Skip to content
Study details
Enrolling now

A Study of ART0380 for Advanced Cancer

Artios Pharma Ltd
NCT IDNCT04657068ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

502

Study length

about 6.1 years

Ages

18+

Locations

40 sites in AL, AR, AZ +18

About this study

This trial is testing a drug called ART0380 in people with advanced or metastatic solid tumors. The goal is to find the best dose of ART0380, learn about its side effects, and see how effective it is when used alone or with gemcitabine or irinotecan.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take ART0380
  • 2.Take Gemcitabine
  • 3.Take Irinotecan
PhasePhase 1/Phase 2
DrugGemcitabine
Routeinjection
Primary goalPart A: Maximum tolerated dose (MTD) by the number of participants with dose limiting toxicities (DLTs) from ART0380 monotherapy and in combination with gemcitabine or irinotecan

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low11%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

gemcitabine, irinotecan

Drug routes

injection (Injection)

Endpoints

Primary: Part A: Maximum tolerated dose (MTD) by the number of participants with dose limiting toxicities (DLTs) from ART0380 monotherapy and in combination with gemcitabine or irinotecan, Part B2: Progression free survival by RECIST 1.1 in participants receiving ART0380 in combination with gemcitabine or gemcitabine alone, Parts B1/B3/B4: Number of participants with adverse events following administration of ART0380 monotherapy and/or in combination with irinotecan at RP2Ds., Parts B5/B6: Object Response Rate (ORR) based on RECIST 1.1 to access anti-tumor activity of ART0380 in combination with irinotecan in each cohort.

Secondary: Part B2: Number of participants with adverse events following administration of ART0380 in combination with gemcitabine or gemcitabine alone, Part B5/B6: Number of participants with adverse events following administration of ART0380 at the RP2D in combination with irinotecan., Parts A1, A2, A3, B1, B3, B4, B5, and B6: Duration of response based on RECIST 1.1, Parts A1, A2, A3, B1, B3, B4, B5, and B6: Progression free survival based on RECIST 1.1, Parts A1, A2, A3, B1, B3, B4: Objective response rate based on RECIST 1.1, Parts B1/B3/B4/B5/B6: Overall Survival, Pharmacokinetic Analysis (multiple dose): Area Under The Curve Plasma Concentration Time Curve from zero to 12 hours (AUC0-12 ss) in a steady state., Pharmacokinetic Analysis (multiple dose): Area Under The Curve Plasma Concentration Time Curve from zero to the time of last plasma concentration (AUC0-t ss) in a steady state.

Body systems

Oncology