LAnreotide in Metastatic Pheochromocytoma / PARAganglioma (LAMPARA)

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

June 17, 2019

Primary Completion Date

March 31, 2026

Study Completion Date

March 31, 2026

Conditions
ParagangliomaPheochromocytoma
Interventions
DRUG

Lanreotide

Participants will receive lanreotide 120 mg deep subcutaneous injection every 4 weeks (±7 days) for 52 weeks, followed by an extension phase in which all patients will continue to receive lanreotide 120 mg injection every 4 weeks (±7 days) if there is no evidence of disease progression.

Trial Locations (2)

10032

Columbia University Irving Medical Center, New York

44195

Cleveland Clinic, Cleveland

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Ipsen

INDUSTRY

lead

Antonio Fojo

OTHER

NCT03946527 - LAnreotide in Metastatic Pheochromocytoma / PARAganglioma (LAMPARA) | Biotech Hunter | Biotech Hunter