Welcome to our dedicated page for Crescent Biopharma news (Ticker: CBIO), a resource for investors and traders seeking the latest updates and insights on Crescent Biopharma stock.
Crescent Biopharma reports news about its clinical-stage oncology pipeline, including CR-001, a PD-1 x VEGF bispecific antibody, and antibody-drug conjugate programs such as CR-002 and CR-003. Company updates commonly cover clinical trial activity in solid tumors, pipeline combinations, collaboration activity, financial results, and business highlights.
Recurring corporate announcements also include investor conference presentations and equity inducement awards under the company’s employment inducement incentive plan. These updates reflect Crescent’s status as a Nasdaq-listed biotechnology issuer focused on cancer therapeutics.
Catalyst Biosciences, Inc. (NASDAQ: CBIO) reported its third-quarter results for 2020, ending September 30. The net loss was $16 million, equating to ($0.73) per share, an improvement from a loss of $12.7 million or ($1.06) per share in Q3 2019. The company is advancing clinical trials for its MarzAA product and expects to enroll patients in a Phase 3 study for hemophilia treatment by year-end. Cash and investments totaled $104.1 million. Additionally, Catalyst secured a patent for its complement program, providing protection until at least 2038.
Catalyst Biosciences (NASDAQ: CBIO) announced its participation in the Stifel 2020 Virtual Healthcare Conference, scheduled for November 17, 2020, at 11:20 am ET. Presenters include CEO Nassim Usman, Ph.D., and CFO Clinton Musil. The presentation can be accessed via a webcast, and will remain available for 90 days post-event on the company’s website. Catalyst focuses on developing novel therapies for rare hematologic and complement-mediated disorders, leveraging advanced protease engineering technology.
Catalyst Biosciences has secured an extension of patent protection for CB 2782-PEG until at least 2038, enhancing its market position. The patent covers engineered proteases that target complement factor 3 (C3), with therapeutic potential for conditions like dry age-related macular degeneration (AMD). Catalyst’s partnership with Biogen for CB 2782-PEG emphasizes its clinical significance. The announcement comes alongside an emphasis on expanding clinical candidates from their protease engineering platform, underscoring ongoing innovation within the company.
Catalyst Biosciences, based in South San Francisco, announced that Dr. Grant Blouse will present at the Stifel Immunology and Inflammation Virtual Summit on October 1, 2020, at 9:00 AM ET. He will discuss the evolution of complement-targeted therapies. Interested participants can access the live presentation via a provided link, with an archived version available for 90 days post-event. Catalyst is focused on biopharmaceutical developments, particularly in rare hematologic disorders, with advanced clinical programs, including marzeptacog alfa and dalcinonacog alfa.
Catalyst Biosciences (NASDAQ: CBIO) announced participation in two investor conferences on September 17, 2020. The Morgan Stanley Global Healthcare Conference will feature CEO Nassim Usman and CFO Clinton Musil at 5:00 PM ET, with a webcast available. Concurrently, they will present at the Cantor Virtual Global Healthcare Conference at 4:40 PM ET, with a separate webcast.
Catalyst Biosciences (NASDAQ: CBIO) reported notable advancements and financial outcomes for Q2 2020, ending June 30, 2020. The company holds approximately $117 million in cash, supporting ongoing pipeline development, including pivotal Phase 3 trials of MarzAA for hemophilia. The quarterly net loss was $17.2 million, with a loss per share of $0.96, compared to a loss of $13.8 million and $1.15 per share in Q2 2019. R&D expenses increased by 16% to $12.9 million. Catalyst aims to initiate further trials and identify candidates in its gene therapy and complement programs by late 2020.
Catalyst Biosciences (NASDAQ: CBIO) presented data regarding marzeptacog alfa (activated) (MarzAA) at the ISTH Virtual Congress. The Phase 1 study showed that MarzAA quickly achieves therapeutic levels for treating acute bleeding in hemophilia patients. A Population PK model confirmed effective dosing for the upcoming Phase 3 trial, Crimson 1, set to start in late 2020. The results suggest a significant market opportunity for MarzAA, addressing a crucial need in bleeding disorder treatments.
Catalyst Biosciences (NASDAQ: CBIO) announced that Clinton Musil has been granted a non-qualified stock option to purchase 140,000 shares of common stock. This is part of his inducement package as the new Chief Financial Officer, effective July 1, 2020. The option has a ten-year term with an exercise price of $5.88 and will vest over four years. Catalyst focuses on developing treatments for rare hematologic conditions and has multiple clinical programs, including MarzAA, a next-generation treatment for hemophilia, set for a Phase 3 study in late 2020.
Catalyst Biosciences (NASDAQ:CBIO) has been added to the Russell 2000 Index effective June 29, 2020. This inclusion, resulting from the Russell index reconstitution, ranks the company among the 4,000 largest U.S. stocks based on market capitalization. Membership in the Russell 2000 also means inclusion in growth and value style indices. Russell indices are widely used by investment managers, with approximately $9 trillion in assets benchmarked against them. Catalyst is focused on innovative treatments for rare hematologic disorders, utilizing its proprietary protease engineering platform.
Catalyst Biosciences (NASDAQ: CBIO) announced two presentations at the International Society on Thrombosis and Haemostasis (ISTH) Virtual Congress, scheduled for July 12-14, 2020. The presentations will focus on marzeptacog alfa (activated), a next-generation treatment for hemophilia. Key topics include a Phase 1 study detailing pharmacokinetics and safety, and population pharmacokinetics simulations for dose selection in Phase 3 trials. Catalyst aims to address unmet needs in rare hematologic disorders with its protease engineering platform, and its lead candidate is set for a Phase 3 study later this year.