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A Study of PF-08046052/SGN-EGFRd2 in Advanced Solid Tumors
NCT05983133 · View on ClinicalTrials.gov ↗
Study 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 Studied
Interventions
- DRUG PF-08046052
Study Locations (20)
California
- Ronald Reagan UCLA Medical Center — Los Angeles
- UCLA Hematology/Oncology — Los Angeles
- Santa Monica UCLA Medical Center & Orthopaedic Hospital — Santa Monica
- UCLA Hematology/Oncology - Santa Monica — Santa Monica
Florida
- Moffitt Cancer Center McKinley Hospital — Tampa
- Moffitt Cancer Center — Tampa
Michigan
- Karmanos Cancer Institute — Detroit
- Karmanos Cancer Institute Weisberg Cancer Treatment Center — Farmington Hills
New Jersey
- Hackensack University Medical Center — Hackensack
- John Theurer Cancer Center at Hackensack University Medical Center — Hackensack
North Carolina
- Atrium Health Wake forest Baptist — Winston-Salem
- Wake Forest Baptist Medical Center / Wake Forest University — Winston-Salem
Oregon
- Providence Cancer Institute Franz Clinic — Portland
- Providence Portland Medical Center — Portland
Texas
- MD Anderson Cancer Center - University of Texas — Houston
- The University of Texas MD Anderson Cancer Center — Houston
Iowa
- University of Iowa — Iowa City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 65 participants |
| Start Date | 2023-11-14 |
| Est. Completion | 2026-08-14 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05983133
The ClinicalTrials.gov registry entry for NCT05983133 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 65 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Seagen, a wholly owned subsidiary of Pfizer, which has 51 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 4 conditions, with Carcinoma, Non-Small-Cell Lung appearing as the primary indexed condition, and to 1 intervention — of which PF-08046052 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05983133 reports 20 study locations spanning 11 distinct geographic areas — top geographies include California, Florida, Michigan. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05983133 about?
NCT05983133 is a clinical study titled "A Study of PF-08046052/SGN-EGFRd2 in Advanced Solid Tumors". 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 ...
What is the current status of trial NCT05983133?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 65 participants. The study started on 2023-11-14. Estimated completion is 2026-08-14.
What conditions does trial NCT05983133 study?
This clinical trial studies the following conditions: Carcinoma, Non-Small-Cell Lung, Pancreatic Ductal Adenocarcinoma, Colorectal Neoplasms, Squamous Cell Carcinoma of the Head and Neck. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05983133?
The interventions under investigation include: PF-08046052 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05983133?
This trial is sponsored by Seagen, a wholly owned subsidiary of Pfizer, which has 51 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05983133 being conducted?
This trial has 20 study locations across California, Florida, Iowa, Massachusetts, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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