BH3120
DrugBH3120 will be administered as an IV infusion over 90 minutes on Day 1 of every 3-week treatment cycle
NCT Number: NCT06234397
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 1
Seoul National University Bundang Hospital, Seongnam-si, Gyeonggi-do, South Korea
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
BH3120 will be administered as an IV infusion over 90 minutes on Day 1 of every 3-week treatment cycle
Fixed dose of pembrolizumab will be administered as an IV infusion over 30 minutes on Day 1 of every 3-week treatment cycle
Other names: KEYTRUDA®
Time frame: Throughout the study until end of safety follow-up period (90 days after the last treatment)
To evaluate safety and tolerability of BH3120 as a single agent and in combination with pembrolizumab administration
Time frame: At the end of Cycle 1 (each cycle is 21 days) in Dose-Escalation Part
To evaluate safety and tolerability of BH3120 as a single agent and in combination with pembrolizumab administration
Time frame: Throughout the study until treatment discontinuation (up to 2-3 years)
To evaluate PK profile upon BH3120 administration
Time frame: Throughout the study until treatment discontinuation (up to 2-3 years)
To evaluate PK profile upon BH3120 administration
Time frame: Throughout the study until treatment discontinuation (up to 2-3 years)
To evaluate PK profile upon BH3120 administration
Time frame: Throughout the study until treatment discontinuation (up to 2-3 years)
To evaluate PK profile upon BH3120 administration
Time frame: Throughout the study until treatment discontinuation (up to 2-3 years)
To evaluate PK profile upon BH3120 administration
Time frame: Throughout the study until treatment discontinuation (up to 2-3 years)
To evaluate PK profile upon BH3120 administration
Time frame: Throughout the study until treatment discontinuation (up to 2-3 years)
To evaluate PK profile upon BH3120 administration
Time frame: Throughout the study until treatment discontinuation (up to 2-3 years)
To evaluate PK profile upon BH3120 administration
Time frame: Throughout the study until treatment discontinuation (up to 2-3 years)
Immunogenicity of BH3120
Time frame: Throughout the study until disease progression or death whichever occurs first (up to 2-3 years)
ORR will be measured as the proportion of subjects with a confirmed response of complete response (CR) or partial response (PR) as per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1
Time frame: Throughout the study until disease progression or death whichever occurs first (up to 2-3 years)
DCR will be measured as the proportion of subject with confirmed CR, PR, or Stable Disease (SD) as per RECIST v1.1
Time frame: Throughout the study until disease progression or death whichever occurs first (up to 2-3 years)
DOR will be measured as the time from initial onset of CR or PR to first radiographic progression as per RECIST v. 1.1 or death from any cause, whichever occurs first.
Time frame: Throughout the study until disease progression or death whichever occurs first (up to 2-3 years)
PFS will be measured from date of first treatment until date of radiographic progression as per RECIST v.1.1 or until death from any cause, whichever occurs first
Contact information is provided by the study sponsor or research team.
Hanmi Pharmaceutical Company Limited
Industry
A Phase I, Open-Label, Multinational, Multicenter, Dose Escalation and Expansion Study of BH3120, as a Single Agent and in Combination With Pembrolizumab, in Patients With Advanced or Metastatic Solid Tumors
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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