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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

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT06799533. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 13, 2026, 5:09 PM EST

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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
May 1, 2025 (Actual)
Primary completion
Feb 23, 2026 (Actual)
Completion
Feb 23, 2026 (Actual)
Last update posted
Mar 18, 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 18, 2026 · Synced Nov 13, 2026

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