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Precigen (I5X) Q2 2026 Earnings Report

DE:I5X Q2 2026 EPS Results

Actual EPS
EUR 0.04
Consensus EPS
-EUR 0.01
Beat/Miss
Beat by +EUR 0.06
One Year Ago EPS
-EUR 0.08

DE:I5X Q2 2026 Revenue Results

Actual Revenue
EUR 49.16M
Expected Revenue
EUR 25.02M
Beat/Miss
Beat by +EUR 24.14M
YoY Revenue Growth
+6322.66%

Earnings Announcement Details

Quarter
Q2 2026
Date
08/04/2026
Time
After Close
Conference Call
Tuesday, August 4, 2026
DE:I5X Upcoming Earnings

Precigen's next earnings date is estimated for November 4, 2026, based on past reporting schedules.

Q2 2026 Earnings Call Audio

DE:I5X Q2 2026 Earnings Call
0:00 / 0:00

Q2 2026 Earnings Slide Deck

No slide deck is available for this earnings event.

Q2 2026 Earnings Call Summary

Q2 2026
Earnings Call Date:Aug 04, 2026|% Change Since:4.38%|
Earnings Call Sentiment|Positive

The call conveyed strong commercial momentum for PAPZIMEOS driven by exceptional Q2 revenue growth (>145% QoQ), launch-to-date revenue >$78M, broad payer coverage (~315M lives), durable clinical responses (83% ongoing CR >3 years), and attainment of profitability for the quarter and first half of 2026. Operational and financial risks noted include normalization of gross margins after remaining prelaunch inventory is consumed, reliance on accounts receivable collections and existing debt interest expense, rising commercial and future R&D spend, and limited public granularity on exact account activation counts and non-hub patient visibility. Overall, the positive revenue, profitability, coverage, and durability developments materially outweigh the manageable operational and financial caveats.

Company Guidance

Precigen guided that Q2 PAPZIMEOS revenue was $53.1M (Q1 $21.6M, >145% QoQ) and launch‑to‑date revenue exceeded $78M, with total Q2 revenues of $55M (COGS $2.8M; reported gross margin 95%); they expect gross margins to normalize to the high‑80% to low‑90% range after selling remaining pre‑approval inventory (anticipated in Q3). Financials/guidance included operating income of $22.6M, net income of $20.1M ($0.05/diluted), R&D $7.3M, SG&A $22.2M, cash and investments of $38.7M, trade receivables of $71.9M (expected to be collected over ~4 months), ~$100M debt with ~$3M quarterly interest (offset by ~ $0.4M interest income), and management’s view that cash + receivables will fund operations to cash‑flow breakeven by end‑2026. Commercial guidance/metrics: hub registrations >500, >200 patients have received ≥1 dose with >100 completing the 4‑dose course, ~315M covered lives after adding ~18M in Q2, permanent J‑code effective April 1, and 7‑year U.S. market exclusivity through August 2032.

  • Quarterly Revenue AccelerationPAPZIMEOS generated $53.1 million in Q2 revenue vs. $21.6 million in Q1, representing >145% quarter-over-quarter growth; total company revenues were $55.0 million for the quarter.
  • Profitability AchievedCompany reported operating income of $22.6 million and net income of $20.1 million (EPS $0.05) for Q2; Precigen achieved profitability for both the quarter and the six months ended June 30, prior to the first anniversary of FDA approval.
  • Launch-to-Date and Patient AdoptionLaunch-to-date PAPZIMEOS revenue exceeded $78 million at end of Q2. Commercial adoption indicators: Precigen Hub registrations exceed 500 patients; >200 patients have received at least one dose and >100 patients have completed the full 4-dose course.
  • High Reported Gross Margin (Near-Term)Q2 cost of products and services totaled $2.8 million yielding a reported gross margin of 95% (gross margin dollars ~$52.2 million); management expects steady-state gross margin to normalize in the high-80% to low-90% range after remaining prelaunch inventory is sold.
  • Broad Payer Coverage and Reimbursement SupportAdded ~18 million covered lives in Q2 bringing total commercial and government coverage to ~315 million lives in the U.S.; permanent J-code effective April 1 has aided account activation and reimbursement certainty.
  • Durability and Clinical DifferentiationDurability data (Apr 30 cutoff) show 83% of patients in ongoing complete response beyond 3 years, with several beyond 4 years and without any further RRP treatment since PAPZIMEOS—supporting a differentiated efficacy and durability profile.
  • Regulatory Protection and International ProgressFDA granted 7-year market exclusivity for adult RRP through August 2032; marketing authorization application under review by EMA and PAPZIMEOS has EU orphan drug designation.
  • Platform and Pipeline MomentumAdenoVerse platform validation highlighted by PAPZIMEOS success; PRGN-2009 advancing in multiple Phase II trials (head & neck and cervical cancer in combination with pembrolizumab) with an upcoming head & neck data update planned later this year.

DE:I5X Earnings History

DE:I5X earnings history
Report DateFiscal QuarterForecast / EPSLast Year's EPSEPS YoY ChangePress Release
Nov 04, 20262026 (Q3)0.05--0.95――
Aug 04, 20262026 (Q2)-0.010.04-0.08155.56% (+0.13)
May 13, 20262026 (Q1)-0.03-0.02-0.1688.89% (+0.14)
Mar 25, 20262025 (Q4)-0.08-0.06-0.075.41% (+0.00)
Nov 13, 20252025 (Q3)-0.08-0.95-0.08-1077.78% (-0.87)
Aug 12, 20252025 (Q2)-0.08-0.08-0.2160.87% (+0.13)
May 14, 20252025 (Q1)-0.12-0.16-0.09-80.00% (-0.07)
Mar 19, 20252024 (Q4)-0.05-0.07-0.1243.08% (+0.05)
Nov 14, 20242024 (Q3)-0.08-0.08-0.07-12.50% (-0.01)
Aug 14, 20242024 (Q2)-0.09-0.21-0.07-187.50% (-0.13)

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.

Beat Missed
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