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A Trial to Assess Efficacy and Safety of Octreotide Subcutaneous Depot in Patients With GEP-NET

Study acronym: SORENTO
StatusActive, Not Recruiting
PhasePhase 3
SponsorCamurus AB
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 3 months later Jul 2026 → Nov 2026
See other at-risk trials from Camurus AB

Record History

  1. Minor Primary completion pushed from Jul 2026 to Nov 2026
    • Study completion pushed from Jul 2028 to Nov 2028
    v20
  2. Minor Study sites: 98 to 86v19
  3. Notable Primary completion date: Dec 2025 to Jul 2026
    • Study completion date: Dec 2027 to Jul 2028
    v18
  4. Notable Primary completion date: Dec 2024 to Dec 2025
    • Study completion date: Dec 2026 to Dec 2027
    v17
  5. Minor Trial status: Recruiting to Active, Not Recruiting
    • Enrollment target: estimated 300 to confirmed 332
    • Study sites: 103 to 98
    v16
Show 14 earlier versionsHide 14 earlier versions
  1. Minor Study sites: 101 to 103v15
  2. Minor Study sites: 99 to 101v14
  3. Minor Study sites: 95 to 99v13
  4. Minor Study sites: 89 to 95v12
  5. Minor Study sites: 83 to 89v11
  6. Minor Study sites: 73 to 83v10
  7. Minor Study sites: 56 to 73v9
  8. Minor Study sites: 42 to 56v8
  9. Minor Study sites: 33 to 42v7
  10. Minor Study sites: 14 to 33v6
  11. Minor Study sites: 9 to 14v5
  12. Minor Study sites: 8 to 9v4
  13. Minor Study sites: 6 to 8v3
  14. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 6
    • Start date changed from estimate of Sep 2021 to Oct 22, 2021
    v2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
4 trials monitored
See 1 trial at risk
The purpose of this study is to compare the effectiveness and safety of CAM2029 to octreotide LAR or lanreotide ATG in patients with advanced, well-differentiated GEP-NET. Patients who experience progressive disease in the randomized part of the study may proceed to an open-label extension part with intensified treatment with CAM2029.
Trial Details
NCT Number NCT05050942
Lead Sponsor Camurus AB
Conditions
(from sponsor)
Gastro-enteropancreatic Neuroendocrine Tumor
Related terms Gastro-enteropancreatic neuroendocrine tumor
Enrollment 332 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov