $1.10
- 50D MA
- $1.15
- 200D MA
- $1.43
- Beta
- 0.09
- RSI (14)
- 21
- Avg Volume
- 93
Earnings call summaries
Pick a quarter — each call distilled into takeaways, results, and a bull vs bear read.
Pharming posted Q2 revenue of $90.2 million, cut full-year revenue guidance by $30 million, but said RUCONEST is stabilizing and Joenja is still growing strongly.· July 30, 2026
- Q2 revenue was $90.2 million, down 3% year over year, with RUCONEST at $72.3 million and Joenja at $17.9 million.
- Management cut 2026 revenue guidance by $30 million to $375 million-$395 million, while reducing operating expense guidance by $15 million to $315 million-$320 million.
- RUCONEST demand indicators improved: active patients stayed at about 93% of prior-year levels, and new enrollments rose to 84 versus about 50 in Q1.
- Joenja grew 40% year over year, with U.S. revenue up 31% and international revenue up 150%; management highlighted Germany, Japan, and pediatric expansion as next drivers.
- Two Phase II studies in broader PID/CVID are fully enrolled, with top-line results expected in Q4 and a potential path to a larger registrational trial if positive.
Q2 2026 revenue was $90.2 million, down 3% year over year. RUCONEST revenue was $72.3 million, down 10% year over year and up 24% sequentially; Joenja revenue was $17.9 million, up 40% year over year. Reported operating profit was positive in the quarter; adjusted operating profit was also positive and down $5 million year over year. Operating cash flow was an outflow of $9.7 million, and cash and marketable securities were $159.5 million at quarter end. For H1 2026, revenue was $162.7 million, down 6%; adjusted operating profit was $10.7 million; and operating cash flow was an outflow of $7.7 million. Full-year 2026 revenue guidance was lowered to $375 million-$395 million, implying about 0%-5% growth versus 2025, and full-year operating expense guidance was cut to $315 million-$320 million, with gross margin expected to be around 89%. Kenneth said Joenja revenue is still expected to grow in the high 30%s for the full year, while RUCONEST U.S. revenue is expected to decline approximately 3% at the midpoint of guidance.
Fabrice Chouraqui framed the quarter as evidence that Pharming is becoming a more diversified rare disease company, with RUCONEST as a cash engine, Joenja as the growth asset, and pipeline programs as longer-term scale drivers. He acknowledged the revenue guide cut but stressed that the underlying business remains solid, citing RUCONEST patient resilience, improving enrollments, and strong Joenja momentum. His tone was constructive but disciplined, emphasizing tighter operating execution and multiple near-term catalysts.
Kenneth Lynard focused on profitability, cash, and cost control. He said Q2 operating profit was positive despite lower revenue and nearly $9 million of incremental investments versus last year, while adjusted operating profit was also positive; he also noted $6.5 million of non-recurring items in Q2, including $4.9 million of manufacturing inventory impairment and $1.7 million tied to the planned site closure in Évry, France. He highlighted $159.5 million of cash and marketable securities at quarter end, an outflow of $9.7 million in Q2 operating cash flow, and reaffirmed that existing cash plus future operating cash flow should fund the development pipeline and pre-launch activities. He also said full-year COGS should be about 11% of revenue, implying roughly 89% gross margin.
Analysts pressed on whether RUCONEST’s apparent enrollment recovery was sustainable, and management said Q2’s 84 new enrollments were close to Q2 2025 levels and that momentum has continued into July, though seasonality remains a factor. On Joenja, questions focused on Europe, pediatric uptake, and whether broader PID/CVID data could drive off-label sales; management said it does not expect to promote CVID data before FDA approval and does not expect CVID sales, but does expect APDS, pediatric, and geographic expansion to drive growth. Management also said the CVID and genetic PID studies are fully enrolled, top-line data are due in Q4, and if positive they would likely support a combined randomized Phase III trial in CVID.
The bullish read is that RUCONEST appears more resilient than feared after the oral competitor launch, with a stable active patient base and improving new enrollments and prescribers. Joenja is still compounding quickly, and management laid out several visible growth levers: Germany, Japan, U.S. pediatric expansion, and potential label expansion beyond APDS if the Q4 Phase II readouts are positive.
The main risk is that management still had to cut 2026 revenue guidance by $30 million, driven by RUCONEST market pressure and inventory normalization. RUCONEST revenue fell 10% year over year, and the company flagged a manufacturing inventory impairment plus a planned site closure-related charge. On Joenja, broader PID/CVID remains unproven, and management said they do not expect CVID sales until after a future registrational path and approval.
AI summary of the company's earnings call · Paraphrased · Not investment advice
- Free Float
- 99.3%
- Shares Outstanding
- 707.78M
- Float Shares
- 703.03M
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Generate PHGUF report →Pharming Group: Viable Contrarian Buy If Ruconest Stabilizes
seekingalpha.com · Sep 30
Pharming announces positive Phase II topline data for leniolisib in PIDs with immune dysregulation accepted as late-breaking abstract at ESID 2026
globenewswire.com · Sep 22
FDA approves Pharming's Joenja® as first treatment for children with APDS in the U.S.
globenewswire.com · Sep 11
Pharming Group to participate in Canaccord Genuity 46th Annual Growth Conference
globenewswire.com · Aug 4
Pharming announces U.S. FDA acceptance of sNDA resubmission for Joenja® (leniolisib) to treat children aged 4 to 11 years with APDS
globenewswire.com · Jun 4
Pharming Group announces results of 2026 Annual General Meeting of Shareholders
globenewswire.com · May 28
Pharming Group N.V. (PHAR) Q1 2026 Earnings Call Transcript
seekingalpha.com · May 7
Pharming Group announces presentations at CIS 2026 Annual Meeting, including leniolisib pediatric data in APDS and clinical experience in CVID and related disorders
globenewswire.com · May 7
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