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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Seagen Pfizer CT.gov Call Center 1-800-718-1021
ClinicalTrials.gov_Inquiries@pfizer.com


Study Location:

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Be Part of Research - Trial Details - A Study of SGN-PDL1V in Advanced Solid Tumors

A Study of SGN-PDL1V in Advanced Solid Tumors

Recruiting

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Carcinoma
Neoplasms
Carcinoma, Squamous Cell
Stomach Neoplasms
Breast Neoplasms
Esophageal Squamous Cell Carcinoma
Carcinoma, Non-Small-Cell Lung
Squamous Cell Carcinoma of Head and Neck
Ovarian Neoplasms
Triple Negative Breast Neoplasms


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 study will test the safety of a drug called PF-08046054/SGN-PDL1V alone and with pembrolizumab in participants with solid tumors. It will also study the side effects of this drug. A side effect is anything a drug does to your body besides treating your disease.

Participants will have solid tumor cancer that has spread through the body (metastatic) or cannot be removed with surgery (unresectable).

This study will have five parts. Parts A and B of the study will find out how much PF-08046054/SGN- PDL1V should be given to participants. Part C will use the dose found in Parts A and B to find out how safe PF-08046054/SGN-PDL1V is and if it works to treat solid tumor cancers. In Part D and E, participants will be given PF-08046054/SGN-PDL1V with pembrolizumab to find out how safe this combination is and if it works to treat solid tumor cancers.

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:

Oct 2022 Nov 2027

INTERVENTIONAL

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

Intervention Arm Group : PF-08046054 Combination Therapy;PF-08046054 Monotherapy;

Intervention Type : DRUG
Intervention Description : 200 mg once every 3 weeks given into the vein (IV; intravenously)

Intervention Arm Group : PF-08046054 Combination Therapy;



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.

  • Royal Marsden Hospital
    Sutton
    Surrey
    SM2 5PT
  • Sarah Cannon Research Institute
    London
    W1G 6AD
  • Diagnostic Centre
    London
    Others
    WlG 7AF
  • The Harley Street Clinic (THSC)
    London
    Other
    W1G 8BJ
  • Pharmacy: Royal Marsden Hospital
    Sutton
    Surrey
    SM2 5PT
  • Radiology
    London
    W1G 8PP

Seagen Pfizer CT.gov Call Center 1-800-718-1021
ClinicalTrials.gov_Inquiries@pfizer.com



The study is sponsored by Seagen Inc.




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Read full details for Trial ID: NCT05208762
Last updated 15 April 2025

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