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Precigen (PGEN) investor relations material
Precigen 44th Annual J.P. Morgan Healthcare Conference summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Portfolio and Technology Advancements
Focus on differentiated cell and gene therapy platforms, including a proprietary gorilla adenovirus vector with high payload capacity, repeat dosing, and full IP protection.
Platform enables strong T cell immunity, minimal seropositivity, and supports multiple injections over years without loss of efficacy.
In-house manufacturing enables rapid development and commercialization.
Lead product (Pepcimeus/PAPZIMEOS) approved for recurrent respiratory papillomatosis (RRP), with additional candidates in phase II for HPV-related cancers.
Ongoing platform expansion through PRGN-2009 in head and neck and cervical cancers.
Commercialization and Market Execution
Pepcimeus/PAPZIMEOS received full FDA approval in August 2025 for all adult RRP patients, regardless of disease severity, shifting care from surgery to medical management.
U.S. commercial launch executed rapidly, with over 96% of target centers covered and strong payer uptake (170 million lives covered, ~80% of market).
Significant increase in brand awareness among physicians and patients within three months post-approval, with unaided awareness rising sharply in both academic and community settings.
Patient support hub established, with over 200 patients registered and parallel uptake through centers of excellence and community practices.
Broad FDA label allows use across all severities and stages of RRP, supporting early intervention and reducing irreversible damage.
Clinical Data and Patient Impact
Pivotal trials showed a 51% complete response rate, with complete responders having zero surgeries after four injections over three months and durable responses beyond three years.
Partial responders saw reduced surgery frequency; safety profile comparable to a flu shot.
Addresses a large unmet need: 27,000 U.S. patients, 35,000+ in Europe/Japan, 85,000+ in China.
Early and broad adoption driven by physician and patient demand to avoid surgical interventions and irreversible harm.
Enables repeat administration and is designed to generate a targeted immune response against HPV 6/11.
- TimeTickerHeadlineOpen
- 7 FebPGIL
Strong 9MFY26 growth with 13.2% higher revenue, margin gains, and upgraded credit ratings. - 7 Feb504614
Strong revenue and profit growth in Q3 FY26, led by power and steel segments. - 7 FebCHEMPLASTS
Net losses widened and revenue fell year-over-year amid regulatory and market headwinds. - 7 FebSBIN
Q3 FY26 net profit reached ₹21,028.15 crore, driven by robust income and strategic divestments. - 6 FebHTOO
Resale registration for 71,429 shares via warrant, with proceeds only on exercise; financial risks persist. - 6 FebVSAT
Q3 revenue up 3% to $1.16B, net income $25M, strong cash flow, Ligado boost, satellite focus. - 6 FebWEC
Targets 7–8% EPS growth, $37.5B capex, and coal exit by 2032 amid surging data center demand. - 6 FebBR
Q2 FY26 recurring revenue grew 8% and adjusted EPS guidance was raised to 9-12%. - 6 FebFFWM
Merger vote includes new non-voting stock class with limited conversion and no voting rights. - 6 FebKKR
Charter amendments seek to modernize governance and establish one share, one vote by 2026.
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