LUTATHERA Injection General Use Result Survey

Novartis

Status: Completed

Conditions: Somatostatin Receptor-positive Neuroendocrine Tumor

Treatments: Other: LUTATHERA

Study type: Observational

Funder types: Industry

Identifiers

NCT05844332

CAAA601A11401

Details and patient eligibility

About

This study was a multicenter observational study with a central registration system and all-case surveillance system without a control group.

Full 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 were examined until 40 weeks after the last dose of this drug during the observation period and recorded in the case report forms (CRF).

Enrollment: 347 patients

Sex: All

Ages: 18 to 99 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• All patients treated with this drug for the following indications during a certain post-marketing period

  • Indication: Somatostatin receptor-positive neuroendocrine tumor Patients who started to receive this drug before the contract for this study will also be included in the study population and it will be allowed to register them after the contract so that all patients who receive this drug will be included in this study. Patients treated with this drug for off-label indication will also be included in this study to register all patients received this drug.

Exclusion criteria

• Not applicable

Trial design

347 participants in 1 patient group

LUTATHERA

Description:

patients treated with LUTATHERA Injection

Treatment:

Other: LUTATHERA