Pasireotide LAR

Phase 3Completed
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77
Hype Score

Development Stage

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

Acromegaly

Conditions

Acromegaly

Trial Timeline

Mar 31, 2015 โ†’ Sep 27, 2018

About Pasireotide LAR

Pasireotide LAR 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 NCT02354508. Target conditions include Acromegaly.

Hype Score Breakdown

Clinical
27
Activity
18
Company
10
Novelty
9
Community
10

Clinical Trials (5)

NCT IDPhaseStatus
NCT02354508Phase 3Completed
NCT01283542Phase 2Completed
NCT01673646Phase 2Completed
NCT01364415Phase 1Completed
NCT00958841Phase 2Terminated

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AlesseNovartisPhase 2
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ONO-5788 + ONO-5788 Placebo + OctreotideOno PharmaceuticalPhase 1
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ONO-5788 + [14C]-ONO-5788Ono PharmaceuticalPhase 1
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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
Pasireotide + OctreotideNovartisPhase 3
77
Sandostatin (Octreotide Acetate)NovartisApproved
85
Octreotide acetateNovartisApproved
85
octreotide FluidCrystalยฎ 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