Pharming Group (PHG) Q3 2026 Earnings Report
DE:PHG Q3 2026 EPS Results
- Actual EPS
- EUR 0.27
- Consensus EPS
- EUR 0.19
- Beat/Miss
- Beat by +EUR 0.08
- One Year Ago EPS
- EUR 0.09
DE:PHG Q3 2026 Revenue Results
- Actual Revenue
- EUR 104.89M
- Expected Revenue
- EUR 105.00M
- Beat/Miss
- Missed by -EUR 108.54K
- YoY Revenue Growth
- +21.29%
Earnings Announcement Details
- Quarter
- Q3 2026
- Date
- 10/27/2026
- Time
- Before Open
- Conference Call
- Tuesday, October 27, 2026
Pharming Group's next earnings date is estimated for March 18, 2027, based on past reporting schedules.
Q3 2026 Earnings Call Audio
Q3 2026 Earnings Slide Deck
Q3 2026 Earnings Call Summary
The call was predominantly positive, supported by 21% third-quarter revenue growth, 58% Joenja growth, RUCONEST's return to revenue growth and stabilized U.S. demand, an 89% increase in operating profit, improved full-year guidance, strong liquidity, pediatric and international expansion, and encouraging clinical progress. The main challenges were the expected approximately 3% full-year decline in RUCONEST U.S. revenue, inventory-related timing effects, manufacturing inventory impairments, the unresolved CEO search, and prior FALCON site-activation delays.
For the full year 2026, revenue guidance was tightened to $380 million to $390 million, representing 14% growth, while operating expense guidance was lowered to $310 million to $315 million, representing 0% to 1% growth, including approximately $35 million incremental R&D investment and about $9 million of structural G&A savings; guidance assumes RUCONEST revenue will stabilize and return to growth in the second half of 26 and Joenja will deliver significant and accelerating growth, with RUCONEST U. S. Revenue expected to decline approximately 3% for the full year and Joenja annual revenue growth expected in the mid-30s%, while cost of goods sold is expected to be approximately 12% of revenue, corresponding to a gross margin of 88%, and Q4 revenue is implied to be roughly $100 million to $110 million; the company expects an initial bolus of new Joenja pediatric patients on therapy throughout Q4 in the range of 15 to 20 patients, expects 145 of the planned 180 FALCON participants to be enrolled by the end of this year, enrollment to be complete during the first half of 27, and top line results approximately 1 year after enrollment is complete, and expects to report top-line CVID results in November.
- Strong Third-Quarter Revenue GrowthThird-quarter revenue was $117.6 million, up 21% year over year and ahead of market expectations. Both commercial products contributed to growth.
- Joenja Delivered Robust GrowthGlobal Joenja revenue increased 58% year over year to $23.8 million. U.S. revenue rose 19% to $15.9 million, supported by continued growth in patients on therapy, while international revenue increased to $7.9 million from $1.7 million a year ago.
- Expansion of Joenja Patient Base and Geographic ReachThe company ended the quarter with 136 U.S. patients on paid therapy, up 17% year over year, and 75 international patients receiving paid therapy. Joenja launched in Germany in July and Japan in August, while continuing to penetrate the U.K.; international revenue represented approximately one-third of global Joenja revenue.
- U.S. Pediatric Joenja Approval and LaunchThe FDA approved Joenja's 40- and 50-milligram twice-daily doses for eligible children aged 4 to 11 weighing at least 27 kilograms on September 11, ahead of the anticipated October 24 PDUFA date. Shipments began in October, and the company expects an initial bolus of 15 to 20 pediatric patients on therapy throughout Q4.
- Further Pediatric Expansion Under Priority ReviewThe company submitted an application for lower Joenja doses for children aged 4 to 11 weighing between 13 and less than 27 kilograms. The FDA accepted the application with priority review and assigned a PDUFA date of January 30, 2027. More than 60 U.S. children aged 4 to 11 with APDS have been identified, with the currently approved doses addressing 38 of them.
- RUCONEST Returned to Revenue GrowthRUCONEST revenue reached $93.8 million in the third quarter, an increase of 14% year over year. Underlying U.S. demand stabilized, with volume returning to prior-year levels, and the company expects the positive demand trend to continue into Q4.
- Strong RUCONEST Patient RetentionThe company maintained more than 90% of its active RUCONEST patient base more than one year after the introduction of an oral on-demand competitor, with particularly strong retention among patients experiencing more frequent or severe HAE attacks. The company also continues to attract new patients and prescribers.
- Higher Operating Profit and Net ProfitThird-quarter operating profit increased 89% to $29.9 million. Excluding a $5.1 million one-time manufacturing-related inventory impairment, adjusted operating profit rose to $35 million from $16 million a year ago. Net profit increased to $22.4 million from $7.5 million.
- Strong Cash Generation and LiquidityThird-quarter operating cash flow was $32.4 million, and cash and marketable securities increased $31.4 million during the quarter to $190.9 million. Management stated that the cash position and future operating cash flows are expected to cover current pipeline and prelaunch costs, with no need to raise additional financing.
- Improved Full-Year GuidanceThe company tightened 2026 revenue guidance to $380 million to $390 million, representing 14% growth, and lowered operating expense guidance to $310 million to $315 million, representing 0% to 1% growth.
- Disciplined Expense Management with Continued R&D InvestmentOperating expenses were $74.6 million in the quarter, in line with the prior year, while nine-month total operating expenses were 2.8% below the prior year. Full-year guidance includes approximately $35 million of incremental R&D investment and approximately $9 million of structural G&A savings.
- Positive Leniolisib Genetic PID DataIn a 13-participant Phase 2 genetic PID study, 12 participants completed treatment. Leniolisib produced improvements in spleen volume, lymph node size, lung gas exchange, and liver stiffness, was well tolerated with no new safety signals, and all 12 participants who completed the study entered the three-year long-term extension study.
- CVID Development Program ProgressingThe company expects to report top-line results from its 20-patient CVID and CVID with immune dysregulation study in November. The results will assess lymphoproliferation, cytopenias, lung and liver disease, biomarkers, and safety, and will inform a potential registrational study. Regulatory interactions, including an end-of-Phase 2 meeting with the FDA, have already been planned.
- FALCON Study Passed Interim Futility AnalysisBoth primary endpoints in the pivotal FALCON study of nepasimone cleared a futility analysis after 40 patients completed 24 weeks of treatment. More than 50 sites are recruiting, the company expects 145 of the planned 180 participants to be enrolled by year-end, and enrollment is expected to be complete during the first half of 2027.
- Broader Commercial and Clinical OpportunityAs of September 30, the company had identified 304 U.S. APDS patients and 1.06 thousand globally. Management stated that international geographic expansion can result in a doubling of the addressable APDS opportunity, while the CVID population in the United States exceeds 13 thousand patients, or 26 times the APDS prevalence.
DE:PHG Earnings History
| Report Date | Fiscal Quarter | Forecast / EPS | Last Year's EPS | EPS YoY Change | Press Release |
|---|---|---|---|---|---|
| Mar 18, 2027 | 2026 (Q4) | 0.09- | 0.06 | ― | ― |
| Oct 27, 2026 | 2026 (Q3) | 0.190.27 | 0.09 | 200.00% (+0.18) | |
| Jul 30, 2026 | 2026 (Q2) | 0.060.02 | 0.05 | -66.67% (-0.04) | |
| May 07, 2026 | 2026 (Q1) | 0.00-0.06 | -0.2 | 68.18% (+0.13) | |
| Mar 12, 2026 | 2025 (Q4) | 0.010.06 | 0.04 | 40.00% (+0.02) | |
| Nov 06, 2025 | 2025 (Q3) | 0.000.09 | -0.02 | 600.00% (+0.11) | |
| Jul 31, 2025 | 2025 (Q2) | -0.090.05 | -0.02 | 400.00% (+0.07) | |
| May 08, 2025 | 2025 (Q1) | -0.02-0.20 | -0.17 | -15.79% (-0.03) | |
| Mar 13, 2025 | 2024 (Q4) | 0.020.04 | -0.04 | 225.00% (+0.08) | |
| Oct 24, 2024 | 2024 (Q3) | -0.00-0.02 | 0 | -500.00% (-0.02) |
The table shows recent earnings report dates and whether the forecast was beat or missed. See the change in forecast and EPS from the previous year.

