Pasireotide

Phase 2Completed
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52
Hype Score

Development Stage

Pre-clinical
Phase 1
3
Phase 2
4
Phase 3
5
Approved
Indication / Disease

Cushing Disease

Conditions

Cushing Disease

Trial Timeline

Aug 13, 2004 → Jul 8, 2013

About Pasireotide

Pasireotide is a phase 2 stage product being developed by Novartis for Cushing Disease. The current trial status is completed. This product is registered under clinical trial identifier NCT00171951. Target conditions include Cushing Disease.

Hype Score Breakdown

Clinical
17
Activity
12
Company
10
Novelty
5
Community
5

Clinical Trials (8)

NCT IDPhaseStatus
NCT03103009Phase 1Completed
NCT02780882Phase 2Withdrawn
NCT01617733Phase 2Terminated
NCT00698464Phase 1Completed
NCT00434148Phase 3Completed
NCT00446082Phase 1Completed
NCT00171730Phase 2Completed
NCT00171951Phase 2Completed

Competing Products

20 competing products in Cushing Disease

See all competitors
ProductCompanyStageHype Score
AZD4017 and prednisolone + Placebo Oral Tablet and prednisoloneAstraZenecaPhase 2
52
Pasireotide with or without cabergolineNovartisPhase 2
52
osilodrostat + LCI699 matching placeboNovartisPhase 3
77
pasireotide LAR + SOM230 LAR 30 mg + SOM230 LAR 10 mgNovartisPhase 3
77
LCI699NovartisPhase 2
52
Pasireotide sub-cutaneousNovartisPhase 3
77
osilodrostat + osilodrostat PlaceboNovartisPhase 3
77
OsilodrostatNovartisPhase 2
52
PasireotideNovartisPhase 3
77
Pasireotide s.c. + Sitagliptin + Liraglutide + Insulin + Pasireotide LAR + MetforminNovartisApproved
85
SOM230 s.c.NovartisPhase 2
52
Lu AG13909LundbeckPhase 2
49
OsilodrostatRecordatiPre-clinical
20
Intervention/TreatmentRecordatiApproved
82
PasireotideRecordatiPre-clinical
20
LCI699RecordatiPhase 2
49
Pasireotide + Cabergoline + Pasireotide LARRecordatiApproved
82
OsilodrostatRecordatiPre-clinical
20
osilodrostatRecordatiPhase 2
49
OsilodrostatRecordatiPre-clinical
20