C4 Therapeutics, Inc. (CCCC)
C4 Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on discovering and developing innovative therapeutic candidates. Its core strategy involves degrading proteins implicated in disease, addressing a range of conditions including cancer, neurodegenerative disorders, and other illnesses. The company's primary drug candidate, CFT7455, is an orally administered MonoDAC degrader of the IKZF1 and IKZF3 proteins. This compound is currently undergoing Phase 1/2 clinical trials for the treatment of multiple myeloma and various non-Hodgkin lymphomas, such as peripheral T-cell lymphoma and mantle cell lymphoma. Additionally, C4 Therapeutics is advancing several other programs: CFT8634, an orally bioavailable BiDAC degrader targeting the BRD9 protein, for potential use in synovial sarcoma and SMARCB1-deleted solid tumors. CFT1946, an orally administered BiDAC degrader designed to act on the V600X mutant BRAF, aimed at indications like melanoma, non-small cell lung cancer (NSCLC), colorectal cancer, and other solid malignancies. CFT8919, an orally available, allosteric, and mutant-selective BiDAC degrader specifically targeting epidermal growth factor receptor (EGFR) with an L858R mutation in NSCLC. Their early-stage pipeline also features RET degraders for various forms of cancer. C4 Therapeutics, Inc. has formed strategic partnerships with F. Hoffmann-La Roche Ltd and Hoffmann-La Roche Inc., Biogen MA, Inc., and Calico Life Sciences LLC. The company was established in 2015 and its headquarters are located in Watertown, Massachusetts.
Sector: Biological Products, (No Diagnostic Substances)
Industry: Biotechnology
C4 Therapeutics, Inc.
Trials need funding. See this company's dilution risk and cash position.
- Phase 2Recruiting
A Study to Evaluate the Efficacy of Cemsidomide + Dexamethasone in Participants With Relapsed/Refractory Multiple Myeloma
Cemsidomide, Dexamethasone
Multiple Myeloma, Relapsed/Refractory Multiple Myeloma
NCT07284758Enrollment100StartFeb 2026Primary CompletionMar 2030est.CompletionMar 2030est. - Phase 1Active, not recruiting
Study to Assess the Safety and Tolerability of CFT7455 in Relapsed/Refractory Non-Hodgkin's Lymphoma or Multiple Myeloma
cemsidomide, Dexamethasone Oral
Multiple Myeloma, Lymphoma, Non-Hodgkin's
NCT04756726Enrollment224StartApr 2021Primary CompletionSep 2026est.CompletionDec 2026est. - Phase 1Terminated
A Study to Assess the Safety and Tolerability of CFT8634 in Locally Advanced or Metastatic SMARCB1-Perturbed Cancers, Including Synovial Sarcoma and SMARCB1-Null Tumors
CFT8634
Synovial Sarcoma, Soft Tissue Sarcoma
NCT05355753Enrollment49StartMar 2022Primary CompletionDec 2023CompletionDec 2023 - Phase 1Completed
A Study to Characterize the Safety, Tolerability, and Preliminary Efficacy of CFT1946 as Monotherapy and Combination Therapy in Subjects With BRAF V600 Mutant Solid Tumors
CFT1946, Trametinib
Solid Tumors, Melanoma +3
NCT05668585Enrollment89StartDec 2022Primary CompletionNov 2025CompletionNov 2025 - Phase 1Recruiting
A Study to Learn About the Effects of Cemsidomide in Combination With Elranatamab in Relapsed/Refractory Multiple Myeloma Subjects
Cemsidomide, Elranatamab
Multiple Myeloma (MM)
NCT07280013Enrollment60StartFeb 2026Primary CompletionDec 2028est.CompletionJun 2029est.
| Drug / Therapy | Link | ||
|---|---|---|---|
| Phase 2 | Recruiting | Cemsidomide, Dexamethasone | NCT07284758 |
| Phase 1 | Active, not recruiting | cemsidomide, Dexamethasone Oral | NCT04756726 |
| Phase 1 | Terminated | CFT8634 | NCT05355753 |
| Phase 1 | Completed | CFT1946, Trametinib | NCT05668585 |
| Phase 1 | Recruiting | Cemsidomide, Elranatamab | NCT07280013 |