Ataluren

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

Duchenne Muscular Dystrophy

Conditions

Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, Dystrophinopathy

Trial Timeline

May 20, 2012 → Jan 19, 2018

About Ataluren

Ataluren is a phase 3 stage product being developed by PTC Therapeutics for Duchenne Muscular Dystrophy. The current trial status is completed. This product is registered under clinical trial identifier NCT01557400. Target conditions include Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, Dystrophinopathy.

What happened to similar drugs?

2 of 19 similar drugs in Duchenne Muscular Dystrophy were approved

Approved (2) Terminated (8) Active (10)
Tadalafil + PlaceboEli LillyPhase 3
🔄Viltolarsen + PlaceboNippon ShinyakuPhase 3
🔄ViltolarsenNippon ShinyakuPhase 3
🔄Ataluren + PlaceboPTC TherapeuticsPhase 3
🔄Ataluren + PLACEBOPTC TherapeuticsPhase 3
AtalurenPTC TherapeuticsPhase 3

Hype Score Breakdown

Clinical
17
Activity
8
Company
12
Novelty
0
Community
0

Clinical Trials (13)

NCT IDPhaseStatus
NCT04336826Phase 2Completed
NCT03796637Phase 2Completed
NCT04117880Phase 2Withdrawn
NCT03648827Phase 2Completed
NCT02819557Phase 2Completed
NCT02456103Phase 3Terminated
NCT02107859Phase 3Terminated
NCT02090959Phase 3Terminated
NCT01557400Phase 3Completed
NCT01247207Phase 3Completed
NCT01140451Phase 3Completed
NCT00458341Phase 2Completed
NCT00237380Phase 2Completed

Competing Products

20 competing products in Duchenne Muscular Dystrophy

See all competitors
ProductCompanyStageHype Score
Phase 1, SQY51 + Phase 2a, SQY51 (cohort 1) + Phase 2a, SQY51 (cohort 2) + Phase 2a, SQY51 (cohort 3)BiotrialPhase 1/2
29
ENTR-601-44 + ENTR-601-44 - matching placeboEntrada TherapeuticsPhase 1/2
29
ENTR-601-45 + ENTR-601-45 - matching placeboEntrada TherapeuticsPhase 1/2
29
Tadalafil + PlaceboEli LillyPhase 3
32
DS-5141bDaiichi SankyoPhase 2
39
DS-5141bDaiichi SankyoPhase 1/2
32
Bocidelpar + PlaceboAstellas PharmaPhase 1
21
scAAV9.U7.ACCAAstellas PharmaPhase 1/2
32
NS-065/NCNP-01Nippon ShinyakuPhase 2
35
Viltolarsen + PlaceboNippon ShinyakuPhase 3
40
ViltolarsenNippon ShinyakuPhase 2
35
NS-089/NCNP-02 + NS-089/NCNP-02Nippon ShinyakuPhase 2
39
NS-065/NCNP-01Nippon ShinyakuPhase 1
29
NS-050/NCNP-03 + PlaceboNippon ShinyakuPhase 1/2
39
NS-089/NCNP-02Nippon ShinyakuPhase 2
42
ViltolarsenNippon ShinyakuPhase 3
36
NS-089/NCNP-02Nippon ShinyakuPhase 1/2
32
NS-065/NCNP-01 + PlaceboNippon ShinyakuPhase 2
35
ACE-031 0.5 mg/kg q4wk + ACE-031 1.0 mg/kg q2wkMerckPhase 2
27
ACE-031 (Extension of cohort 1 from core study, A031-03) + ACE-031 (Extension of cohort 2 from core study, A031-03) + ACE-031 (Extension of cohort 3 from core study, A031-03)MerckPhase 2
27