Deferasirox

Phase 3Completed

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Interest: 40/100

Hype Score

Development Stage

✓

Pre-clinical

✓

Phase 1

✓

Phase 2

Phase 3

Approved

Indication / Disease

Chronic Iron Overload

Conditions

Chronic Iron Overload

Trial Timeline

Aug 16, 2016 → Jul 23, 2019

NCT ID

NCT02720536

About Deferasirox

Deferasirox is a phase 3 stage product being developed by Novartis for Chronic Iron Overload. The current trial status is completed. This product is registered under clinical trial identifier NCT02720536. Target conditions include Chronic Iron Overload.

What happened to similar drugs?

20 of 20 similar drugs in Chronic Iron Overload were approved

Approved (20) Terminated (3) Active (0)

✅Pegasys® + Pegasys®Chugai PharmaceuticalApproved

✅Telmisartan/Rosuvastatin 40/10mg + Telmisartan 40mgYuhanApproved

✅placebo + aspirin + clopidogrel + aspirin OR prasugrel + aspirinDaiichi SankyoApproved

✅alefacept + polyvalent pneumococcal vaccineAstellas PharmaApproved

✅alefaceptAstellas PharmaApproved

✅AlefaceptAstellas PharmaApproved

✅lysozyme 90 mg + PlaceboEisaiApproved

Hype Score Breakdown

Clinical

Activity

Company

Novelty

Community

Clinical Trials (20)

NCT ID	Phase	Status	Start	Completion	Indication
NCT03387475	Phase 2	Completed	Feb 20, 2018	Oct 1, 2024	Myelodysplasia
NCT03372083	Approved	Completed	Jan 16, 2018	Dec 5, 2019	Iron Overload
NCT02943668	Phase 2	Terminated	Mar 2, 2017	Dec 17, 2018	Anemia
NCT02720536	Phase 3	Completed	Aug 16, 2016	Jul 23, 2019	Chronic Iron Overload
NCT02663752	Phase 2	Terminated	May 30, 2016	Jul 1, 2016	Myelodysplastic Syndrome
NCT02069886	Approved	Withdrawn	Dec 1, 2014	Dec 1, 2018	Thalassemia (Transfusion Delendent)
NCT01948817	Phase 2	Withdrawn	Feb 1, 2014	Feb 1, 2016	Focus on Transfusion Dependent Thalassemia Patients Who Are Inadequate Responders to Deferasirox > 35mg/kgQD
NCT01724138	Approved	Withdrawn	Jun 1, 2013	Oct 1, 2014	β-thalassemia Major
NCT01709838	Approved	Completed	Dec 6, 2012	Jan 17, 2019	Non-transfusion Dependent Thalassemia
NCT01326845	Approved	Terminated	Dec 1, 2011	Sep 1, 2012	Myelodysplastic Syndrome
NCT01394029	Pre-clinical	Completed	Jul 1, 2011	Oct 1, 2015	Transfusional Hemosiderosis
NCT01250951	Approved	Completed	Dec 1, 2009	Sep 1, 2011	Myelodysplastic Syndrome
NCT00981370	Phase 3	Terminated	Apr 1, 2009	Dec 1, 2010	Anemia, Sickle Cell
NCT00879242	Phase 2	Completed	Feb 1, 2009	—	Beta Thalassemia Transfusion Dependent
NCT01335035	Approved	Completed	Dec 1, 2008	—	Iron Overload
NCT00654589	Approved	Completed	Feb 1, 2008	Jan 1, 2012	Iron Overload
NCT00599326	Phase 3	Completed	Jan 1, 2008	Apr 1, 2010	Porphyria Cutanea Tarda
NCT00564941	Approved	Completed	Dec 1, 2007	Jul 1, 2011	Myelodysplastic Syndromes
NCT00673608	Approved	Completed	Nov 1, 2007	Sep 1, 2011	Hemoglobinopathies
NCT00560820	Phase 1	Completed	Sep 1, 2007	Apr 1, 2012	β-thalassemia

Competing Products

20 competing products in Chronic Iron Overload

See all competitors

Product	Company	Stage	Hype Score
Levofloxacin 500	Dr. Reddy's Laboratories	Pre-clinical	23
mRNA-0184	Moderna	Phase 1	0
Lubiprostone + Lubiprostone + Placebo	Dr. Reddy's Laboratories	Phase 3	37
macitentan 10 mg	BML, Inc.	Phase 3	32
KPL-716 + Placebo	Kiniksa Pharmaceuticals	Phase 2	29
TERN-701	Terns Pharmaceuticals	Phase 1/2	36
Fludarabine + Cyclophosphamide + PRGN-3007	Precigen	Phase 1	23
LY3556050 + Placebo	Eli Lilly	Phase 2	35
THB001	Third Harmonic Bio	Phase 1	11
Briquilimab	Jasper Therapeutics	Phase 1/2	26
Briquilimab	Jasper Therapeutics	Phase 1/2	14
Briquilimab	Jasper Therapeutics	Phase 2	29
Empagliflozin + Matching placebo	Eli Lilly	Phase 3	40
LY3461767 + Placebo	Eli Lilly	Phase 1	29
Pirtobrutinib + Venetoclax + Rituximab	Eli Lilly	Phase 3	44
LY3526318 + Placebo	Eli Lilly	Phase 2	35
Pirtobrutinib	Eli Lilly	Phase 2	42
Ibrutinib + LY3214996	Eli Lilly	Phase 1	21
Pirtobrutinib + Acalabrutinib	Eli Lilly	Phase 2	27
LYR-210	Lyra Therapeutics	Phase 2	25