A Study to Characterize the Safety, Tolerability, and Preliminary Efficacy of CFT1946 as Monotherapy and in Combination With Trametinib in Subjects With BRAF V600 Mutant Solid Tumors

• Status: Recruiting
• Trial end date: 2027-04-11
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to evaluate the safety and tolerability of CFT1946 as well as to determine the maximum tolerated dose (MTD) and/or the recommended Phase 2 dose (RP2D) of CFT1946 as monotherapy (Arm A) and in combination with trametinib (CFT1946 + trametinib; Arm B).

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: C4 Therapeutics, Inc.
• Treatments: Trametinib

Criteria

Inclusion Criteria:

1. Subject (or legal guardian, where applicable) is willing and able to provide signed informed consent and can follow protocol requirements

2. Subject is ≥18 years of age at time of informed consent

3. Eastern Cooperative Oncology Group performance status of 0 or 1

4. Subject has documented evidence of a BRAF V600 mutation obtained from tumor tissue or liquid biopsy: (other protocol conditions may apply)

5. Subject must have received ≥1 prior line of SoC therapy for their locally advanced or metastatic disease, NSCLC, CRC, ATC or other BRAF-V600 mutation positive tumors:

1. Melanoma or NSCLC (Phase 1 and Phase 2 Arms A1 and B1): Prior receipt of a BRAF inhibitor and an immune checkpoint inhibitor (any sequence or combination). Prior (neo)adjuvant immunotherapy may be acceptable.

2. NSCLC (Phase 2 Arm B2): Prior receipt of a regimen including an immune checkpoint inhibitor (any sequence or combination). BRAF inhibitor naïve. Prior (neo)adjuvant immunotherapy may be acceptable.

3. CRC: Receipt of a SoC chemotherapy regimen and a prior BRAF inhibitor in combination with an EGFR monoclonal antibody. Subjects with documented MSI-H or dMMR CRC must have received prior immunotherapy. Subjects with MSS disease must have received at least 2 prior treatments. Subjects who received neo(adjuvant) chemotherapy regimens may be eligible.

4. ATC: Subjects must have received SoC therapy options including BRAF inhibitor if available and of benefit to the subject

5. Other BRAF V600 mutant solid tumors (non-CNS): Subjects must have received SoC therapy options per their Investigator's best judgment and be BRAF inhibitor naïve

6. Subject has measurable disease per RECIST v1.1

7. Adequate bone marrow, liver, renal, and cardiac organ function

8. A female subject may be eligible if not pregnant, planning a pregnancy, not breast feeding, a women of non-child bearing potential or a WOCBP willing to comply with protocol conditions relating to the use contraception, ova or blood donation and pregnancy testing prior to the first dose

9. A male subject must agree to comply with protocol conditions relating to the use of contraception, sperm and blood donation

10. Subject can safely swallow a tablet or pill

Other protocol defined exclusion criteria may apply

Exclusion Criteria:

1. Subject has had major surgery within 21 days prior to the planned first dose. Minor surgery is permitted within 21 days prior to enrollment

2. Subject with CNS involvement (primary tumor or metastatic disease), except if clinically stable, have no evidence of new or enlarging brain metastases and are on stable or tapering doses of steroids for at least 7 days prior to first dose. Subjects with untreated brain metastases may be eligible to enter without prior radiation therapy.

3. Subject with known malignancy other than trial indication that is progressing or has required treatment within the past 3 years, except for conditions that have undergone potentially curative therapy

4. Subject with history of thromboembolic or cerebrovascular events ≤6 months as defined in the protocol

5. Subject with impaired cardiac function or clinically significant cardiac disease, as defined in the protocol

6. Subject with history of uncontrolled diabetes mellitus (only for subjects who will receive CFT1946 + trametinib)

7. Subject with history or current evidence of retinal vein occlusion (RVO), chorioretinopathy, or current risk factors for RVO (only for subjects who will receive CFT1946 + trametinib)

8. Subject has received live, attenuated vaccine within 28 days prior to first dose administration

9. Subject has history of pneumonitis or interstitial lung disease

10. Subject has history of uveitis

11. Subject has known human immunodeficiency virus (HIV) infection (with exceptions)

12. Subject has history of or known HBV or active HCV infection

13. Subject has concurrent administration of strong CYP3A4/5 inhibitors and inducers, including any herbal medications/supplements

14. Subject has presence of Grade ≥2 toxicity due to prior cancer therapy, excepting alopecia and hypothyroidism requiring thyroid replacement therapy

15. Subject has initiation or receipt of the following ≤7 days prior to first dose administration: Hematopoietic colony-stimulating growth factors, transfusion of packed red blood cells (pRBC), and transfusion of platelets

16. Subject is pregnant, breastfeeding, or expecting to conceive or father children any time during the study

Other protocol defined exclusion criteria may apply