A Study of SGN-CEACAM5C in Adults With Advanced Solid Tumors

⚠️

This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

This clinical trial is studying advanced solid tumors. Solid tumors are cancers that start in a part of your body like your lungs or liver instead of your blood. Once tumors have grown bigger in one place but haven't spread, they're called locally advanced. If your cancer has spread to other parts of your body, it's called metastatic. When a cancer has gotten so big it can't easily be removed or has spread to other parts of the body, it is called unresectable. These types of cancer are harder to treat. Participants in this study must have cancer that has come back or did not get better with treatment. Participants must have a solid tumor cancer that can't be treated with standard of care drugs. This clinical trial uses an experimental drug called PF-08046050. PF-08046050 is a type of antibody-drug conjugate or ADC. ADCs are designed to stick to cancer cells and kill them. They may also stick to some normal cells. This study will test the safety of PF-08046050 in participants with solid tumors that are hard to treat or have spread throughout the body. This study has 5 different study parts. Part A and Part B of the study will find out how much PF-08046050 should be given to participants. Part C will use the information from Parts A and B to see if PF-08046050 is safe and if it works to treat certain solid tumor cancers. Part D and E of the study, together with information from Parts A and B, will find out how much PF-08046050 should be given in combination with other anti-cancer agents. Part E will use the information from Parts A, B, and D to see if PF-08046050 is safe in combination with other anti-cancer agents and if it works to treat a certain solid tumor.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • Pacjent ma zaawansowanego litego raka (np. płuca, jelita, żołądka, trzustki), który nie jest łatwy do usunięcia chirurgicznie lub rozprzestrzenił się w organizmie.
  • Rak u pacjenta powrócił lub nie poprawił się po wcześniejszym leczeniu.
  • Rak pacjenta nie reaguje na standardowe leki lub nie ma dla niego odpowiedniego standardowego leczenia.
  • Rak pacjenta musiał być potwierdzony badaniami laboratoryjnymi (nie wystarczy tylko stwierdzenie obecności guza).
  • W niektórych częściach badania pacjent musiał przejść ograniczoną liczbę wcześniejszych linii leczenia.

✗ Disqualifies

  • Pacjent ma nowotwór, który nie jest rakiem litym (np. białaczkę).
  • Pacjent ma guzy, które są łatwe do usunięcia chirurgicznie.
  • Rak pacjenta nie rozprzestrzenił się w organizmie i można go łatwo usunąć.
  • Pacjent miał bardzo wiele wcześniejszych prób leczenia nowotworu, które mogłyby wpłynąć na działanie badanego leku.

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
July 22, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (48)

Mayo Clinic Hospital

Phoenix, United States

Mayo Clinic

Scottsdale, United States

City of Hope (City of Hope National Medical Center, City of Hope Medical Center)

Duarte, United States

IP Address: City of Hope Investigational Drug Services(IDS)

Duarte, United States

University of Colorado Hospital - Anschutz Cancer Pavilion (ACP)

Aurora, United States

University of Colorado Hospital

Aurora, United States

Florida Cancer Specialists

Orlando, United States

Sarah Cannon Research Institute at Florida Cancer Specialists

Orlando, United States

Sidney Kimmel Comprehensive Cancer at Johns Hopkins

Baltimore, United States

Beth Israel Deaconess Medical Center

Boston, United States

START Midwest

Grand Rapids, United States

Mayo Clinic Cancer Center

Rochester, United States

Mayo Clinic

Rochester, United States

MidAmerica Cancer Care

Kansas City, United States

Sarah Cannon Research Institute - Pharmacy

Nashville, United States

SCRI Oncology Partners

Nashville, United States

The University of Texas MD Anderson Cancer Center

Houston, United States

NEXT Dallas

Irving, United States

South Texas Accelerated Research Therapeutics, LLC

San Antonio, United States

START Mountain Region

Salt Lake City, United States

South Texas Accelerated Research Therapeutics Mountain Region

West Valley City, United States

The Ottawa Hospital

Ottawa, Canada

University Health Network

Toronto, Canada

University Health Network, Princess Margaret Cancer Centre

Toronto, Canada

McGill University Health Centre

Montreal, Canada

The Sixth Affiliated Hospital of Sun Yat-sen University

Guangzhou, China

Shandong First Medical University Cancer Hospital

Jinan, China

Fudan University Shanghai Cancer Center

Shanghai, China

Institut Gustave Roussy

Villejuif, France

Gustave Roussy

Villejuif, France

Hadassah Medical Organization

Jerusalem, Israel

National Cancer Center Hospital East

Kashiwa, Japan

Netherlands Cancer Institute

Amsterdam, Netherlands

Institut Catala d'Oncologia - Hospital Duran i Reynals (ICO L'Hospitalet)

L'Hospitalet de Llobregat, Spain

Ascires Cetir

Barcelona, Spain

Ascires CETIR

Esplugues de Llobregat, Spain

Servicio de Farmacia ICO - Planta 0

L'Hospitalet de Llobregat, Spain

Hospital Universitario HM Sanchinarro-CIOCC-START Madrid

Madrid, Spain

Karolinska University Hospital

Solna, Sweden

ApoEx NKS

Stockholm, Sweden

The Harley Street Clinic (THSC)

London, United Kingdom

Edinburgh Cancer Centre, Western General Hospital

Edinburgh, United Kingdom

Lothian Health Board

Edinburgh, United Kingdom

Western General Hospital

Edinburgh, United Kingdom

Sarah Cannon Research Institute UK

London, United Kingdom

Diagnostic Centre

London, United Kingdom

The Harley Street Clinic

London, United Kingdom

Radiology

London, United Kingdom

Trial contact

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/7/2026.

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