Phuturdex › Diseases › Duchenne muscular dystrophy
Drugs in development · updated 30 October 2026
Duchenne muscular dystrophy: drugs in development
As of 30 October 2026 there are 49 active clinical trials (recruiting or ongoing, phases I–III) on 35 drugs for Duchenne muscular dystrophy. 27 are experimental, that is not yet approved in the United States.
Summary updated every week · data as of 30 October 2026. In Phuturdex you get the full detail of every drug and an email when an alert is published on the ones you follow.
Sign in free →Experimental drugs
Not yet approved by the US FDA for any indication.
| Drug | Most advanced phase | Active trials | Reference trial |
|---|---|---|---|
| AOC 1044 | III | 2 | NCT07587242 |
| Deramiocel | III | 2 | NCT05126758 |
| SGT-003 | III | 2 | NCT07160634 |
| PF-06939926 | III | 1 | NCT04281485 |
| RGX-202 | II–III | 1 | NCT05693142 |
| Zeleciment Rostudirsen | III | 1 | NCT07608432 |
| Sevasemten | II | 3 | NCT06066580 |
| BMN 351 | I–II | 2 | NCT06280209 |
| ENTR-601-44 | I–II | 2 | NCT07037862 |
| ENTR-601-45 | I–II | 2 | NCT07038824 |
| NS-089NCNP-02 | II | 2 | NCT05996003 |
| SAT-3247 | II | 2 | NCT06867107 |
| WVE-N531 | I–II | 2 | NCT04906460 |
| DS-5141b | II | 1 | NCT04433234 |
| DYNE-251 | I–II | 1 | NCT05524883 |
| GNR-097 | I–II | 1 | NCT07673809 |
| KER-065 | II | 1 | NCT07704099 |
| NCNP-03 | I–II | 1 | NCT06053814 |
| NS-050 | I–II | 1 | NCT06053814 |
| SGT-001 | I–II | 1 | NCT03368742 |
| INS1201 | I | 1 | NCT06817382 |
| JWK007 | I | 1 | NCT06114056 |
| BBM-D101 | Early I | 1 | NCT06641895 |
| HG302 | Early I | 1 | NCT06594094 |
| LE051 | Early I | 1 | NCT06900049 |
| RAG-18 | Early I | 1 | NCT07282652 |
| SPOT-03 | Early I | 1 | NCT07188012 |
Sorted by most advanced phase and number of active trials.
Approved drugs in new trials
Approved by the US FDA for at least one indication, not necessarily this disease, and now in active trials on it.
| Drug | Most advanced phase | Active trials | Reference trial |
|---|---|---|---|
| Delandistrogene moxeparvovecElevidys® | III | 4 | NCT05881408 |
| GivinostatDuvyzat® | II–III | 3 | NCT03373968 |
| EteplirsenExondys 51®, Exondys® | III | 1 | NCT03992430 |
| ViltolarsenViltepso® | III | 1 | NCT04768062 |
| SatralizumabEnspryng® | II | 1 | NCT06450639 |
| SemaglutideWegovy, Rybelsus | I–II | 1 | NCT07642635 |
| TadalafilChewtadzy®, Tadliq® | II | 1 | NCT06290713 |
| TacrolimusEnvarsus XR, Prograf® | I | 1 | NCT06692426 |
Sorted by most advanced phase and number of active trials.
All 35 drugs, with the details
In Phuturdex every drug has all its trials, sponsors and countries, FDA and EMA approvals, orphan designations and safety alerts. Free until 31 March 2027.
Open in Phuturdex →Broader categories
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities 4 drugs
- Musculoskeletal disorder 22 drugs
- Nervous System Diseases 39 drugs
- Muscular disease 12 drugs
- X-linked disease 8 drugs
- Atrophic muscular disease 3 drugs
Source: Phuturdex analysis of ClinicalTrials.gov data (U.S. National Library of Medicine), updated 30 October 2026. Active trials = recruiting or ongoing, phases I–III, with at least one identified drug; phase and sites refer to the trials on this disease. Disease name: Wikidata; NLM MeSH term: D020388 “Muscular Dystrophy, Duchenne”. Prevalence: Orphanet.