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Study identifier: NCT05918445 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

PM8002 in the Treatment of Patients With Advanced Solid Tumors

Condition: Malignant Neoplasm  ·  Sponsor: Biotheus Inc.

PhasePhase 1/Phase 2
Planned participants380
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This study is to characterize the safety, tolerability, pharmacokinetics (PK), immunogenicity, pharmacodynamics (PD) and anti-tumor activity of PM8002, a PD-L1/VEGF bispecific antibody, as a single agent in adult subjects with advanced solid tumors.

This description comes directly from the study's public registry record.

Talk to the study team

Ye Guo  ·  135 0167 8472  ·  pattrickguo@gmail.com

Always discuss trial participation with your own doctor first.

Locations (48)

Baoji Central HospitalBaoji, ChinaRecruiting
Baoji Central HospitalBaoji, ChinaRecruiting
Cancer Hospital Chinese Academy of Medical SciencesBeijing, ChinaRecruiting
Peking University Cancer HospitalBeijing, ChinaRecruiting
Peking University Cancer HospitalBeijing, ChinaRecruiting
Jilin Cancer HospitalChangchun, ChinaRecruiting
The First Hospital of Jilin UniversityChangchun, ChinaRecruiting
Changde First People's HospitalChangde, ChinaRecruiting
Hunan Provincial People's HospitalChangsha, ChinaRecruiting
The First People's Hospital of ChangzhouChangzhou, ChinaRecruiting
Chengdu Integrated TCM& Western Medicine HospitalChengdu, ChinaRecruiting
Sichuan Cancer HospitalChengdu, ChinaRecruiting

+ 36 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05918445