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Study identifier: NCT06234397 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Dose Escalation and Expansion Study of BH3120 Alone or With Pembrolizuamb in Advanced or Metastatic Solid Tumors

Condition: Advanced or Metastatic Solid Tumors  ·  Sponsor: Hanmi Pharmaceutical Company Limited

PhasePhase 1
Planned participants245
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a First-in-Human, Phase 1, Dose-Escalation and Dose-Expansion study of BH3120, as a single agent and in combination with pembrolizumab, to assess safety, tolerability, MTD, RP2D, PK, and efficacy in patients with advanced or metastatic solid tumors. Dose-Escalation part is planned to establish the MTD or RD for Dose-Expansion part, while Dose-Expansion part is designed to assess potential efficacy of BH3120, as a single agent and in combination with pembrolizumab, when administered at the RD to subjects in indication-specific expansion cohorts.

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

Talk to the study team

Young Su (Bobby) Noh  ·  82-2-410-9277  ·  63forever@hanmi.co.kr

Always discuss trial participation with your own doctor first.

Locations (10)

Moffitt Cancer CenterTampa, Florida, United StatesRecruiting
The START Center for Cancer Care - MidwestGrand Rapids, Michigan, United StatesRecruiting
Carl & Edyth Lindner Center for Research & Education at The Christ Hospital and The Christ Hospital Cancer CenterCincinnati, Ohio, United StatesRecruiting
Mary Crowley Cancer ResearchDallas, Texas, United StatesWithdrawn
Mays Cancer Center at University of Texas Health San Antonio MD Anderson Cencer CenterSan Antonio, Texas, United StatesRecruiting
Seoul National University Bundang HospitalSeongnam-si, Gyeonggi-do, South KoreaRecruiting
Seoul National University HospitalSeoul, South KoreaRecruiting
Severance HospitalSeoul, South KoreaRecruiting
Asan Medical CenterSeoul, South KoreaRecruiting
Samsung Medical CenterSeoul, South KoreaRecruiting

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Source record: clinicaltrials.gov/study/NCT06234397