24/7 Market News Snapshot 15 August, 2025 – Precigen, Inc. Common Stock (NASDAQ:PGEN)

DENVER, Colo., 15 August, 2025 (www.247marketnews.com) – (NASDAQ:PGEN) are discussed in this article.
Precigen, Inc. has recently achieved a significant milestone with the FDA’s approval of PAPZIMEOS™ (zopapogene imadenovec-drba) for the treatment of recurrent respiratory papillomatosis (RRP), the first-ever therapy specifically targeting this rare and challenging condition affecting adults. Priced at $3.278, Precigen’s stock surged by an impressive 77.19% in pre-market trading, reflecting heightened investor interest and optimism surrounding this breakthrough. With a trading volume of 5.06 million shares, the market response underscores the positive outlook for the biotechnology firm.

PAPZIMEOS employs a novel, non-replicating adenoviral vector-based immunotherapy designed to enhance the immune response against papilloma cells associated with human papillomavirus (HPV) types 6 and 11, the primary cause of RRP. This innovative treatment not only addresses the underlying viral infection but is also anticipated to drastically reduce the frequency of surgical interventions often required in traditional management approaches. Data from pivotal trials demonstrated that 51% of participants reached a Complete Response, suggesting a considerable impact on patient quality of life.

Dr. Helen Sabzevari, President and CEO of Precigen, emphasized the import of this approval as a transformative development for adult patients who have faced prolonged challenges with RRP. “We are committed to bringing PAPZIMEOS to the RRP community, offering a viable therapeutic option that moves beyond repetitive surgeries,” she stated.

To facilitate patient access, Precigen is launching a comprehensive support program and plans to hold a conference call to outline further steps following this promising approval. The company’s achievements signal a forward-thinking approach and bolster its position as a leader in innovative healthcare solutions, marking the beginning of a new chapter for those managing RRP in the United States.

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