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Study identifier: NCT06346041 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Safety and Efficacy of Intravenous IDOV-SAFETM in Patients With Advanced Solid Tumors

Condition: Neoplasms  ·  Sponsor: Cancer Institute and Hospital, Chinese Academy of Medical Sciences

PhaseEARLY_Phase 1
Planned participants19
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This is an open-label, dose escalation, phase I study to evaluate safety tolerability, MTD or MFD, pharmacokinetic profile, immunogenicity, and pharmacodynamic profile of IDOV-SAFETM in patients with advanced solid tumors.

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

Talk to the study team

Ning Li, MD  ·  15601395554  ·  lining@cicams.ac.cn

Shuhang Wang, PhD  ·  13581809307  ·  wangshuhang@cicams.ac.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Cancer Hospital, Chinese Academy of Medical SciencesBeijing, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06346041