A Study of PF-08046052/SGN-EGFRd2 in Advanced Solid Tumors
NCT05983133 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 68
Last updated 2026-05-05
Summary
This study will test the safety of a drug called PF-08046052/SGN-EGFRd2 in participants with advanced solid tumors. 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.
Participants will have cancer that cannot be removed (unresectable) or has spread through the body (metastatic).
This study will have three parts. Parts A and B of the study will find out how much PF-08046052/SGN-EGFRd2 should be given to participants. Part C will use the dose found in parts A and B to find out how safe PF-08046052/SGN-EGFRd2 is and if it works to treat solid tumor cancers.
Conditions
- Colorectal Neoplasms
- Carcinoma, Non-Small-Cell Lung
- Squamous Cell Carcinoma of the Head and Neck
- Pancreatic Ductal Adenocarcinoma
Interventions
- DRUG
-
PF-08046052
Given into the vein (IV; intravenously)
Sponsors & Collaborators
-
Seagen, a wholly owned subsidiary of Pfizer
lead INDUSTRY
Principal Investigators
-
Pfizer CT.gov Call Center · Pfizer
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-11-14
- Primary Completion
- 2026-04-16
- Completion
- 2026-04-16
- FDA Drug
- Yes
Countries
- United States
- United Kingdom
Study Locations
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