TrialSignal
Clinical trial intelligence report
Phase II Study to Evaluate the Efficacy and Safety of 177Lu-Dotatate in the First-line Treatment of Inoperable Patients With Locally Advanced or Metastatic, Somatostatin Receptor-positive G2 or G3 Gastroenteropancreatic Neuroendocrine Tumors
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 25, 2026
Report code
NCT05894486-Jun 25, 2026
NCT ID
NCT05894486
Status
UNKNOWN
Phase
Phase 2
Sponsor
Peking University
Executive brief
Investment-Ready Snapshot
The Phase II trial of Lutetium[177Lu] Oxodotreotide Injection, sponsored by Peking University, aims to establish the efficacy and safety of this treatment in patients with unresectable or metastatic GEP-NETs. Given the increasing prevalence of neuroendocrine tumors and the limited treatment options available, successful outcomes could position this therapy as a first-line treatment, potentially capturing significant market share in the oncology sector. The competitive landscape includes existing therapies such as somatostatin analogs and other peptide receptor radionuclide therapies (PRRTs). The trial's results may influence future treatment guidelines and reimbursement decisions, making it a critical asset for stakeholders in the oncology market.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05894486
Indication
Neuroendocrine Tumors
Modality
small molecule
Target
Somatostatin receptor-positive G2 or G3 gastroenteropancreatic neuroendocrine tumors (GEP-NETs)
Intervention
Lutetium[177Lu] Oxodotreotide Injection
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.