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Study details
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A Study of PF-08046054/SGN-PDL1V in Advanced Solid Tumors

Seagen, a wholly owned subsidiary of Pfizer
NCT IDNCT05208762ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

315

Study length

about 5.5 years

Ages

18+

Locations

25 sites in AL, CA, IA +5

What this study is about

Researchers are testing the safety of a drug called PF-08046054/SGN-PDL1V alone and with pembrolizumab in people with solid tumors. The trial will also trial the side effects of this drug.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take PF-08046054
  • 2.Take pembrolizumab

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

pembrolizumab (Immune checkpoint inhibitor; blocks PD-1 to boost T-cell attack on cancer)

Drug routes

infusion

Endpoints

Primary: Number of participants with adverse events (AEs), Number of participants with dose-limiting toxicities (DLTs), Number of participants with laboratory abnormalities

Secondary: Confirmed objective response rate (ORR) per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) by investigator assessment, Duration of objective response (DOR) per RECIST v1.1 by investigator assessment, Incidence of anti-drug antibodies (ADAs), Overall survival (OS), PK parameter - Maximum concentration (Cmax), PK parameter - Trough concentration (Ctrough), Pharmacokinetic (PK) parameter - Area under the concentration-time curve (AUC), Progression-free survival (PFS) per RECIST v1.1 by investigator assessment

Body systems

Oncology