A Study of IMC-002 in Patients With Advanced Cancer Failed to Standard Therapy

PHASE1RecruitingINTERVENTIONAL
Enrollment

62

Participants

Timeline

Start Date

June 2, 2022

Primary Completion Date

December 17, 2027

Study Completion Date

August 30, 2029

Conditions
Advanced Cancer
Interventions
BIOLOGICAL

IMC-002

Part 1: Dose escalation IMC-002 5, 10, 20, and 30 mg/kg over 3 hours (±30 minutes) intravenous (IV) infusion every 2 weeks Part 2: Expansion cohort IMC-002 20 mg/kg over 3 hours (±30 minutes) IV infusion at the first cycle, if the first infusion is tolerated, then over 1 to 1.5 hours (±10 minutes) IV infusion at all following cycles every 3 weeks In hepatocellular (HCC) Cohort, Lenvatinib 8 mg once daily (body weight of \< 60 kg), or 12 mg once daily (body weight of ≥ 60 kg) In triple negative breast cancer (TNBC) Cohort, Paclitaxel 175 mg/m2 IV infusion on Day 1 of each cycle, or Gemcitabine 1,000 mg/m2 followed by Carboplatin AUC 2 IV infusion on Day 1 and Day 8 of each cycle In biliary tract cancer (BTC) Cohort, Lenvatinib 8 mg once daily (body weight of \< 60 kg), or 12 mg once daily (body weight of ≥ 60 kg) In B-cell lymphoma Cohort, Rituximab 375 mg/m2 IV infusion on Day 1 of each cycle

Trial Locations (3)

Unknown

RECRUITING

National Cancer Center, Ilsan

RECRUITING

Asan Medical Center, Republic of Korea, Seoul

RECRUITING

Samsung Medical Center, Seoul

Sponsors
All Listed Sponsors
lead

ImmuneOncia Therapeutics Inc.

INDUSTRY

NCT05276310 - A Study of IMC-002 in Patients With Advanced Cancer Failed to Standard Therapy | Biotech Hunter | Biotech Hunter