Study identifier:D081FC00004
ClinicalTrials.gov identifier:NCT04889404
EudraCT identifier:N/A
CTIS identifier:N/A
LYNPARZA Tablets 100 mg, 150mg General drug use-results study in patients on maintenance treatment after platinum-based chemotherapy for BRCA mutated curatively unresectable pancreas cancer
Pancreatic neoplasms
N/A
No
-
All
130
Observational
n/a - n/a
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Apr 2025 by AstraZeneca
AstraZeneca
-
To collect and characterise the incidence of adverse events related to the safety specifications of the maintenance treatment after platinum-based chemotherapy in patients with BRCA mutated pancreatic cancer under the actual post-marketing use of LYNPAZA.
To collect and characterise the incidence of adverse events related to the safety specifications*1 of the maintenance treatment after platinum-based chemotherapy in patients with BRCA mutated pancreatic cancer under the actual post-marketing use of LYNPAZA. This investigation will be conducted for application for re-examination specified in Article 14-4 of the Pharmaceutical Affairs Law. *1: Bone marrow depression, interstitial lung disease, new primary malignancies, and embryofoetal toxicity
Location
Location
Osaka, LYN010001, Japan, D081FC00004
Location
Kanagawa, LYN010003, Japan, D081FC00004
Location
Okayama, LYN010004, Japan, D081FC00004
Location
Niigata, LYN010006, Japan, D081FC00004
Location
Shizuoka, LYN010007, Japan, D081FC00004
Location
Niigata, LYN010008, Japan, D081FC00004
Location
Tokyo, LYN010009, Japan, D081FC00004
Location
Saitama, LYN010010, Japan, D081FC00004
Arms | Assigned Interventions |
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