Precigen's Recurrent Respiratory Papillomatosis Drug Gets FDA Approval, Shares Surge
PorAinvest
viernes, 15 de agosto de 2025, 6:36 am ET1 min de lectura
PGEN--
Papzimeos, previously known as PRGN-2012, is designed to address RRP, a rare and intractable disease caused by persistent human papillomavirus infection. The condition leads to the growth of benign tumors in the respiratory tract, often in the larynx. The FDA granted the drug priority review in February, with a target action date of Aug. 27 [1].
Precigen's proprietary technology platforms have been instrumental in advancing its pipeline, which includes therapies across multiple indications. The company's operations span biopharmaceuticals and exemplar segments, reflecting its commitment to addressing complex medical challenges. The recent FDA approval underscores Precigen's potential to make a meaningful impact in the treatment of rare diseases.
The stock's pre-bell surge highlights investor confidence in Precigen's ability to translate its innovative technologies into market-ready treatments. As the company continues to advance its pipeline, investors will be closely monitoring its progress in immuno-oncology, autoimmune disorders, and infectious diseases.
References:
[1] https://www.tradingview.com/news/DJN_DN20250814014047:0-precigen-gets-fda-approval-of-respiratory-tumor-treatment/
Precigen's shares surged pre-bell after the FDA approved its drug for recurrent respiratory papillomatosis, a rare and intractable disease. The biopharmaceutical company's proprietary technology platforms develop product candidates for immuno-oncology, autoimmune disorders, and infectious diseases. Its pipeline includes therapies across multiple indications, with operations in biopharmaceuticals and exemplar segments.
Precigen's stock experienced a significant pre-bell rally following the Food and Drug Administration's (FDA) approval of its lead product candidate, Papzimeos, for the treatment of adults with recurrent respiratory papillomatosis (RRP). The approval marks a notable milestone for the biopharmaceutical company, which specializes in developing product candidates for immuno-oncology, autoimmune disorders, and infectious diseases [1].Papzimeos, previously known as PRGN-2012, is designed to address RRP, a rare and intractable disease caused by persistent human papillomavirus infection. The condition leads to the growth of benign tumors in the respiratory tract, often in the larynx. The FDA granted the drug priority review in February, with a target action date of Aug. 27 [1].
Precigen's proprietary technology platforms have been instrumental in advancing its pipeline, which includes therapies across multiple indications. The company's operations span biopharmaceuticals and exemplar segments, reflecting its commitment to addressing complex medical challenges. The recent FDA approval underscores Precigen's potential to make a meaningful impact in the treatment of rare diseases.
The stock's pre-bell surge highlights investor confidence in Precigen's ability to translate its innovative technologies into market-ready treatments. As the company continues to advance its pipeline, investors will be closely monitoring its progress in immuno-oncology, autoimmune disorders, and infectious diseases.
References:
[1] https://www.tradingview.com/news/DJN_DN20250814014047:0-precigen-gets-fda-approval-of-respiratory-tumor-treatment/

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