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Study details
Enrolling now

JAB-23E73 Trial

Jacobio Pharmaceuticals Co., Ltd.
NCT IDNCT06973564ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

294

Study length

about 2.8 years

Ages

18+

Locations

4 sites in MN, MO, OH +1

What this study is about

Researchers are testing JAB-23E73 in adults with advanced solid tumors that have a KRAS alteration. The trial will evaluate the safety and tolerability of this medication as a single treatment.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take JAB-23E73

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Dose Escalation (Phase 1a): Determine the Maximum tolerated dose (MTD) of JAB-23E73 monotherapy., Dose Escalation (Phase 1a): Evaluate the overall safety and tolerability of JAB-23E73.

Secondary: Dose Escalation (Phase 1a): Overall Response Rate (ORR), Dose Escalation (Phase 1a): Pharmacokinetics (PK): Maximum Observed Concentration (Cmax), Dose Expansion/Optimization (Phase 1b): Evaluate the overall safety and tolerability of JAB-23E73., Dose Expansion/Optimization (Phase 1b): Overall Response Rate (ORR), Dose Expansion/Optimization (Phase 1b): Pharmacokinetics (PK): Maximum Observed Concentration (Cmax)