CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 341 enrolled
Drug / intervention
Nab-Paclitaxel +14 moredrug
Likely dose
Not stated in record
Key inclusion· 9
  • Histologically or cytologically confirmed metastatic pancreatic ductal adenocarcinoma
  • ECOG performance status 0 or 1
  • Cohort 1: no prior systemic treatment for PDAC
  • Cohort 2: disease progression during administration of 5-FU- or gemcitabine-based first-line chemotherapy
Key exclusion· 10
  • Symptomatic, untreated, or actively progressing CNS metastases
  • History of leptomeningeal disease
  • Active or history of autoimmune disease or immune deficiency
  • History of idiopathic pulmonary fibrosis, organizing pneumonia, drug-induced pneumonitis, or idiopathic pneumonitis, or evidence of active pneumonitis on screening chest CT

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03193190
NCT03193190Phase 2Completed

A Phase Ib/II, Open-Label, Multicenter, Randomized Umbrella Study Evaluating the Efficacy and Safety of Multiple Immunotherapy-Based Treatment Combinations in Patients With Metastatic Pancreatic Ductal Adenocarcinoma (Morpheus-Pancreatic Cancer)

Hoffmann-La Roche·interventional·Posted Jun 20, 2017·Updated Nov 21, 2025

In Brief

A Phase 2 clinical trial evaluating Nab-Paclitaxel, Gemcitabine, and 13 other interventions for Pancreatic Adenocarcinoma. Completed, enrolled 341 participants across 23 sites in 5 countries.

Detailed Summary

A Phase Ib/II, open-label, multicenter, randomized study designed to assess the safety, tolerability, pharmacokinetics and preliminary anti-tumor activity of immunotherapy-based treatment combinations in participants with metastatic Pancreatic Ductal Adenocarcinoma (PDAC). Two cohorts will be enrolled in parallel in this study: Cohort 1 will consist of patients who have received no prior systemic therapy for metastatic PDAC, and Cohort 2 will consist of patients who have received one line of prior systemic therapy for PDAC. In each cohort, eligible patients will be assigned to one of several treatment arms.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesGermany, Japan, South Korea, Spain, United States
Collaborators--

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedJun 20, 2017
Enrollment StartJul 5, 2017
Primary CompletionFeb 27, 2025
TodayJul 2, 2026
Enrollment to primary: 7.6 yearsPosted 9.0 years ago

Interventions

Nab-Paclitaxeldrug

Nab-Paclitaxel will be administered as per the schedule specified in the respective arm.

Gemcitabinedrug

Gemcitabine will be administered as per the schedule specified in the respective arm.

Oxaliplatindrug

Oxaliplatin will be administered as per the schedule specified in the respective arm.

Leucovorindrug

Leucovorin will be administered as per the schedule specified in the respective arm.

Fluorouracildrug

Fluorouracil will be administered as per the schedule specified in the respective arm.

Atezolizumabdrug

Atezolizumab will be administered as per the schedule specified in the respective arm.

Cobimetinibdrug

Cobimetinib will be administered as per the schedule specified in the respective arm.

PEGPH20drug

PEGPH20 will be administered as per the schedule specified in the respective arm.

BL-8040drug

BL-8040 will be administered as per the schedule specified in the respective arm.

Selicrelumabdrug

Selicrelumab will be administered as per the schedule specified in the respective arm.

Bevacizumabdrug

Bevacizumab will be administered as per the schedule specified in the respective arm.

RO6874281drug

RO6874281 will be administered as per the schedule specified in the respective arm

AB928drug

AB928 will be administered as per the schedule specified in the respective arm.

Tiragolumabdrug

Tiragolumab will be administered as per the schedule specified in the respective arm.

Tocilizumabdrug

Tocilizumab will be administered as per the schedule specified in the respective arm.