Safety and Efficacy of LCI699 in Cushing's Disease Patients

PHASE2CompletedINTERVENTIONAL
Enrollment

31

Participants

Timeline

Start Date

March 23, 2011

Primary Completion Date

October 22, 2019

Study Completion Date

October 22, 2019

Conditions
Cushings DiseaseCushing Disease
Interventions
DRUG

LCI699

Osilodrostat 1 mg and 5 mg capsules, was prepared by Novartis and supplied to the Investigator. The capsule formulation of osilodrostat was later changed to tablets and this change was implemented in the study with Protocol amendment 6. Osilodrostat was open labeled 1 mg, 5 mg, 10 mg and 20 mg tablets.

Trial Locations (10)

44195

Cleveland Clinic Foundation, Cleveland

75014

Novartis Investigative Site, Paris

80131

Novartis Investigative Site, Napoli

94275

Novartis Investigative Site, Le Kremlin-Bicêtre

60611-3308

Northwestern University Endo, Metabolism and Molecular, Chicago

02114

Massachusetts General Hospital Neuroendocrine Unit, Boston

97239-3098

Oregon Health and Science University SC, Portland

L60020

Novartis Investigative Site, Ancona

060 8648

Novartis Investigative Site, Sapporo

260 8677

Novartis Investigative Site, Chiba

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY