Welcome to our dedicated page for Pmv Pharmaceuticals news (Ticker: PMVP), a resource for investors and traders seeking the latest updates and insights on Pmv Pharmaceuticals stock.
PMV Pharmaceuticals, Inc. (PMVP) is a clinical-stage biopharmaceutical company pioneering precision oncology therapies targeting p53 mutations, a key driver in many cancers. This page provides investors and researchers with verified updates on clinical trials, regulatory milestones, and corporate developments.
Access real-time announcements including phase progressions for PC14586 and other pipeline candidates, financial disclosures, and strategic collaborations. Our curated repository ensures you stay informed about PMVP’s tumor-agnostic approach to reactivating p53’s tumor-suppressing function.
Key updates cover clinical data publications, FDA designations, and research partnerships advancing small-molecule therapeutics. Bookmark this page for streamlined access to PMVP’s progress in developing treatments that address unmet needs in genetically defined cancers.
PMV Pharmaceuticals announced its participation at the AACR Annual Meeting 2021 from April 10-15, where it will present on PC14586, the first orally bioavailable small molecule reactivator of the Y220C mutant p53. This therapy targets a significant mutation found in various cancers, aiming to restore the tumor suppressor function of p53. Details of the presentation include the title, authors, and timing. PMV aims to develop this innovative treatment for patients with advanced solid tumors.
PMV Pharmaceuticals, Inc. (Nasdaq: PMVP) has initiated a Phase 1/2 study of PC14586, targeting advanced solid tumors with a p53 Y220C mutation. The FDA granted Fast Track designation for this investigational therapy. Financially, the company reported a net loss of $34.4 million for 2020, up from $25.4 million in 2019. PMVP ended Q4 2020 with $361.4 million in cash, a significant increase from $101.5 million a year earlier. R&D expenses rose to $23.9 million due to clinical advances, while G&A expenses increased to $11 million as the company expands its public operations.
PMV Pharmaceuticals (Nasdaq: PMVP) announced its participation in the Lung Cancer Panel at the Cowen 41st Annual Health Care Conference from March 1-4, 2021. David H. Mack, Ph.D., CEO, will speak on March 2 at 11:10 AM. PMV Pharma focuses on developing small molecule, tumor-agnostic therapies targeting p53 mutations, prevalent in about half of all cancers. The company's foundation is rooted in over four decades of p53 biology research by co-founder Dr. Arnold Levine.
PMV Pharmaceuticals, Inc. (Nasdaq: PMVP) appointed Dr. Guillermina (Gigi) Lozano to its Scientific Advisory Board, enhancing its expertise in p53 biology. Dr. Lozano, a distinguished geneticist, has made significant contributions to understanding the p53 pathway and its mutations in cancer. Her experience at The University of Texas MD Anderson Cancer Center and recognition from acclaimed scientific organizations underscore her qualifications. This strategic addition could bolster PMV Pharma's efforts in developing small molecule therapies targeting p53 mutations, which are prevalent in nearly half of all cancers.
PMV Pharmaceuticals (Nasdaq: PMVP) has announced that CEO David H. Mack, Ph.D., will present at the Evercore ISI 3rd Annual HealthCONx Conference on December 2, 2020, at 1:00 PM ET. This presentation focuses on the company's pioneering work in precision oncology, targeting p53 mutants, a common mutation in cancer. Interested parties can access the presentation via the company's website. PMV Pharma, based in Cranbury, New Jersey, specializes in tumor-agnostic therapies and is leveraging decades of research in p53 biology.
PMV Pharmaceuticals (Nasdaq: PMVP) has initiated a Phase 1/2 clinical trial for PC14586, targeting patients with advanced solid tumors featuring the p53 Y220C mutation. This therapy aims to reactivate the tumor-suppressing function of the p53 protein, which is crucial in cancer prevention. The trial will enroll up to 130 patients and assess safety, tolerability, and anti-tumor activity. With PC14586 having received Fast Track Designation from the FDA, this represents a significant milestone for PMVP in addressing the unmet medical needs of patients with this specific mutation.
PMV Pharmaceuticals (NASDAQ: PMVP) achieved significant milestones, including FDA clearance for its investigational new drug PC14586, aimed at treating solid tumors with the p53 Y220C mutation. The company raised approximately $243.5 million through its IPO, optimizing its capital to further clinical development and expand its discovery pipeline. PMVP reported third-quarter results with $373.1 million in cash, a net loss of $8.8 million, and a rise in R&D and G&A expenses compared to the previous year. Fast Track designation from the FDA also enhances the development pace of PC14586.
PMV Pharmaceuticals announced that the FDA has granted Fast Track designation to its lead candidate, PC14586, aimed at treating cancer patients with a specific p53 Y220C mutation. This designation highlights the potential of PC14586 to meet a critical medical need, as there are no current FDA-approved therapies targeting this mutation found in various cancers. The planned Phase 1/2 studies will assess the drug's safety and efficacy in patients with locally advanced or metastatic solid tumors. Overall, this development could significantly enhance treatment options for patients facing poor outcomes due to p53 mutations.
PMV Pharmaceuticals has successfully closed its initial public offering, selling 13,529,750 shares of common stock at a price of $18.00 per share, generating approximately $243.5 million in gross proceeds. The offering included 1,764,750 additional shares exercised by underwriters. PMV Pharma focuses on small molecule therapies targeting p53 mutations, which are prevalent in nearly 50% of all cancers. The company is listed on the Nasdaq under the ticker symbol 'PMVP' and aims to leverage funds for further development in precision oncology.
PMV Pharmaceuticals, Inc. has successfully closed its initial public offering, selling 13,529,750 shares at $18.00 each, raising approximately $243.5 million in gross proceeds. The offering included the underwriters' full exercise of their option to purchase an additional 1,764,750 shares. The offering was registered with the SEC, effective September 24, 2020, and all shares were offered by PMV Pharma. Goldman Sachs, BofA Securities, Cowen, and Evercore ISI acted as joint book-running managers for this offering. PMV Pharma focuses on developing therapies targeting p53 mutations found in many cancers.