tafamidis

Pre-clinicalCompleted
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22
Hype Score

Development Stage

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

Hereditary Transthyretin Amyloidosis (ATTRv) Cardiomyopathy (CM), Mixed Phenotype

Conditions

Hereditary Transthyretin Amyloidosis (ATTRv) Cardiomyopathy (CM), Mixed Phenotype

Trial Timeline

Mar 8, 2023 โ†’ May 19, 2023

About tafamidis

tafamidis is a pre-clinical stage product being developed by Pfizer for Hereditary Transthyretin Amyloidosis (ATTRv) Cardiomyopathy (CM), Mixed Phenotype. The current trial status is completed. This product is registered under clinical trial identifier NCT05139680. Target conditions include Hereditary Transthyretin Amyloidosis (ATTRv) Cardiomyopathy (CM), Mixed Phenotype.

Hype Score Breakdown

Clinical
5
Activity
2
Company
9
Novelty
2
Community
1

Clinical Trials (14)

NCT IDPhaseStatus
NCT06393465Pre-clinicalActive
NCT06086353Pre-clinicalCompleted
NCT05139680Pre-clinicalCompleted
NCT05560555Pre-clinicalCompleted
NCT04814186ApprovedCompleted
NCT03662191Phase 1Completed
NCT03280173Phase 1Completed
NCT03266705Phase 1Completed
NCT02791230Phase 3Completed
NCT02746926Phase 1Completed
NCT02697864Phase 1Completed
NCT01435655Phase 3Completed
NCT00935012Phase 3Completed
NCT00925002Phase 3Completed

Competing Products

20 competing products in Hereditary Transthyretin Amyloidosis (ATTRv) Cardiomyopathy (CM), Mixed Phenotype

See all competitors
ProductCompanyStageHype Score
KVD900KalVista PharmaceuticalsPhase 2
47
KVD824 + Placebo to KVD824KalVista PharmaceuticalsPhase 1
28
KVD900 600 mg + KVD900 300 mgKalVista PharmaceuticalsPhase 3
72
SebetralstatKalVista PharmaceuticalsPre-clinical
18
KVD900 + Placebo to KVD900KalVista PharmaceuticalsPhase 1
28
SebetralstatKalVista PharmaceuticalsPre-clinical
18
Placebo + KVD900 600 mg + KVD900 300 mgKalVista PharmaceuticalsPhase 3
72
KVD824 Prototype 1 modified-release tablet + KVD824 Prototype 2 modified-release tablet + KVD824 Immediate-Release Capsule + Placebo to KVD824 Prototype 1 + KVD824 Prototype 3 modified-release tabletKalVista PharmaceuticalsPhase 1
28
KVD900 150 mg + KVD900 300 mg + KVD900 600 mgKalVista PharmaceuticalsPhase 3
72
KVD824 + Placebo to KVD824KalVista PharmaceuticalsPhase 2
47
KVD900 600 mg + Drug: KVD900 300 mgKalVista PharmaceuticalsPhase 3
72
Deferasirox FCTNovartisPhase 2
52
Canakinumab + PlaceboNovartisPhase 3
77
IlarisNovartisPre-clinical
23
Standard of Care for Haemophilia ARochePre-clinical
23
EmicizumabRochePhase 3
77
TafamidisPfizerPre-clinical
22
NitisinoneSwedish Orphan BiovitrumPre-clinical
22
NitisinoneSwedish Orphan BiovitrumPhase 1
32
NitisinoneSwedish Orphan BiovitrumPre-clinical
22