Pasireotide

Phase 1Completed
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Interest: 29/100
29
Hype Score

Development Stage

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

Carcinoid Tumor

Conditions

Carcinoid Tumor, Acromegaly

Trial Timeline

Jun 1, 2006 → Nov 1, 2013

About Pasireotide

Pasireotide is a phase 1 stage product being developed by Novartis for Carcinoid Tumor. The current trial status is completed. This product is registered under clinical trial identifier NCT00446082. Target conditions include Carcinoid Tumor, Acromegaly.

What happened to similar drugs?

1 of 9 similar drugs in Carcinoid Tumor were approved

Approved (1) Terminated (1) Active (7)

Hype Score Breakdown

Clinical
6
Activity
8
Company
15
Novelty
0
Community
0

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 Carcinoid Tumor

See all competitors
ProductCompanyStageHype Score
Ramucirumab + Somatostatin AnalogEli LillyPhase 2
35
Pasireotide + OctreotideNovartisPhase 3
40
Pasireotide (SOM230)NovartisPhase 2
35
Octreotide + Placebo + EverolimusNovartisPhase 3
40
LutatheraNovartisPhase 2
27
EPO906 epothilone BNovartisPhase 2
35
PanitumumabAmgenPhase 2
27
AxitinibPfizerPhase 2
35
Lanreotide + Placebo (for sunitinib) + SunitinibPfizerPhase 2
31
Nivolumab + CabozantinibBristol Myers SquibbPhase 2
35
bevacizumab + 5-fluorouracil + leucovorin + oxaliplatinSanofiPhase 2/3
30
lanreotide Autogel (somatostatin analogue) + Sandostatin long acting release (LAR) Depot (somatostatin analogue)IpsenPhase 3
29
lanreotide (Autogel formulation)IpsenApproved
40
Lanreotide + PlaceboIpsenPhase 3
37
BIM 23A760IpsenPhase 2
24
Randomized: 40 mg Paltusotine + Randomized: 80 mg PaltusotineCrinetics PharmaceuticalsPhase 2
32
Paltusotine + PlaceboCrinetics PharmaceuticalsPhase 3
44
Telotristat etiprate + Placebo-matching telotristat etiprateLexicon PharmaceuticalsPhase 3
34
Telotristat etiprateLexicon PharmaceuticalsPhase 3
34
500 mg [14C]-LX1606Lexicon PharmaceuticalsPhase 1
23