C4 Therapeutics Inc. (CCCC) – Company Press Releases
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C4 Therapeutics to Participate in the Stifel 2024 Targeted Oncology Forum
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C4 Therapeutics Presents New Preclinical Data for CFT1946 Highlighting Superior Activity as a Single Agent to Clinically Approved BRAF Inhibitor Standard of Care Combinations at the American Associati
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C4 Therapeutics to Present New Preclinical Data on Highly Selective Orally Bioavailable BiDAC™ Degraders at the American Association for Cancer Research Annual Meeting 2024
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C4 Therapeutics Announces Strategic Discovery Research Collaboration with Merck KGaA, Darmstadt, Germany, Against Critical Oncogenic Proteins
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C4 Therapeutics Reports Fourth Quarter and Full Year 2023 Financial Results and Recent Business Highlights
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C4 Therapeutics Announces 2024 Priorities and Extended Cash Runway to Advance Portfolio of Targeted Protein Degradation Medicines
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C4 Therapeutics Announces Closing of $25 Million Equity Investment by Betta Pharmaceuticals
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C4 Therapeutics to Present at the 42nd Annual J.P. Morgan Healthcare Conference
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C4 Therapeutics Announces Positive Data from CFT7455 Phase 1 Trial in Relapsed/Refractory Multiple Myeloma
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C4 Therapeutics Announces License and Research Collaboration with Merck to Discover and Develop Degrader-Antibody Conjugates (DACs)
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C4 Therapeutics to Host Webcast to Present New Dose Escalation Data from CFT7455 Phase 1 Study in Relapsed/Refractory Multiple Myeloma
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C4 Therapeutics Strengthens Board of Directors with Owen Hughes Appointment
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C4 Therapeutics Reports Third Quarter 2023 Financial Results and Recent Business Highlights
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C4 Therapeutics Announces Upcoming Data Presentations for CFT8634, an Orally Bioavailable BiDAC™ Degrader in Development for Synovial Sarcoma and SMARCB1-Null Tumors, and CFT7455, an Orally Bioavail
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C4 Therapeutics Announces Chief Financial Officer Succession
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C4 Therapeutics Reports Second Quarter 2023 Financial Results and Recent Business Highlights
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C4 Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
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C4 Therapeutics Announces FDA Clearance of Investigational New Drug Application for CFT8919, an Orally Bioavailable BiDAC™ Degrader Targeting EGFR L858R for Non-Small Cell Lung Cancer
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C4 Therapeutics Appoints Leonard Reyno, M.D., as Chief Medical Officer
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C4 Therapeutics and Betta Pharmaceuticals Announce Exclusive Licensing Agreement for the Development and Commercialization in Greater China of CFT8919, an Orally Bioavailable BiDAC™ Degrader of EGFR
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C4 Therapeutics Reports First Quarter 2023 Financial Results and Recent Business Highlights
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C4 Therapeutics to Participate in the Stifel 2023 Virtual Targeted Oncology Days
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C4 Therapeutics to Participate in the Stifel 2023 Virtual Targeted Oncology Days
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C4 Therapeutics Reports Fourth Quarter and Full Year 2022 Financial Results and Recent Business Highlights
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C4 Therapeutics Reports Fourth Quarter and Full Year 2022 Financial Results and Recent Business Highlights
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C4 Therapeutics to Present at Two Virtual February 2023 Conferences
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C4 Therapeutics to Present at Two Virtual February 2023 Conferences
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C4 Therapeutics Announces First Patient Dosed in Phase 1/2 Clinical Trial Evaluating CFT1946, an Orally Bioavailable BiDAC™ Degrader, in BRAF V600 Mutant Solid Tumors
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C4 Therapeutics Announces First Patient Dosed in Phase 1/2 Clinical Trial Evaluating CFT1946, an Orally Bioavailable BiDAC™ Degrader, in BRAF V600 Mutant Solid Tumors
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C4 Therapeutics Announces 2023 Strategic Priorities to Advance Portfolio of Targeted Protein Degradation Medicines
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C4 Therapeutics Announces 2023 Strategic Priorities to Advance Portfolio of Targeted Protein Degradation Medicines
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C4 Therapeutics to Present at the 41st Annual J.P. Morgan Healthcare Conference
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C4 Therapeutics to Present at the 41st Annual J.P. Morgan Healthcare Conference
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C4 Therapeutics Reports Third Quarter 2022 Financial Results and Recent Business Highlights
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C4 Therapeutics Reports Third Quarter 2022 Financial Results and Recent Business Highlights
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C4 Therapeutics Receives Study May Proceed Letter from U.S. FDA to Initiate Phase 1/2 Clinical Trial of CFT1946, an Orally Bioavailable BiDAC™ Degrader, in BRAF-V600 Mutant Solid Cancers
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C4 Therapeutics Receives Study May Proceed Letter from U.S. FDA to Initiate Phase 1/2 Clinical Trial of CFT1946, an Orally Bioavailable BiDAC™ Degrader, in BRAF-V600 Mutant Solid Cancers
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C4 Therapeutics to Present at Bank of America Securities Precision Oncology Conference 2022
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C4 Therapeutics to Present at Bank of America Securities Precision Oncology Conference 2022
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C4 Therapeutics Reports Second Quarter 2022 Financial Results and Recent Business Highlights
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C4 Therapeutics Reports Second Quarter 2022 Financial Results and Recent Business Highlights
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C4 Therapeutics Appoints Experienced Clinical Development Leaders Laura Bessen, M.D. and Donna Grogan, M.D. to Board of Directors
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C4 Therapeutics Appoints Experienced Clinical Development Leaders Laura Bessen, M.D. and Donna Grogan, M.D. to Board of Directors
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C4 Therapeutics Announces First Patient Dosed in Phase 1/2 Clinical Trial Evaluating CFT8634, an Orally Bioavailable BiDAC™ Degrader for the Treatment of Synovial Sarcoma and SMARCB1-null Tumors
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C4 Therapeutics Announces First Patient Dosed in Phase 1/2 Clinical Trial Evaluating CFT8634, an Orally Bioavailable BiDAC™ Degrader for the Treatment of Synovial Sarcoma and SMARCB1-null Tumors
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C4 Therapeutics Reports First Quarter 2022 Financial Results and Recent Business Highlights
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C4 Therapeutics Reports First Quarter 2022 Financial Results and Recent Business Highlights
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C4 Therapeutics Presents Clinical Data from Cohort A of the Ongoing Phase 1/2 Clinical Trial of CFT7455, a Novel IKZF1/3 Degrader
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C4 Therapeutics Presents Clinical Data from Cohort A of the Ongoing Phase 1/2 Clinical Trial of CFT7455, a Novel IKZF1/3 Degrader
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C4 Therapeutics Appoints Utpal Koppikar to Board of Directors
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