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A Trial to Assess Efficacy, Safety, Pharmacokinetics of Octreotide Subcutaneous Injection in Patients With Gastroentero-pancreatic Neuroendocrine Tumor (GEP-NET)

Investigating the Efficacy and Safety of an Investigational Medication in Patients with GEP-NET

Recruiting
18 years and older
All
Phase 2

This study evaluates an investigational medication in patients with gastroentero-pancreatic neuroendocrine tumor (GEP-NET). The purpose of this study is to evaluate the investigational medication compared to Octreotide Microspheres in patients with advanced GEP-NET.

The study will focus on assessing the safety and effectiveness of the investigational medication. It will also look at how the medication is processed in the body, known as pharmacokinetics.

  • Who can participate: Adults aged 18 and older with advanced gastroentero-pancreatic neuroendocrine tumor may be eligible. Participants should have at least one measurable lesion and a history of limited prior treatments.
  • Study details: Participants will receive either the investigational medication or Octreotide Microspheres. The study will compare their effects.
Study details
    Gastrointestinal Neuroendocrine Pancreatic Tumor

NCT06505395

CSPC ZhongQi Pharmaceutical Technology Co., Ltd.

8 April 2026

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