A Study to Learn About the Study Medicine Called PF-07799933 in People With Advanced Solid Tumors With BRAF Alterations.

Description

The purpose of this clinical trial is to learn about the safety and effects of the study medicine (called PF-07799933) administered as a single agent and in combination with other study medicines (called binimetinib) in people with solid tumors. This study is seeking participants who have an advanced solid tumor with a certain type of abnormal gene called "BRAF" and available treatments are no longer effective in controlling their cancer. All participants in this study will receive PF-07799933. PF-07799933 comes as a tablet to take by mouth, 2 times a day. Depending on the part of the study, participants may also receive another study medicine: * People with melanoma or other solid tumors may also receive binimetinib. Binimetinib comes as a tablet to take by mouth, 2 times a day. * People with colorectal cancer may also receive cetuximab. Cetuximab will be given weekly (or every two weeks) in the clinic as a shot given in the vein or port (intravenous, IV). Participants may receive the study medicines for about 2 years. The study team will monitor how each participant is doing with the study treatment during regular visits at the study clinic.

Conditions

Melanoma, Non-Small-Cell Lung Cancer, Thyroid Cancer, Glioma

Study Overview

Study Details

Study overview

The purpose of this clinical trial is to learn about the safety and effects of the study medicine (called PF-07799933) administered as a single agent and in combination with other study medicines (called binimetinib) in people with solid tumors. This study is seeking participants who have an advanced solid tumor with a certain type of abnormal gene called "BRAF" and available treatments are no longer effective in controlling their cancer. All participants in this study will receive PF-07799933. PF-07799933 comes as a tablet to take by mouth, 2 times a day. Depending on the part of the study, participants may also receive another study medicine: * People with melanoma or other solid tumors may also receive binimetinib. Binimetinib comes as a tablet to take by mouth, 2 times a day. * People with colorectal cancer may also receive cetuximab. Cetuximab will be given weekly (or every two weeks) in the clinic as a shot given in the vein or port (intravenous, IV). Participants may receive the study medicines for about 2 years. The study team will monitor how each participant is doing with the study treatment during regular visits at the study clinic.

A PHASE 1, OPEN-LABEL, DOSE ESCALATION AND DOSE EXPANSION STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS, AND ANTI TUMOR ACTIVITY OF PF-07799933 (ARRY-440) AS A SINGLE AGENT AND IN COMBINATION THERAPY IN PARTICIPANTS 16 YEARS AND OLDER WITH ADVANCED SOLID TUMORS WITH BRAF ALTERATIONS

A Study to Learn About the Study Medicine Called PF-07799933 in People With Advanced Solid Tumors With BRAF Alterations.

Condition
Melanoma
Intervention / Treatment

-

Contacts and Locations

Fayetteville

Highlands Oncology Group, Fayetteville, Arkansas, United States, 72703

Rogers

Highlands Oncology Group, Rogers, Arkansas, United States, 72758

Springdale

Highlands Oncology Group, Springdale, Arkansas, United States, 72762

Aurora

Clinical and Translational Research Center (CTRC), Aurora, Colorado, United States, 80045

Aurora

Clinical And Translational Research Center, Aurora, Colorado, United States, 80045

Aurora

UCHealth Sue Anschutz-Rodgers Eye Center, Aurora, Colorado, United States, 80045

Aurora

University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States, 80045

Aurora

University of Colorado Hospital - Anschutz Cancer Pavilion (ACP), Aurora, Colorado, United States, 80045

Aurora

University of Colorado Hospital - Anschutz Inpatient Pavilion (AIP), Aurora, Colorado, United States, 80045

Aurora

University of Colorado Hospital - Anschutz Outpatient Pavilion (AOP), Aurora, Colorado, United States, 80045

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Diagnosis of advanced/metastatic solid tumor including primary brain tumor.
  • * Qualifying BRAF alteration (V600 or non-V600 Class II/Class III BRAF alteration), in tumor tissue and/or blood (ie circulating tumor deoxyribonucleic acid \[DNA\], or ctDNA).
  • * Disease progressed during/following last prior treatment and no satisfactory alternative treatment options (Part 1 and Part 2).
  • * Tumor specific cohorts (melanoma, colorectal cancer) must have received specific prior approved therapies
  • * Brain metastasis larger than 4 cm
  • * Systemic anti-cancer therapy or small molecule therapeutics ongoing at the start of study treatment.
  • * For participants who may get binimetinib on study, history or current evidence of retinal vein occlusion (RVO) or concurrent neuromuscular disorder associated with elevated creatine kinase (CK)

Ages Eligible for Study

16 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Pfizer,

Pfizer CT.gov Call Center, STUDY_DIRECTOR, Pfizer

Study Record Dates

2027-12-26