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Spots Global Cancer Trial Database for LUTATHERA Injection General Use Result Survey

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Trial Identification

Brief Title: LUTATHERA Injection General Use Result Survey

Official Title: LUTATHERA Injection General Use Result Survey (Somatostatin Receptor-positive Neuroendocrine Tumor, CAAA601A11401)

Study ID: NCT05844332

Interventions

LUTATHERA

Study Description

Brief Summary: This study is a multicenter observational study with a central registration system and all-case surveillance system without a control group.

Detailed Description: From the date of the first dose of this drug until 40 weeks after the date of the last dose (64 weeks if 4 doses are administered 8 weeks apart). For patients who discontinue treatment with this drug during the observation period, necessary variables will be examined until 40 weeks after the last dose of this drug during the observation period and recorded in the case report forms (CRF).

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Novartis Investigative Site, Nagoya, Aichi, Japan

Novartis Investigative Site, Hirosaki, Aomori, Japan

Novartis Investigative Site, Kamogawa, Chiba, Japan

Novartis Investigative Site, Kashiwa, Chiba, Japan

Novartis Investigative Site, Toon city, Ehime, Japan

Novartis Investigative Site, Fukuoka city, Fukuoka, Japan

Novartis Investigative Site, Fukushima city, Fukushima, Japan

Novartis Investigative Site, Gifu-city, Gifu, Japan

Novartis Investigative Site, Maebashi city, Gunma, Japan

Novartis Investigative Site, Sapporo city, Hokkaido, Japan

Novartis Investigative Site, Sapporo, Hokkaido, Japan

Novartis Investigative Site, Akashi, Hyogo, Japan

Novartis Investigative Site, Kobe-city, Hyogo, Japan

Novartis Investigative Site, Kobe-shi, Hyogo, Japan

Novartis Investigative Site, Kanazawa-city, Ishikawa, Japan

Novartis Investigative Site, Kita-gun, Kagawa, Japan

Novartis Investigative Site, Kagoshima city, Kagoshima, Japan

Novartis Investigative Site, Kamakura-city, Kanagawa, Japan

Novartis Investigative Site, Yokohama-city, Kanagawa, Japan

Novartis Investigative Site, Kumamoto City, Kumamoto, Japan

Novartis Investigative Site, Sendai city, Miyagi, Japan

Novartis Investigative Site, Suwa, Nagano, Japan

Novartis Investigative Site, Kurashiki-city, Okayama, Japan

Novartis Investigative Site, Okayama-city, Okayama, Japan

Novartis Investigative Site, Osaka Sayama, Osaka, Japan

Novartis Investigative Site, Osaka-city, Osaka, Japan

Novartis Investigative Site, Suita, Osaka, Japan

Novartis Investigative Site, Hamamatsu-city, Shizuoka, Japan

Novartis Investigative Site, Iwata City, Shizuoka, Japan

Novartis Investigative Site, Shizuoka-city, Shizuoka, Japan

Novartis Investigative Site, Sunto Gun, Shizuoka, Japan

Novartis Investigative Site, Bunkyo-ku, Tokyo, Japan

Novartis Investigative Site, Chuo ku, Tokyo, Japan

Novartis Investigative Site, Koto ku, Tokyo, Japan

Novartis Investigative Site, Toyama-city, Toyama, Japan

Novartis Investigative Site, Chuo-city, Yamanashi, Japan

Novartis Investigative Site, Chiba, , Japan

Novartis Investigative Site, Fukui, , Japan

Novartis Investigative Site, Fukuoka, , Japan

Novartis Investigative Site, Hiroshima, , Japan

Novartis Investigative Site, Kyoto, , Japan

Novartis Investigative Site, Niigata, , Japan

Novartis Investigative Site, Osaka, , Japan

Novartis Investigative Site, Osaka, , Japan

Novartis Investigative Site, Tokushima, , Japan

Novartis Investigative Site, Yamagata, , Japan

Contact Details

Name: Novartis Pharmaceuticals

Affiliation: Novartis Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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