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Catalyst Biosciences, Inc. (CBIO) is a clinical-stage biopharmaceutical innovator advancing protease-based therapies for hemophilia and related disorders. This news hub provides investors and healthcare stakeholders with timely updates on the company's scientific progress and operational developments.
Access curated announcements including clinical trial milestones, regulatory filings, and strategic partnership details. Our aggregation ensures you stay informed about Catalyst's pipeline advancements and financial initiatives without needing to monitor multiple sources.
Key updates cover therapeutic candidate progress, peer-reviewed research publications, and resource allocation strategies. All content is vetted for relevance to Catalyst's core mission of developing novel treatments for serious hematologic conditions.
Bookmark this page for streamlined access to Catalyst Biosciences' latest developments. Check back regularly for objective reporting on innovations in protease engineering and patient-focused therapeutic solutions.
Catalyst Biosciences, Inc. (NASDAQ: CBIO) will participate in a fireside chat at the Raymond James 42nd Annual Institutional Investors Conference on March 3, 2021, at 2:10 pm ET. Investors can access a live webcast of the event here. Catalyst focuses on rare disorders related to the complement and coagulation systems, with late-stage programs like MarzAA for bleeding disorders.
Catalyst Biosciences (NASDAQ:CBIO) announced the closing of an additional 485,000 shares at $5.75 each, netting approximately $2.8 million. The company aims to use these funds for general corporate needs, including research and development in hemophilia and complement programs, capital expenditures, and working capital.
Piper Sandler & Co. and Raymond James & Associates acted as bookrunners for the offering. This transaction follows an effective registration statement filed with the SEC in February 2019.
Catalyst Biosciences (NASDAQ: CBIO) announced positive pre-clinical findings for Marzeptacog alfa (activated) – MarzAA, at the EAHAD Congress on February 3, 2021. The next-gen engineered coagulation Factor VII demonstrated significant efficacy in controlling spontaneous bleeding in Hemophilia A rats and dogs. Most subjects required only a single subcutaneous dose for effective management. MarzAA is advancing to a Phase 3 trial for hemophilia patients. Catalyst aims to address unmet needs in bleeding disorders with its innovative therapies.
Catalyst Biosciences (NASDAQ:CBIO) has successfully closed an underwritten public offering of 8,700,000 shares at $5.75 each, raising approximately $50 million in gross proceeds. The funds will support general corporate purposes, including R&D in hemophilia and complement programs like MarzAA and CB 4332. The offering utilized an effective shelf registration with the SEC, showcasing Catalyst's ongoing commitment to address rare disorders. Piper Sandler & Co. served as the lead bookrunner for this offering.
Catalyst Biosciences, Inc. (NASDAQ:CBIO) announced a public offering of 8,700,000 shares at $5.75 each, with expected gross proceeds of $50 million. The offering includes a 30-day option for underwriters to purchase an additional 1,305,000 shares. Proceeds will support general corporate purposes, focusing on hemophilia and complement programs, including MarzAA and CB 4332. The offering is anticipated to close on January 29, 2021. Piper Sandler & Co. is the lead bookrunner.
Catalyst Biosciences (NASDAQ: CBIO) has announced an underwritten public offering of its common stock, with market conditions influencing the amount and terms. The company may grant underwriters a 30-day option to purchase an additional 15% of shares. Proceeds will support general corporate purposes, including research and development in hemophilia and complement programs, capital expenditures, and operational costs. The offering will use a previously filed effective registration statement. Piper Sandler & Co. and Raymond James & Associates are involved as bookrunners.
Catalyst Biosciences (NASDAQ: CBIO) announced two e-poster presentations at the EAHAD Virtual Congress occurring from February 3-5, 2021. The posters highlight the effectiveness of Marzeptacog Alfa (Activated) for treating spontaneous bleeding in both hemophilia A rats and dogs. Presenters include Tom Knudsen and Howard Levy, with accessible materials post-event on the Catalyst website.
Additionally, Catalyst is focused on developing solutions for rare coagulation disorders and has a partnership with Biogen for complement-related therapies.
Catalyst Biosciences, Inc. (NASDAQ: CBIO) announced participation in a fireside chat hosted by LifeSci Capital on January 19, 2021, at 1:00 pm ET. Management will discuss new complement programs and developments surrounding CB 2782, a C3 degrader partnered with Biogen, and MarzAA, a late-stage asset for hemostasis. The call registration can be accessed via email, with a replay available on the company's website for 90 days. Catalyst focuses on rare disorders of the complement and coagulation systems, boasting two late-stage clinical programs, including MarzAA.
Catalyst Biosciences (NASDAQ: CBIO) presented its Phase 3 study, Crimson 1, at the ASH meeting on December 7, 2020. The study evaluates Marzeptacog alfa (activated), a subcutaneous therapy for treating bleeding in patients with Hemophilia A or B with inhibitors. It aims to demonstrate non-inferiority compared to Standard of Care, enrolling about 60 subjects and treating 244 bleeding episodes. The primary endpoint is effective hemostasis at 24 hours. CEO Nassim Usman stated that MarzAA could be a significant addition to hemophilia treatment options.
Catalyst Biosciences, Inc. (NASDAQ: CBIO) will host a research and development call on December 14, 2020, at 12:00 pm ET regarding its systemic complement regulator programs. Management will introduce their first subcutaneously-dosed systemic complement candidate and provide insights on their protease engineering platform that targets various diseases. The call will feature Ronald P. Taylor, Ph.D., who will discuss complement-related diseases. This information will be available on their website for 90 days.