Companies/EU/724500DCJ9MP

PHARMING GROUP N.V.

Last · Amsterdam€0.9586-0.0148 (-1.52%)stale · yahoo · 208h ago
Market cap€678.5M707.8M sh
P/E · TTM95.9fwd 44.1 · eps 0.01
Beta0.06vs S&P 500
Div yieldannual · TTM
52w range
€0.8338€1.818
Volume2.8Msession

Issuer

Legal namePHARMING GROUP N.V.
HQEurope (EU)
ListingEU 724500DCJ9MP
ISINNL0010391025
SectorHealthcare
IndustryPharmaceuticals
CurrencyUSD
Entity registrylei:724500DCJ9MPG74JEH91
Employees407
AddressPharming Group NV Vondellaan 47 2332 AA, Leiden +31 71 524 7400
Headline financial metrics
Revenue$376.1M
Operating income$25.8M
Net income$2.2M
Free cash flow$54.0M
Operating margin6.9%
Net margin0.6%
Return on equity0.8%
Period2025
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OpenFilings analyst

Our analyst

Agentic read of the latest earnings call — recommendation updates when we process a new transcript. Research synthesis, not investment advice.

Strong Joenja momentum is offset by competitive RUCONEST pressure, cash use, and unresolved execution and clinical risks.

Latest call · H1 2026

Hold: Pharming cut 2026 revenue guidance by $30 million to $375–395 million, implying 0%–5% growth, after RUCONEST revenue fell 10% year over year to $72.3 million in Q2.

Joenja remains the growth engine, up 40% to $17.9 million, but the investment case still depends on RUCONEST stabilizing, successful pediatric/geographic launches, and binary Q4 CVID/PID data; management did not quantify net RUCONEST patient gains when pressed.

Themes
  • Ruconest Competition
  • Joenja Growth
  • Pediatric Expansion
  • Germany Launch
  • Japan Launch
  • Cvid Phase Ii
+2

Near term

Q3 RUCONEST enrollments and revenue stabilization are the key test of management’s claim that the product will return to growth in the second half of 2026.

October 24 U.S. PDUFA decision on Joenja’s higher pediatric doses and submission of the lower-dose application could accelerate patient starts.

Germany’s launch and the planned August Japan launch should determine whether international Joenja growth can offset continued U.S. RUCONEST pressure.

Q4 readouts from the 20-patient CVID and 12-patient genetically defined PID Phase II studies are the largest near-term share-price catalyst.

Longer term

Joenja’s potential expansion from APDS into CVID could address a population management describes as up to 40 times larger, but approval would require further development, likely including a randomized Phase III trial.

RUCONEST retains a defensible niche among high-burden HAE patients, with 93% active-patient retention and 84 new enrollments in Q2, but the commercial franchise is no longer a dependable growth asset.

The pipeline could materially change Pharming’s scale through broader leniolisib indications and the 2027 napazimone FALCON readout, though both remain execution- and trial-dependent.

Operating discipline is improving, with full-year operating-expense guidance reduced to $315–320 million, but R&D investment remains elevated and growth is not yet translating into positive operating cash flow.

Red flags

Management declined to provide the net figure for RUCONEST new enrollments after switches and drop-offs when directly asked, leaving the underlying patient trajectory less clear than the 93% retention statistic suggests.

RUCONEST’s Q2 decline reflected ongoing U.S. competition, international-market withdrawals, and inventory normalization; management’s expected second-half stabilization is not yet demonstrated in reported revenue.

A $4.9 million RUCONEST manufacturing-inventory impairment remains unresolved; management said the review will not be concluded until the end of Q3 and some inventory may be unusable commercially.

Q2 operating cash flow was negative $9.7 million and H1 operating cash flow was negative $7.7 million, while cash and marketable securities fell to $159.5 million.

The broader CVID opportunity is based on small, open-label Phase II studies and encouraging clinician-reported experience; management expects a Phase III trial, so Q4 data would establish proof of concept rather than near-term revenue.

Forward outlook

revenue

375–395 $million

FY 2026

official guidance

revenue growth

0–5 pct

FY 2026

official guidance

revenue growth

-3 pct

FY 2026

official guidance

gross margin

89 pct

FY 2026

official guidance

Recommendation history

OpenFilings analyst view from primary-source filings and earnings calls — not investment advice.

From latest ANNUAL · 2025-04-15

  • Operating Cf Burn
  • Accumulated Deficit High

Red flags

  • Operating Cf Burn — Negative operating cash flow
  • Accumulated Deficit High — Accumulated deficit / equity 125%

Upcoming earnings

1 event
4:30 PM UTC+1
Period
Sep 2026
Est. EPS
$0.01
Est. revenue
104.1M

Earnings transcripts

12 of 25 recent

Press & signals

3 recent
  • GlobeNewswire

    FDA approves Pharming’s Joenja® as first treatment for children with APDS in the U.S.

  • GlobeNewswire

    Pharming announces commercial launch of Joenja (leniolisib) in Japan for adult and pediatric patients with APDS aged 4 and older

  • GlobeNewswire

    Pharming reports second quarter and first half 2026 financial results and revises year-end guidance; strong Joenja momentum and near-term clinical readouts to support broader therapeutic use

Documents

FormReporting forFiledFlags
2026-05-280
2026-05-280