Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Active, not recruiting Phase 1 Interventional

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

ClinicalTrials.gov ID: NCT05355701

Public ClinicalTrials.gov record NCT05355701. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 3:04 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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 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 or cetuximab and mFOLFOX6 (Chemotherapy regimen). 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.

Study identification

NCT ID
NCT05355701
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
Pfizer
Industry
Enrollment
103 participants

Conditions and interventions

Eligibility (public fields only)

Age range
16 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 4, 2022
Primary completion
Aug 30, 2027
Completion
Aug 30, 2027
Last update posted
Aug 31, 2026

2022 – 2027

United States locations

U.S. sites
31
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
Highlands Oncology Group, PA Fayetteville Arkansas 72703
Highlands Oncology Group, PA Rogers Arkansas 72758
Highlands Oncology Group, PA Springdale Arkansas 72762
Clinical and Translational Research Center (CTRC) Aurora Colorado 80045
UCHealth Sue Anschutz-Rodgers Eye Center Aurora Colorado 80045
University of Colorado Hospital - Anschutz Cancer Pavilion (ACP) Aurora Colorado 80045
University of Colorado Hospital - Anschutz Inpatient Pavilion (AIP) Aurora Colorado 80045
University of Colorado Hospital - Anschutz Outpatient Pavilion (AOP) Aurora Colorado 80045
Sylvester Comprehensive Cancer Center Miami Florida 33136
University of Miami Hospital and Clinics Miami Florida 33136
Brigham and Women's Hospital Boston Massachusetts 02115
Dana-Farber Cancer Institute Boston Massachusetts 02215
Dana-Farber Cancer Institute - Chestnut Hill Newton Massachusetts 02467
Brigitte Harris Cancer Pavilion Detroit Michigan 48202
Henry Ford Cancer - Detroit (Brigitte Harris Cancer Pavilion) Detroit Michigan 48202
Henry Ford Medical Center - Columbus Novi Michigan 48377
CT Scan and Echo Only: Henry Ford Medical Center-Plymouth Plymouth Michigan 48170
MSK Monmouth Middletown New Jersey 07748
MSK David H. Koch Center for Cancer Care New York New York 10021
Memorial Sloan Kettering Cancer Center 53rd street New York New York 10022
Memorial Sloan Kettering Cancer Center New York New York 10065
Cleveland Clinic Taussig Cancer Center Investigational Pharmacy Cleveland Ohio 44106
Cleveland Clinic Cleveland Ohio 44195
Providence Cancer Institute Franz Clinic Portland Oregon 97213
Providence Portland Medical Center Portland Oregon 97213
Sarah Cannon Research Institute - Pharmacy Nashville Tennessee 37203
SCRI Oncology Partners Nashville Tennessee 37203
TriStar Bone Marrow Transplant Nashville Tennessee 37203
TriStar Centennial Medical Center - Cell Processing Lab Nashville Tennessee 37203
TriStar Centennial Medical center Nashville Tennessee 37203
START San Antonio San Antonio Texas 78229

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05355701, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 31, 2026 · Synced Sep 2, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05355701 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →