BiotechTube

Pasireotide + Octreotide

Phase 3Completed
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77
Hype Score

Development Stage

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

Acromegaly

Conditions

Acromegaly

Trial Timeline

Feb 11, 2008 → Mar 11, 2016

NCT ID
NCT00600886

About Pasireotide + Octreotide

Pasireotide + Octreotide is a phase 3 stage product being developed by Novartis for Acromegaly. The current trial status is completed. This product is registered under clinical trial identifier NCT00600886. Target conditions include Acromegaly.

Hype Score Breakdown

Clinical
27
Activity
18
Company
10
Novelty
9
Community
10

Clinical Trials (2)

NCT IDPhaseStatus
NCT00690430Phase 3Completed
NCT00600886Phase 3Completed

Competing Products

20 competing products in Acromegaly

See all competitors
ProductCompanyStageHype Score
AlesseNovartisPhase 2
52
ONO-5788 + ONO-5788 Placebo + OctreotideOno PharmaceuticalPhase 1
33
ONO-5788 + [14C]-ONO-5788Ono PharmaceuticalPhase 1
33
Pasireotide LARNovartisPhase 3
77
Octreotide acetate 30 mg suspensionNovartisPhase 3
77
Pasireotide long acting release formulationNovartisPre-clinical
23
Sandostatin LAR + pegvisomant + cabergolineNovartisApproved
85
Octreotide acetate and cabergoline/Octrotide and SomavertNovartisApproved
85
Sandostatin LARNovartisApproved
85
Sandostatin (Octreotide Acetate)NovartisApproved
85
Octreotide acetateNovartisApproved
85
octreotide FluidCrystal® injection depotNovartisPhase 2
52
Octreotide LARNovartisPhase 3
77
Octreotide LARNovartisPhase 3
77
PasireotideNovartisPhase 2
52
Pasireotide LAR 60 mg + PegvisomantNovartisApproved
85
OctreotideNovartisApproved
85
Octreotide LAR 30 MG InjectionNovartisApproved
85
Pasireotide LARNovartisPhase 2
52
Pasireotide (SOM230), Octreotide (Sandostatin)NovartisPhase 2
52

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