A Real-world Study of Liposomal Irinotecan (Onivyde)-Based Therapy in Patients With Locally Advanced/Metastatic Pancreatic Cancer in China

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorRenJi Hospital

About this trial

This study is designed to evaluate the real world efficacy and safety of the liposomal irinotecan (Onivyde®)-based treatment scheme in Chinese patients with locally advanced or metastatic pancreatic cancer, and to compare the efficacy with that of the whole pancreatic cancer population who did not receive relevant treatment.

Eligibility criteria

Qualifiers

Age ≥ 18 years old.

Patients with locally advanced or metastatic PDAC diagnosed by pathology.

Patients who received at least one cycle of Nal-IRI (Onivyde®)+ 5-FU/LV treatment.

Patients who have progressed in treatment with gemcitabine or gemcitabine containing regimens in the past.

Disqualifiers

Confirm pregnant or lactating women.

The patient's clinical data is not available.

The researchers determined that they were not suitable for inclusion in the study due to other circumstances.

Trial design

Treatments tested in this trial

  • Nal-IRI (Onivyde®)-based treatment
  • Other second-line treatment

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators

RenJi Hospital

Lead sponsor

Servier (Tianjin) Pharmaceutical Co. LTD.

Collaborator