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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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take PF-08046054
  • 2.Take pembrolizumab
PhasePhase 1
Drugpembrolizumab
Routeinfusion
Primary goalNumber of participants with adverse events (AEs)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low8%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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