Golodirsen 50 MG/1 ML Intravenous Solution [VYONDYS 53]

ApprovedTerminated
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80
Hype Score

Development Stage

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

Duchenne Muscular Dystrophy

Conditions

Duchenne Muscular Dystrophy

Trial Timeline

Oct 31, 2020 โ†’ May 13, 2021

About Golodirsen 50 MG/1 ML Intravenous Solution [VYONDYS 53]

Golodirsen 50 MG/1 ML Intravenous Solution [VYONDYS 53] is a approved stage product being developed by Sarepta Therapeutics for Duchenne Muscular Dystrophy. The current trial status is terminated. This product is registered under clinical trial identifier NCT04708314. Target conditions include Duchenne Muscular Dystrophy.

Hype Score Breakdown

Clinical
30
Activity
20
Company
5
Novelty
10
Community
12

Clinical Trials (1)

NCT IDPhaseStatus
NCT04708314ApprovedTerminated

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