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Terminated Phase 1 Interventional

A Study to Learn About the Study Medicine Called PF-08046031 in Advanced Melanoma and Other Solid Tumors

ClinicalTrials.gov ID: NCT06799533

Public ClinicalTrials.gov record NCT06799533. 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 24, 2026, 2:01 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

AN OPEN-LABEL PHASE 1 STUDY TO INVESTIGATE PF-08046031 IN ADULTS WITH ADVANCED MELANOMA AND OTHER SOLID TUMORS

Brief summary

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

This study will test the safety of a drug called PF-08046031 in participants with melanoma and other solid tumors that have no current approved treatment or have spread through the body. It will also study the side effects of this drug. A side effect is anything a drug does to the body besides treating the disease. The study will have 3 parts. Part A and B of the study will find out how much PF-08046031 should be given to participants. Part C will use the information from Parts A and B to see if PF-08046031 is safe and if it works to treat solid tumor cancers.

Study identification

NCT ID
NCT06799533
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Pfizer
Industry
Enrollment
11 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Apr 30, 2025
Primary completion
Feb 22, 2026
Completion
Feb 22, 2026
Last update posted
Mar 17, 2026

2025 – 2026

United States locations

U.S. sites
7
U.S. states
2
U.S. cities
4
Facility City State ZIP Site status
The Angeles Clinic and Research Institue, A Cedars-Sinai Affiliate Los Angeles California 90025
The Angeles Clinic And Research Institute, A Cedars-Sinai Affiliate Los Angeles California 90025
UCSF Helen Diller Family Comprehensive Cancer Center San Francisco California 94143
UCSF Medical Center, Investigational Pharmacy San Francisco California 94158
The Angeles Clinic and Research Institue, A Cedars-Sinai Affiliate (Emergency Back-up only) Santa Monica California 90404
Presbyterian/ St. Lukes Medical Center Denver Colorado 80218
Sarah Cannon Research Institute at HealthONE - SCRI - PPDS Denver Colorado 80218

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06799533, 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 Mar 17, 2026 · Synced Sep 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06799533 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →