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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)

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-511271-15-00
Acronym
WO39608
Enrollment
29
Registered
2024-04-04
Start date
2017-11-23
Completion date
2025-02-07
Last updated
2024-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic ductal adenocarcinoma (PDAC)

Brief summary

1. Objective response

Detailed description

1. Progression free survival, 2. Overall survival, 3. Overall survival at specific timepoints, 4. Duration of response, 5. Disease control, 6. Incidence, nature, and severity of adverse events and laboratory abnormalities, 7. Change from baseline in vital signs and ECG parameters, 8. Change from baseline in targeted clinical laboratory test results

Interventions

DRUGAbraxane 5 mg/ml powder for dispersion for infusion.
DRUGRoActemra 20 mg/mL concentrate for solution for infusion
DRUGGemcitabin Kabi 38 mg/ml Pulver zur Herstellung einer Infusionslösung
DRUGAvastin 25 mg/ml concentrate for solution for infusion.
DRUGATEZOLIZUMAB
DRUGTiragolumab

Sponsors

F. Hoffmann-La Roche AG
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
1. Objective response

Secondary

MeasureTime frame
1. Progression free survival, 2. Overall survival, 3. Overall survival at specific timepoints, 4. Duration of response, 5. Disease control, 6. Incidence, nature, and severity of adverse events and laboratory abnormalities, 7. Change from baseline in vital signs and ECG parameters, 8. Change from baseline in targeted clinical laboratory test results

Countries

Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026