347
Participants
Start Date
December 17, 2021
Primary Completion Date
June 27, 2024
Study Completion Date
June 27, 2024
LUTATHERA
There is no treatment allocation. Patients administered LUTATHERA by prescription can be enrolled.
Novartis Investigative Site, Nagoya
Novartis Investigative Site, Hirosaki
Novartis Investigative Site, Kamogawa
Novartis Investigative Site, Kashiwa
Novartis Investigative Site, Tōon
Novartis Investigative Site, Fukuoka
Novartis Investigative Site, Fukushima
Novartis Investigative Site, Gifu
Novartis Investigative Site, Maebashi
Novartis Investigative Site, Sapporo
Novartis Investigative Site, Sapporo
Novartis Investigative Site, Akashi
Novartis Investigative Site, Kobe
Novartis Investigative Site, Kanazawa
Novartis Investigative Site, Kita-gun
Novartis Investigative Site, Kagoshima
Novartis Investigative Site, Kamakura
Novartis Investigative Site, Yokohama
Novartis Investigative Site, Sendai
Novartis Investigative Site, Suwa
Novartis Investigative Site, Kurashiki
Novartis Investigative Site, Okayama
Novartis Investigative Site, Osaka
Novartis Investigative Site, Ōsaka-sayama
Novartis Investigative Site, Suita
Novartis Investigative Site, Hamamatsu
Novartis Investigative Site, Iwata
Novartis Investigative Site, Sunto Gun
Novartis Investigative Site, Bunkyo-ku
Novartis Investigative Site, Chuo Ku
Novartis Investigative Site, Koto Ku
Novartis Investigative Site, Chūō
Novartis Investigative Site, Chiba
Novartis Investigative Site, Fukui
Novartis Investigative Site, Fukuoka
Novartis Investigative Site, Hiroshima
Novartis Investigative Site, Kobe
Novartis Investigative Site, Kumamoto
Novartis Investigative Site, Kyoto
Novartis Investigative Site, Niigata
Novartis Investigative Site, Osaka
Novartis Investigative Site, Osaka
Novartis Investigative Site, Shizuoka
Novartis Investigative Site, Tokushima
Novartis Investigative Site, Toyama
Novartis Investigative Site, Yamagata
Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY