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Tranexamic acid first, than placebo + First placebo, than Tranexamic acid.

Phase 3Completed
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Interest: 37/100
37
Hype Score

Development Stage

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

Hereditary Hemorrhagic Telangiectasia

Conditions

Hereditary Hemorrhagic Telangiectasia

Trial Timeline

Mar 1, 2002 → Oct 1, 2002

NCT ID
NCT01031992

About Tranexamic acid first, than placebo + First placebo, than Tranexamic acid.

Tranexamic acid first, than placebo + First placebo, than Tranexamic acid. is a phase 3 stage product being developed by Baxter for Hereditary Hemorrhagic Telangiectasia. The current trial status is completed. This product is registered under clinical trial identifier NCT01031992. Target conditions include Hereditary Hemorrhagic Telangiectasia.

What happened to similar drugs?

2 of 20 similar drugs in Hereditary Hemorrhagic Telangiectasia were approved

Approved (2) Terminated (0) Active (18)
🔄KVD900 600 mg + KVD900 300 mgKalVista PharmaceuticalsPhase 3
🔄Placebo + KVD900 600 mg + KVD900 300 mgKalVista PharmaceuticalsPhase 3
🔄KVD900 150 mg + KVD900 300 mg + KVD900 600 mgKalVista PharmaceuticalsPhase 3
🔄KVD900 600 mg + Drug: KVD900 300 mgKalVista PharmaceuticalsPhase 3
🔄Canakinumab + PlaceboNovartisPhase 3
🔄EmicizumabRochePhase 3
🔄NitisinoneSwedish Orphan BiovitrumPhase 3

Hype Score Breakdown

Clinical
17
Activity
8
Company
12
Novelty
0
Community
0

Clinical Trials (1)

NCT IDPhaseStatus
NCT01031992Phase 3Completed

Competing Products

20 competing products in Hereditary Hemorrhagic Telangiectasia

See all competitors
ProductCompanyStageHype Score
KVD900KalVista PharmaceuticalsPhase 2
29
KVD824 + Placebo to KVD824KalVista PharmaceuticalsPhase 1
23
KVD900 600 mg + KVD900 300 mgKalVista PharmaceuticalsPhase 3
38
SebetralstatKalVista PharmaceuticalsPre-clinical
20
KVD900 + Placebo to KVD900KalVista PharmaceuticalsPhase 1
23
SebetralstatKalVista PharmaceuticalsPre-clinical
24
Placebo + KVD900 600 mg + KVD900 300 mgKalVista PharmaceuticalsPhase 3
34
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
23
KVD900 150 mg + KVD900 300 mg + KVD900 600 mgKalVista PharmaceuticalsPhase 3
34
KVD824 + Placebo to KVD824KalVista PharmaceuticalsPhase 2
21
KVD900 600 mg + Drug: KVD900 300 mgKalVista PharmaceuticalsPhase 3
38
Deferasirox FCTNovartisPhase 2
27
Canakinumab + PlaceboNovartisPhase 3
40
IlarisNovartisPre-clinical
33
Standard of Care for Haemophilia ARochePre-clinical
26
EmicizumabRochePhase 3
40
TafamidisPfizerPre-clinical
26
tafamidisPfizerPre-clinical
26
NitisinoneSwedish Orphan BiovitrumPre-clinical
26
NitisinoneSwedish Orphan BiovitrumPhase 1
29