Product
CAM2029
Aliases
CAM2029 (octreotide subcutaneous depot), octreotide subcutaneous depot
Name
Mycapssa
INN Name
OCTREOTIDE ACETATE
FDA Approved
Yes
4 clinical trials
3 organizations
3 indications
2 documents
Indication
Polycystic Liver DiseaseIndication
AcromegalyClinical trial
A Randomized, Multi-center, Open-label, Active-controlled Phase 3 Trial to Assess the Efficacy and Safety of Octreotide Subcutaneous Depot (CAM2029) Versus Octreotide LAR or Lanreotide ATG in Patients With GEP-NETStatus: Active (not recruiting), Estimated PCD: 2024-12-01
Clinical trial
A Randomized, Placebo-controlled, Double-blind, Multi-center Trial to Assess Efficacy and Safety of Octreotide Subcutaneous Depot (CAM2029) in Patients With Symptomatic Polycystic Liver DiseaseStatus: Active (not recruiting), Estimated PCD: 2025-02-01
Clinical trial
A Phase 3, Open-label, Single-arm, Multi-center Trial to Assess the Long-term Safety of Octreotide Subcutaneous Depot (CAM2029) in Patients With AcromegalyStatus: Active (not recruiting), Estimated PCD: 2025-06-01
Clinical trial
A Phase 3, Randomized, Double-blind, Placebo-controlled, Multi-center Trial to Assess Efficacy and Safety of Octreotide Subcutaneous Depot (CAM2029) in Patients With AcromegalyStatus: Completed, Estimated PCD: 2023-05-02
Document
DailyMed Label: MycapssaOrganization
Chiesi USA, Inc.Document
DailyMed Label: Octreotide
Organization
Fresenius Kabi USA, LLC