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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. logo

C4 Therapeutics, Inc.

NASDAQ:CCCCHealthcare
+2.12%$3.37
AH$3.28-2.77%vs close
Mkt Cap$414.59M
Float98.54M
O/S123.03M
Vol
$ Vol
RVOL
Inst Own96.4%
SI43.4%
Earnings
Dilution
Phase Distribution
5 lead-sponsored trials·3 active·1 completed
Phase 14
Phase 21
Status Overview
Recruiting2
Active, not recruiting1
Completed1
Stopped1

Trials need funding. See this company's dilution risk and cash position.

Clinical Trials
Status
Phase
  • Phase 2
    Recruiting

    A Study to Evaluate the Efficacy of Cemsidomide + Dexamethasone in Participants With Relapsed/Refractory Multiple Myeloma

    Cemsidomide, Dexamethasone

    Multiple Myeloma, Relapsed/Refractory Multiple Myeloma

    Enrollment
    100
    Start
    Feb 2026
    Primary Completion
    Mar 2030est.
    Completion
    Mar 2030est.
    NCT07284758
  • Phase 1
    Active, 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

    Enrollment
    224
    Start
    Apr 2021
    Primary Completion
    Sep 2026est.
    Completion
    Dec 2026est.
    NCT04756726
  • Phase 1
    Terminated

    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

    Enrollment
    49
    Start
    Mar 2022
    Primary Completion
    Dec 2023
    Completion
    Dec 2023
    NCT05355753
  • Phase 1
    Completed

    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

    Enrollment
    89
    Start
    Dec 2022
    Primary Completion
    Nov 2025
    Completion
    Nov 2025
    NCT05668585
  • Phase 1
    Recruiting

    A Study to Learn About the Effects of Cemsidomide in Combination With Elranatamab in Relapsed/Refractory Multiple Myeloma Subjects

    Cemsidomide, Elranatamab

    Multiple Myeloma (MM)

    Enrollment
    60
    Start
    Feb 2026
    Primary Completion
    Dec 2028est.
    Completion
    Jun 2029est.
    NCT07280013