Welcome to our dedicated page for C4 Therapeutics news (Ticker: CCCC), a resource for investors and traders seeking the latest updates and insights on C4 Therapeutics stock.
C4 Therapeutics, Inc. (C4T) (Nasdaq: CCCC) is a clinical-stage biopharmaceutical company focused on targeted protein degradation, and its news flow reflects active clinical development, collaborations and capital markets activity. Company updates frequently highlight progress with cemsidomide, an investigational IKZF1/3 degrader in development for relapsed/refractory multiple myeloma and certain lymphomas, as well as broader pipeline and platform achievements.
News for C4 Therapeutics often centers on clinical data milestones, such as Phase 1 results for cemsidomide in combination with dexamethasone, acceptance of data for oral presentation at scientific meetings, and plans for registrational trials like the Phase 2 MOMENTUM study. Releases also cover developments in non-Hodgkins lymphoma cohorts and updates on other degrader programs, including CFT8919 for EGFR-mutant non-small cell lung cancer and CFT1946 for BRAF V600 mutant solid tumors.
Investors following CCCC news will also see collaboration announcements and research milestones. Examples include the clinical trial collaboration and supply agreement with Pfizer to evaluate cemsidomide with elranatamab in multiple myeloma, milestone achievements in partnerships with Biogen, Roche and Merck KGaA, Darmstadt, Germany, and regulatory steps such as IND acceptance for BIIB142, an IRAK4 degrader designed by C4 Therapeutics.
Financial and corporate updates are another key news category. The company regularly reports quarterly financial results, cash runway guidance, equity offerings and changes to its capital structure via press releases and Form 8-K filings. For readers tracking CCCC, this news page aggregates these clinical, scientific, collaboration and financing updates in one place, making it easier to monitor how C4 Therapeutics is advancing its targeted protein degradation pipeline over time.
C4 Therapeutics (Nasdaq: CCCC) reported significant advancements in their clinical programs and financials for Q2 2021. They initiated the Phase 1/2 trial of CFT7455 for hematologic malignancies and received Orphan Drug Designation from the FDA for this therapy. The company reported Q2 revenue of $9.8 million, a slight increase from $9.7 million in the previous year, and a net loss of $22.6 million, up from $10.8 million. A successful public offering yielded $180.8 million, bolstering cash reserves to approximately $499 million by June 30, 2021, supporting their ambitious clinical development plans.
C4 Therapeutics, Inc. (Nasdaq: CCCC) announced that the FDA granted orphan drug designation to its drug CFT7455 for treating multiple myeloma. This designation supports clinical development and provides potential market exclusivity in the U.S. Moreover, CFT7455 is designed to selectively target disease-causing proteins, with an ongoing Phase 1/2 trial aimed at evaluating its safety and anti-tumor activity, intending to enroll approximately 160 patients. C4 Therapeutics aims to improve outcomes for multiple myeloma patients who currently face limited treatment options.
C4 Therapeutics (Nasdaq: CCCC) announced the closing of an underwritten public offering of 4,887,500 shares at $37.00 per share, raising about $180.8 million in gross proceeds. This includes the full exercise of the underwriters' option for an additional 637,500 shares. The offering was managed by J.P. Morgan, Jefferies, Evercore ISI, BMO Capital Markets, and UBS Investment Bank. The funds will be directed towards advancing the company’s innovative small-molecule medicines aimed at degrading disease-causing proteins, a strategy that could potentially enhance cancer treatments.
C4 Therapeutics (Nasdaq: CCCC) presented promising pre-clinical data for its lead compound, CFT7455, at the ICML conference. This orally bioavailable MonoDAC™ demonstrated high binding affinity to cereblon and effective IKZF1/3 degradation in non-Hodgkin’s lymphoma (NHL) models. CFT7455 showed superior efficacy in xenograft models compared to approved therapies, including significant tumor regressions in various NHL subtypes. The Phase 1/2 trial, initiated in June 2021, aims to further assess CFT7455’s potential against multiple myeloma and NHLs, with top-line results expected in 2022.
C4 Therapeutics, Inc. (Nasdaq: CCCC) has announced the pricing of a public offering of 4.25 million shares of common stock at $37.00 each. The offering, expected to yield approximately $157 million in gross proceeds, is set to close around June 21, 2021, pending customary conditions. An option for underwriters to purchase an additional 637,500 shares is included. J.P. Morgan, Jefferies, and other banks are managing the offering. C4T focuses on targeted protein degradation therapies for cancer and other diseases.
C4 Therapeutics, Inc. (Nasdaq: CCCC) announced a proposed public offering of 4,250,000 shares of its common stock, with an option for underwriters to purchase an additional 637,500 shares. The net proceeds will support the company's research and clinical development activities. The offering is dependent on market conditions and has yet to be finalized. Lead managers include J.P. Morgan, Jefferies, Evercore ISI, BMO Capital Markets, and UBS Investment Bank. The registration statement has been filed with the SEC but is not yet effective.
C4 Therapeutics (Nasdaq: CCCC) has announced the successful dosing of the first patient in its clinical trial for CFT7455, an innovative MonoDAC™ treatment targeting IKZF1/3 for multiple myeloma and non-Hodgkin’s lymphomas. This significant milestone marks the company’s first program to advance to clinical trials. The Phase 1/2 trial will assess safety, tolerability, and anti-tumor activity in approximately 160 patients. Preliminary data from this trial is expected in 2022, reflecting C4T's commitment to improving cancer treatment outcomes.
C4 Therapeutics presented new pre-clinical data on CFT8919, a novel EGFR degrader, indicating significant tumor regression in models resistant to current EGFR inhibitors. The results suggest CFT8919 is effective against mutations like L858R, T790M, and C797S. Pre-clinical studies showed 85% degradation of mutant EGFR in tumors following treatment. The company plans to file an IND by mid-2022 and initiate a Phase 1 clinical trial by year-end 2022, aiming to address unmet needs in non-small cell lung cancer therapy.
C4 Therapeutics (Nasdaq: CCCC) announced the advancement of CFT8919, a selective BiDAC degrader targeting EGFR L858R, into IND-enabling studies. The company expects to file for an IND by mid-2022, aiming to initiate a Phase 1/2 trial by year-end 2022. Preclinical data highlighting CFT8919's potency and selective activity against NSCLC will be presented at the Keystone Symposium. The company continues to progress its other drug candidates and aims to have four in clinical trials by the end of 2022.
C4 Therapeutics (Nasdaq: CCCC) appointed Lauren White as chief financial officer effective June 21, 2021, succeeding Bill McKee, who will remain as a part-time consultant. White brings over 20 years of financial experience from Novartis, where she held senior roles including global head of business planning. C4T aims to advance its portfolio of targeted protein degraders and is preparing to initiate its first clinical trial. The leadership change is anticipated to strengthen financial strategies while enhancing the company's mission of transforming cancer treatment.
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