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Contact Information:

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Be Part of Research - Trial Details - A Study of SGN-CEACAM5C in Adults With Advanced Solid Tumors

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

Recruiting

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Carcinoma
Neoplasms
Adenocarcinoma
Colorectal Neoplasms
Carcinoma, Non-Small-Cell Lung
Stomach Neoplasms
Small Cell Lung Carcinoma


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


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 of the study, together with information from Parts A and B, will find out how much PF-08046050 should be given to participants in combination with bevacizumab. Part E will use the information from Parts A, B, and D to see if PF-08046050 is safe in combination with bevacizumab and if it works to treat a certain solid tumor.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Nov 2023 Nov 2029

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : Given into the vein (IV; intravenous)

Intervention Arm Group : PF-08046050;PF-08046050 +bevacizumab;

Intervention Type : DRUG
Intervention Description : Given into the vein (IV; intravenous)

Intervention Arm Group : PF-08046050 +bevacizumab;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Sarah Cannon Research Institute UK
    London
    W1G 6AD
  • The University of Edinburgh
    Edinburgh
    EH4 2XU


The study is sponsored by Seagen, a wholly owned subsidiary of Pfizer and is in collaboration with Sanofi.




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Read full details for Trial ID: NCT06131840
Last updated 17 July 2025

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