CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 116 target
Drug / intervention
pembrolizumab, pazopanibdrug
Likely dose
Not stated in record
Key inclusion· 9
  • Histologically confirmed soft tissue sarcoma with progression to 1 or 2 prior chemotherapy regimens
  • Age greater than 19 and not exceeding 80 years at study entry
  • ECOG performance status 0 or 1
  • Measurable disease by RECIST v1.1
Key exclusion· 21
  • Excluded sarcoma subtypes: embryonal rhabdomyosarcoma, chondrosarcoma, osteosarcoma, Ewing tumors, primitive neuroectodermal tumor, gastrointestinal stromal tumor, dermatofibrosarcoma protuberans, inflammatory myofibroblastic sarcoma, liposarcoma
  • Prior treatment with PD-1, PD-L1, anti-PD-L2, CTLA-4, OX-40, CD137 inhibitors, or pazopanib
  • Unresolved toxicity NCI CTCAE Grade ≥2 from prior anticancer therapy
  • Major surgical procedure within 28 days before first dose

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05679921
NCT05679921Phase 2RecruitingOn TrackUpdated 11mo ago

Pazopanib With or Without Pembrolizumab for Metastatic Soft Tissue Sarcoma: Open-label, Multicenter, Randomized, Phase 2 Trials

Yonsei University·interventional·Posted Jan 11, 2023·Updated Jul 16, 2025

In Brief

A Phase 2 clinical trial evaluating pembrolizumab, pazopanib for Soft Tissue Sarcoma. Currently recruiting, targeting 116 participants across 1 site.

Detailed Summary

This is an open-label, randomized, phase II study to evaluate the clinical activity of pembrolizumab in combination with pazopanib compared to pazopanib monotherapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesSouth Korea
Collaborators--

Timeline

Phase 2Recruiting
20232024202520262027
First PostedJan 11, 2023
Enrollment StartMar 1, 2024
Primary CompletionDec 31, 2026
TodayJul 2, 2026
Enrollment to primary: 2.8 yearsPosted 3.5 years agoPrimary completion in 6 months

Interventions

pembrolizumab, pazopanibdrug

Pembrolizumab will be given for a maximum of 2 years i.e. a total of 35 cycles of pembrolizumab with the q3 week dosing. Participants who complete study intervention after 2 years of pembrolizumab can be treated with pazopanib monotherapy based on physician's judgement. The duration of optional pembrolizumab crossover treatment will be maximum of 2 years i.e. a total of 35 cycles of pembrolizumab for patients progressing on pazopanib.