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Precigen (PGEN) investor relations material
Precigen Q1 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
PAPZIMEOS, approved in August 2025 as the first and only FDA-approved therapy for adults with RRP, achieved a landmark first commercial launch and is now the primary revenue driver, with rapid adoption across major medical centers and community practices.
Transitioned from a development-stage to a commercial-stage company, supported by strong payer coverage and a permanent J-code.
A landmark expert position paper and robust clinical data have established PAPZIMEOS as the new standard of care.
Patient hub enrollment reached approximately 400, with 25% from community settings, highlighting broad accessibility.
Strategic pipeline prioritization led to pausing enrollment in certain clinical trials and the shutdown of ActoBio operations.
Financial highlights
Q1 2026 net product revenue for PAPZIMEOS was $21.6 million, driving total Q1 2026 revenue to $23.3 million, up from $1.3 million in Q1 2025.
Net loss for Q1 2026 was $7.9 million ($0.02 per share), a significant improvement from $54.2 million ($0.18 per share) in Q1 2025.
R&D expenses were $5.6 million, down $4.8 million year-over-year, while SG&A expenses rose to $21 million, up $8.7 million due to commercialization.
Cash, cash equivalents, and investments totaled $56.7 million as of March 31, 2026, with Q1 cash used in operations at $43.8 million, including $13 million in non-recurring outflows.
Long-term debt stood at $93.5 million, with an effective interest rate of 12.5%.
Outlook and guidance
Expectation of continued revenue acceleration and account activation into Q2 and beyond, with strong payer coverage and community uptake.
Cash position and receivables projected to fund operations through cash flow break-even by end of 2026; no need for additional capital markets funding anticipated.
Management believes current liquidity and anticipated PAPZIMEOS revenue will fund operations for at least one year.
Additional investments planned for clinical and pre-clinical pipeline progression.
No specific Q2 guidance provided, but management highlights ongoing expansion and momentum.
- Shareholders will vote on director elections, auditor ratification, executive pay, and a key equity plan amendment.PGEN
Proxy filing30 Apr 2026 - Virtual meeting to vote on directors, auditor, compensation, and incentive plan amendment.PGEN
Proxy filing30 Apr 2026 - PAPZIMEOS sets a new standard for RRP, fueling growth and pipeline expansion via a unique platform.PGEN
Fireside chat3 Apr 2026 - PAPZIMEOS launch accelerates revenue growth and adoption, with Q1 2026 revenue set to exceed $18M.PGEN
Q4 202525 Mar 2026 - PAPZIMEOS launch accelerates adoption and revenue, but non-cash charges drive Q3 net loss.PGEN
Q3 20253 Feb 2026 - PRGN-2012 pivotal data and focus drive new funding, but losses and going concern risks persist.PGEN
Q2 20241 Feb 2026 - 51% complete response and 86% surgery reduction with durable benefit and strong safety.PGEN
Study Result31 Jan 2026 - FDA-approved RRP therapy saw rapid US uptake, strong brand growth, and global expansion plans.PGEN
44th Annual J.P. Morgan Healthcare Conference15 Jan 2026 - Gene therapy for RRP shows strong efficacy, safety, and commercial promise, with BLA submission imminent.PGEN
Stifel 2024 Healthcare Conference13 Jan 2026
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