Precigen, Inc. (PGEN)

NASDAQ: PGEN · Real-Time Price · USD
4.130
+0.170 (4.29%)
At close: Apr 24, 2026, 4:00 PM EDT
4.200
+0.070 (1.69%)
After-hours: Apr 24, 2026, 7:45 PM EDT
Market Cap1.46B +257.7%
Revenue (ttm)9.68M +146.7%
Net Income-429.64M
EPS-1.37
Shares Out 353.93M
PE Ration/a
Forward PEn/a
Dividendn/a
Ex-Dividend Daten/a
Volume3,459,179
Open4.000
Previous Close3.960
Day's Range3.950 - 4.260
52-Week Range1.225 - 5.465
Beta1.12
AnalystsBuy
Price Target8.33 (+101.7%)
Earnings DateMay 13, 2026

About PGEN

Precigen, Inc.,a discovery and clinical-stage biopharmaceutical company, develops gene and cell therapies using precision technology to target diseases in areas of immuno-oncology, autoimmune disorders, and infectious diseases. The company offers therapeutic platforms consisting of AdenoVerse platform, which utilizes a library of proprietary adenovectors for gene delivery of therapeutic effectors, immunomodulators, and vaccine antigen; and UltraCAR-T to provide chimeric antigen receptor T cell therapies for cancer patients. It also develops pro... [Read more]

Industry Biotechnology
Sector Healthcare
Founded 1998
Employees 160
Stock Exchange NASDAQ
Ticker Symbol PGEN
Full Company Profile

Financial Performance

In 2025, Precigen's revenue was $9.68 million, an increase of 146.73% compared to the previous year's $3.93 million. Losses were -$429.64 million, 240.4% more than in 2024.

Financial Statements

Analyst Summary

According to 5 analysts, the average rating for PGEN stock is "Buy." The 12-month stock price target is $8.33, which is an increase of 101.70% from the latest price.

Price Target
$8.33
(101.70% upside)
Analyst Consensus: Buy
Stock Forecasts

News

Precigen Reports 'Robust Uptake' of New Drug for Rare Respiratory Disease; First Quarter Revenue Expected to Top $18 Million

Plans Underway to Expand Use to Pediatrics, Patient Redosing and European Approval Meg Flippin, Benzinga Staff Writer GERMANTOWN, MD / ACCESS Newswire / April 7, 2026 / Precigen Inc. (NASDAQ:PGEN), a ...

19 days ago - Accesswire

Precigen Transcript: Fireside chat

PAPZIMEOS, the first immunotherapy for adult RRP, is driving a commercial transformation, with strong launch metrics, broad physician support, and robust payer access. The company is expanding its pip...

25 days ago - Transcripts

Precigen to Participate in a Fireside Chat with H.C. Wainwright on March 31

GERMANTOWN, Md., March 30, 2026 /PRNewswire/ -- Precigen, Inc. (Nasdaq: PGEN), a commercial-stage biopharmaceutical company specializing in the advancement of innovative precision medicines to improve...

27 days ago - PRNewsWire

These Analysts Boost Their Forecasts On Precigen Following Q4 Results

Precigen, Inc. (NASDAQ: PGEN) reported mixed results for the fourth quarter on Wednesday.

4 weeks ago - Benzinga

Precigen Earnings Call Transcript: Q4 2025

PAPZIMEOS launch drove a 149% revenue increase in 2025, with Q1 2026 revenue expected to exceed $18 million. Broad payer coverage, strong physician uptake, and a permanent J-code are accelerating adop...

4 weeks ago - Transcripts

Precigen Reports Full Year 2025 Financial Results and Business Updates

Precigen transitioned to a commercial stage company with the US approval of PAPZIMEOS™ (zopapogene imadenovec-drba), the first-and-only FDA-approved treatment for adults with RRP, in August 2025 PAPZI...

4 weeks ago - PRNewsWire

Precigen to Announce Full Year 2025 Financial Results and Provide Business Updates on March 25

GERMANTOWN, Md., March 11, 2026 /PRNewswire/ -- Precigen, Inc. (Nasdaq: PGEN), a commercial-stage biopharmaceutical company specializing in the advancement of innovative precision medicines to improve...

6 weeks ago - PRNewsWire

New Expert Consensus Published in The Laryngoscope Recommends PAPZIMEOS (zopapogene imadenovec) as the New Standard of Care First-Line Treatment for Adults with Recurrent Respiratory Papillomatosis

Independent, expert-led consensus paper, sponsored by the Recurrent Respiratory Papillomatosis Foundation, reflects the recommendation of 16 leading physicians in the field of RRP Consensus paper reco...

3 months ago - PRNewsWire

Precigen Transcript: 44th Annual J.P. Morgan Healthcare Conference

A proprietary adenovirus platform enabled rapid development and full FDA approval of Pepcimeus for RRP, shifting care from surgery to a medical standard. Commercial launch saw swift market penetration...

3 months ago - Transcripts

Precigen Showcases Rapid Commercialization Momentum and Growing Market Adoption of First-and-Only FDA-Approved Therapy for RRP at the 44th Annual J.P. Morgan Healthcare Conference

Precigen transitioned to a commercial stage company with the US approval of PAPZIMEOS in August 2025, the first-and-only FDA-approved treatment for adults with RRP PAPZIMEOS commercialization is well ...

3 months ago - PRNewsWire

Precigen to Present at the 44th Annual J.P. Morgan Healthcare Conference

GERMANTOWN, Md., Jan. 5, 2026 /PRNewswire/ -- Precigen, Inc. (Nasdaq: PGEN), a biopharmaceutical company advancing innovative precision medicines, today announced that Helen Sabzevari, PhD, President ...

3 months ago - PRNewsWire

Precigen Earnings Call Transcript: Q3 2025

PAPZIMEOS secured full FDA approval and launched as the first therapy for adult RRP, showing strong efficacy, safety, and rapid commercial uptake. Q3 ended with $123.6M in cash, and breakeven is targe...

5 months ago - Transcripts

Precigen Reports Third Quarter 2025 Financial Results and Business Updates

PAPZIMEOS (zopapogene imadenovec-drba) received full approval by the FDA in August PAPZIMEOS launched with a broad label in the US as the first and only FDA-approved treatment for adults with RRP PAPZ...

5 months ago - PRNewsWire

Precigen to Announce Third Quarter 2025 Financial Results and Provide Business Updates on November 13

GERMANTOWN, Md. , Nov. 6, 2025 /PRNewswire/ -- Precigen, Inc. (Nasdaq: PGEN), a biopharmaceutical company specializing in the advancement of innovative precision medicines to improve the lives of pati...

6 months ago - PRNewsWire

Precigen Announces Long-Term Follow-Up Results Highlighting Ongoing Durable Complete Responses after Treatment with PAPZIMEOS, the First and Only FDA-approved Therapy for Adults with Recurrent Respiratory Papillomatosis

15 out of 18 complete responders (83%) demonstrate continued complete response with median follow-up of 36 months Reduction in surgeries compared to year prior to treatment with PAPZIMEOS was observed...

6 months ago - PRNewsWire

Precigen Announces Up to $125 Million Non-Dilutive Financing

$100 million funded at close fortifies balance sheet and supports robust US commercialization of PAPZIMEOS, as well as potential expansion into international markets and the pursuit of pediatric and o...

8 months ago - PRNewsWire

Precigen Transcript: Fireside Chat

PAPZIMEOS, a first-in-class therapy for recurrent respiratory papillomatosis, received early FDA approval and is set for a broad U.S. launch. The company is expanding indications, has a strong financi...

8 months ago - Transcripts

Precigen to Participate in Upcoming Virtual Fireside Chats Hosted by Cantor and H.C. Wainwright

GERMANTOWN, Md. , Aug. 25, 2025 /PRNewswire/ -- Precigen, Inc. (Nasdaq: PGEN), a biopharmaceutical company specializing in the advancement of innovative precision medicines to improve the lives of pat...

8 months ago - PRNewsWire

Precigen Transcript: Investor Update

Papzimeos received full FDA approval as the first and only therapy for adult RRP, with a broad label and strong efficacy. The launch targets over 90% of the patient population, supported by robust inf...

8 months ago - Transcripts

Why Is Precigen Stock Surging On Friday?

On Friday, the U.S. Food and Drug Administration (FDA) approved Precigen Inc.'s PGEN Papzimeos (zopapogene imadenovec-drba) for adult patients with recurrent respiratory papillomatosis (RRP).

9 months ago - Benzinga

US FDA approves Precigen's immunotherapy for rare respiratory disease

The U.S. Food and Drug Administration has approved Precigen's immunotherapy to treat adults with a rare respiratory disease, making it the first treatment for the condition to receive the health regul...

9 months ago - Reuters

Precigen Announces Full FDA Approval of PAPZIMEOS (zopapogene imadenovec-drba), the First and Only Approved Therapy for the Treatment of Adults with Recurrent Respiratory Papillomatosis

PAPZIMEOS approval marks a historic milestone for the RRP patient community as the first and only FDA-approved therapy for the treatment of adults with RRP PAPZIMEOS received full approval from the FD...

9 months ago - PRNewsWire

Precigen Reports First Quarter 2025 Financial Results and Business Updates

PRGN-2012 has the potential to be the first- and best-in-class treatment for RRP Company's BLA for PRGN-2012 for the treatment of adults with RRP is under priority review by the FDA with a PDUFA targe...

1 year ago - PRNewsWire

Precigen and Recurrent Respiratory Papillomatosis Foundation to Host the 2025 International RRP Awareness Day on June 11th

– International event will raise awareness and bring together RRP patients , caregivers, and the healthcare community supporting them – – Recurrent respiratory papillomatosis is a rare, debilitating, ...

1 year ago - PRNewsWire

Precigen Earnings Call Transcript: Q4 2024

PRGN-2012 advanced rapidly to FDA priority review, with pivotal data showing 51% durable complete response in RRP. Financially, a $126.2M net loss was offset by new funding, supporting operations into...

1 year ago - Transcripts