DDrare: Database of Drug Development for Rare Diseases

Searched query = "Muscular dystrophy", "Dystrophinopathies", "Myotilinopathy", "Laminopathy", "Caveolinopathy", "LGMD1C", "Desminopathy", "Sarcoglycanopathy", "α-dystroglycanopathy", "FCMD", "Walker-Warburg syndrome", "Muscle-eye-brain disease", "Myotonic dystrophy", "Integrin α7 deficient CMD", "Rigid spine syndrome"
The queries were searched in Public_title, Scientific_title, and Condition. Export date: 03/15/2021. Trials are sorted by Date_enrollment from most recent to oldest in the table.

Drug = (+)- Epicatechin; (+)-Epicatechin; (-)-Epicatechin; (-)-epicatechin; 12 mg/kg GSK2402968; 2011-2012 seasonal flu vaccine Intramuscular; 2011-2012 seasonal flu vaccine Subcutaneous; 29180.00.00, 34681.00.00, 34681.01.00, 34681.02.00; 3 mg/kg GSK2402968; 4-Benzyl-2-naphthalen-1-yl-1,2,4- thiadiazolidine-3,5-dione; 4-benzyl-2-naphthalen-1-yl-1,2,4-thiadiazolidine-3,5-dione; 5-(ethylsulfonyl)-2-(naphthalen-2-yl)benzo[d]oxazole; 6 mg/kg GSK2402968; 750 mg metformin and 7.5 g L-citrulline daily p.o.; 9 mg/kg GSK2402968; AAV1-gamma-sarcoglycan vector injection; 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); ACE-031 0.5 mg/kg q4wk; ACE-031 1.0 mg/kg q2wk; ACE-083; ASP0367; ATALUREN; ATYR1940; AVI-4658; AVI-4658 (Eteplirsen); AVI-4658 (PMO); AVI-4658 for Injection; Acetate; Actonel Once a week 5mg film coated tablets; Adeno-associated viral vector serotype 9 containing the human mini-dystrophin gene; Albuterol; Allogeneic Cardiosphere-Derived Cells (CAP-1002); Anti-Myostatin Adnectin; Anti-myostati; Anti-myostatin Adnectin; Arginine; Aspirin; Ataluren; Ataluren 1000 mg; Ataluren 125 mg; Ataluren 250 mg; Autologous bone marrow mononuclear cell transplantation; BIO101; BLS-M22; BMN 044; BMN 044 IV 6 mg/kg; BMN 044 IV 9 mg/kg; BMN 044 SC 6 mg/kg; BMN 045; BMN 053; BMN053; BMS-986089; BMS-986089-01 (RO7239361) , anti-myostatin; BMS-986089-01 (RO7239361) Injections, 15 mg/Syringe (21.4 mg/mL); BMS-986089-01 (RO7239361) Injections, 35 mg/Syringe (50 mg/mL); BMS-986089-01 (RO7239361) Injections, 50 mg/Syringe (71.4 mg/mL); BMS-986089-01 (RO7239361) Injections, 7.5 mg/Syringe (10.7 mg/mL); BMS-986089-01 (RO7239361), anti-myostatin; BMS-986089-01 Injections, 15 mg/Syringe (21.4 mg/mL); BMS-986089-01 Injections, 35 mg/Syringe (50 mg/mL); BMS-986089-01 Injections, 50 mg/Syringe (71.4 mg/mL); BMS-986089-01 Injections, 7.5 mg/Syringe (10.7 mg/mL); BMS-986089-01, Anti-myostatin; BMS-986089-01, anti-myostatin; BOTULINUM TOXIN TYPE A; Balance; Behavioral: In-home Exercise Training; Behavioral: Regular exercise; Biological: Umbilical Cord Based Allogenic Mesenchymal Stem Cell; Bisoprolol; Bisoprolol Fumarate; Bisphosphonate treatment; Blood test; Botulinum toxin type A; CALCIFEDIOL; CAP-1002; CARVEDILOL; CASIMERSEN; CAT-1004; CRD007; Cabaletta; Calcichew D3 Forte; Calcifediol; Canakinumab; Canakinumab Injection [Ilaris]; Cardicor; Cardicor (Merck brand); Cardiovascular profile; Carvedilol; Casimersen; Chronic Corticosteroid Therapy; Cialis 10 mg film-coated tablets; Cialis 2.5 mg film-coated tablets; Cialis 20 mg film-coated tablets; Cialis 5 mg film-coated tablets; Citrulline; Coenzyme Q10; Coenzyme Q10 and Lisinopril; Cosyntropin; Cosyntropin acetate; Cr13C; Creatine; Creatine Monohydrate; Creatine monohydrate; Creatine-13C; Cyclosporin; Cyclosporin A; DEFLAN*10CPR 6MG; DEFLAZACORT; DELTACORTENE*20CPR 5MG; DHA; DILATREND; DRISAPERSEN SODIUM; DS-5141b; Decortin; Deflazacort; Deflazacort 6 mg Tablets; Dehydroepiandrosterone; Dehydroepiandrosterone 100 and 400 mg; Device: Activity Monitor; Dexmedetomidine; Diagnostic Test: 30 seconds sit to stand test; Diagnostic Test: Beck depression inventory; Diagnostic Test: Berg balance scale; Diagnostic Test: Brief Pain Inventory Short-Form; Diagnostic Test: DM1-ActivC; Diagnostic Test: Fatigue and Daytime Sleepiness Scale; Diagnostic Test: Functional Index-2; Diagnostic Test: GSGC; Diagnostic Test: Hand opening time; Diagnostic Test: Manual muscle testing; Diagnostic Test: McGill pain questionnaire; Diagnostic Test: Myotonia (from Individualised Neuromuscular Quality of Life Questionnaire); Diagnostic Test: Myotonia Behaviour scale; Diagnostic Test: Pressure pain threshold; Diagnostic Test: Quantitative muscle testing; Diagnostic Test: Quick motor function test; Diagnostic Test: R-PAct; Diagnostic Test: Scale for Assessment and Rating of Ataxia; Diagnostic Test: Six minute walking test; Dosing Extension; Drisapersen; EDASALONEXENT; EDG-5506; EGCG; EMD 87580; EMEA/H/C/000638; EMFLAZA® (DEFLAZACORT); EMFLAZA® (deflazacort); ENALAPRIL; EPA; EPA and DHA; ERX-963; ETEPLIRSEN; EV substance code: SUB188638; EXONDYS 51™; Edasalonexent; EnaHexal; EnaHexal®, 10mg; EnalHexal®, 5 mg; Enalapril; Epicatechin; Epigallocatechin; Epigallocatechin-Gallate; Eplerenone; Eteplirsen; Eteplirsen Injection; Eucardic; Exondys 51; Ezutromid; FG-3019; FTX-1821; Filgrastim; Flavocoxid; GIVINOSTAT; GIVINOSTAT (hyrochloride monohydrate); GOLODIRSEN; GSK2402968; GSK2402968 3mg/kg/week; GSK2402968 6 mg/kg/week; GSK2402968 6mg/kg/week; Genetic: RNA extraction; Gentamicin; Gentamicin infusions twice a week for six months; Givinostat; Givinostat (hydrochloride monohydrate); Givinostat (idrocloruro monoidrato); Glutamine; Gold; Golodirsen; Granulocyte colony-stimulating factor (Filgrastim); Guanidine; H44AON188; H51AON23; HIDROFEROL; HLA-identical allogeneic mesoangioblasts; HMABs; HT-100; Haemostasis tests; Hidroferol; Hidroferol®; Hormonal profile; Human Umbilical Cord Mesenchymal Stem Cells; Human umbilical cord mesenchymal stem cells; IBUPROFEN; IBUPROFEN 200MG; IDEBENONE; IGF-1; IONIS-DMPKRx; ISOSORBIDE DINITRATE; ITF2357; Ibuprofen; Idebenone; Idebenone 150 mg film-coated tablets; Ifetroban; Inflammatory profile; Isosorbide; Isosorbide Dinitrate; Isosorbide Dinitrate 20 mg; Isosorbide Dinitrate 40 mg; Isosorbide Dinitrate 60 mg; Isosorbide Dinitrate 80 mg; Isosorbide dinitrate; Ketamine; L-Arginine; L-Citrulline and Metformin & L-Citrulline; L-Glutamine; L-arginine; LOSMAPIMOD; Lentiviral Vector Trans-Skip gene modified Autologous Mesoangioblasts; Lisinopril; Lonafarnib; Losartan; Losmapimod; METFORMIN; METFORMINA - 500 30 COMPRESSE 500 MG; METOPROLOL SUCCINATE; MNK-1411; MONITOR; MYO-029; MYODM; Metabolic profile; Metformin; Metformin 500mg; Metformin and Metformin & L-Citrulline; Metformina; Methylphenidate; MetoHEXAL® Succ ® 23,75 mg Retardtabletten; MetoHEXAL® Succ ® 47,5 mg Retardtabletten; MetoHEXAL® Succ ® 95 mg Retardtabletten; Metoprolol; Mexiletine; Monocytes and megacaryocytes culture and RNA extraction; Myoblast autologous graft; Myoblast transplantation; Myoblastes autologues; N(4,5Bis methanesulfonyl2methylbenzoyl) guanidine hydrochloride monohydrate; N-(4,5-Bis methanesulfonyl-2-methyl-benzoyl)guanidine hydrochloride monohydrate; NPC-14; NS-065/NCNP-01; NS-089/NCNP-02; Nanosuspension); Nebivolol; Needle biopsy of the vastus lateralis muscle; Nitrate; Nébivolol; Oligomero morfolino fosforodiamidato per skipping dell’esone 45; Oligomero morfolino fosforodiamidato per skipping dell’esone 53; Omigapil; Other: Dystrophin levels; Other: Echocardiogram; Other: Ibuprofen and Isosorbide Dinitrate combination; Other: Magnetic Resonance Imaging (MRI); Other: Metabolic Exercise Testing using stationary bicycle; Other: Pulmonary Function Testing (PFT); Other: Standard steroid treatment; Other: beetroot juice extract; Oxatomide; Oxatomide (tinset); P-188 NF; PAMREVLUMAB; PB1046 Injection; PEMIROLAST; PF-06252616; PF-06939926; PFT; PRD2175434; PREDNISONE; PRO044; PRO044 IV; PRO044 IV 6 mg/kg; PRO044 IV 9 mg/kg; PRO044 SC; PRO044 SC 6 mg/kg; PRO045; PRO045, 0.15 mg/kg/week; PRO045, 1.0 mg/kg/week; PRO045, 3.0 mg/kg/week; PRO045, 6.0 mg/kg/week; PRO045, 9.0 mg/kg/week; PRO045, selected dose; PRO051; PRO053; PS188; PS188 (company code); PS220; PS524; PTC0161480, PTC124 Compound 1a, RPS2505, PTC-C124, 291844; PTC124; Pamrevlumab; Pamrevlumab (FG-3019); Pemirolast; Pending; Pentoxifylline; Peptide-conjugated phosphorodiamidate morpholino oligomer for exon 51 skipping; Perindopril; Perindopril 2mg Tablets; Phosphorodiamidate Morpholino Oligomer; Phosphorodiamidate morpholino oligomer for exon 45 skipping; Phosphorodiamidate morpholino oligomer for exon 53 skipping; Powder for Oral Suspension); Prednisolone; Prednison; Prednisone; Prednisone 5 mg tablets; Procedure: Increased exercise intensity; Procedure: Saline injection; Procedure: Taking of blood; Protein-carbohydrate supplementation; RAAV1.CMV.huFollistatin344; RAAV1.CMV.huFollistin344; RAAV2.5-CMV-minidystrophin (d3990); RAAV9-CK8-h-µD5; RAAVrh74.MCK.GALGT2; RAAVrh74.MCK.micro-Dystrophin; RAXONE - 150 MG- COMPRESSE RIVESTITE CON FILM- USO ORALE- FLACONE (HDPE)- 180 COMPRESSE; RO7239361; RO7239361 (BMS-986089); RO7239361 Injections, 15 mg/Syringe (21.4 mg/mL); RO7239361 Injections, 35 mg/Syringe (50 mg/mL); RO7239361 Injections, 50 mg/Syringe (71.4 mg/mL); RO7239361 Injections, 7.5 mg/Syringe (10.7 mg/mL); Ramipril; Ranolazine; Raxone; Recombinant human anti-GDF-8 antibody; Regimen Selection Phase Group 1 (COMPLETED); Regimen Selection Phase Group 2; Regimen Selection Phase Group 3; Resveratrol; Revatio; RhIGF-I/rhIGFBP-3; RhIGFBP-3; Rimeporide; Risedronate; Risedronate sodium; SGT-001; SMT C1100; SMT C1100 (F5; SMT C1100 (F5); SMT C1100 (F6; SMT C1100 (F6); SNT-MC17; SRP-4045; SRP-4053; SRP-5051; Sandimmun Optoral; ScAAV9.U7.ACCA; ScAAVrh74.tMCK.hSGCA; Sildenafil; Sleep parameters; Sodium Nitrate; Sodium Nitrate - double dose; Sodium nitrate; SomatoKine/IPLEX; Somatropin; Spironolactone; Stem Cell; Stem Cells; Sunphenon; Sunphenon EGCG; Sustanon; Sustanon (testosterone); Sustanon 250; Suvodirsen; TADALAFIL; TAMOX; TAMOXIFEN; TAMOXIFEN CITRATE; TAS-205; TETRACOSACTIDE HEXAACETATE; TRIATEC; Tacrolimus; Tadalafil; Tadalafil 20 MG; Tadalafil and Sildenafil; Tamoxifen; Tamoxifen 20mg Hexal® Filmtabletten; Tehalose 30gr; Temerit; Testosterone; Testosterone Enanthate; Testosterone decanoate; Testosterone enanthate; Testosterone isocaproate; Testosterone phenylpropionate; Testosterone propionate; Tetracosactide; Tideglusib; Tinset; Tranilast; Translarna; Translarna 1000 mg granules for oral suspension; Translarna 125 mg granules for oral suspension; Translarna 250 mg granules for oral suspension; Treatment Phase Group 4; Trehalose; Triatec; Umbilical Cord Mesenchymal Stem Cell; Umbilical Cord Mesenchymal Stem Cells; VAMOROLONE; VBP15; VILTOLARSEN; Vamarolone; Vamorolone; Vamorolone 0.25 mg/day/day; Vamorolone 0.25 mg/kg/day; Vamorolone 0.75 mg/day/day; Vamorolone 0.75 mg/kg/day; Vamorolone 2.0 mg/day/day; Vamorolone 2.0 mg/kg/day; Vamorolone 6.0 mg/day/day; Vamorolone 6.0 mg/kg/day; Viltolarsen; Vit C Vit E Zn Se; WVE-210201; WVE-210201 (suvodirsen); Xeomin; Zn; [WVE-210201]

No.	TrialID	Date_ enrollment	Date_ registration	Public_title	Scientific_title	Condition	Intervention	Primary_ sponsor	Secondary_ sponsor	Recruitment_ Status	Inclusion_ agemin	Inclusion_ agemax	Inclusion_ gender	Target_ size	Phase	Countries
1	EUCTR2019-003563-22-IE (EUCTR)	23/06/2020	21/01/2020	A study to provide Edasalonexent to Pediatric Patients with Duchenne Muscular Dystrophy	An Open-Label Extension Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy	Duchenne Muscular Dystrophy MedDRA version: 20.0;Level: PT;Classification code 10013801;Term: Duchenne muscular dystrophy;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]	Product Name: Edasalonexent Product Code: CAT-1004 INN or Proposed INN: EDASALONEXENT	Catabasis Pharmaceuticals Inc.	NULL	Not Recruiting			Female: no Male: yes	140	Phase 3	United States;Canada;Ireland;Australia;Germany;United Kingdom;Sweden
2	EUCTR2019-003563-22-GB (EUCTR)	23/04/2020	13/01/2020	A study to provide Edasalonexent to Pediatric Patients with Duchenne Muscular Dystrophy	An Open-Label Extension Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy - An Open-Label Extension Study of Edasalonexent in DMD Patients	Duchenne Muscular Dystrophy MedDRA version: 20.0;Level: PT;Classification code 10013801;Term: Duchenne muscular dystrophy;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]	Product Name: Edasalonexent Product Code: CAT-1004 INN or Proposed INN: EDASALONEXENT	Catabasis Pharmaceuticals Inc.	NULL	Not Recruiting			Female: no Male: yes	140	Phase 3	United States;Canada;Ireland;Australia;Germany;United Kingdom;Sweden
3	EUCTR2019-003563-22-DE (EUCTR)	16/04/2020	31/01/2020	A study to provide Edasalonexent to Pediatric Patients with Duchenne Muscular Dystrophy	An Open-Label Extension Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy	Duchenne Muscular Dystrophy MedDRA version: 20.0;Level: PT;Classification code 10013801;Term: Duchenne muscular dystrophy;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]	Product Name: Edasalonexent Product Code: CAT-1004 INN or Proposed INN: EDASALONEXENT	Catabasis Pharmaceuticals Inc.	NULL	Authorised-recruitment may be ongoing or finished			Female: no Male: yes	140	Phase 3	United States;Canada;Ireland;Australia;Israel;Germany;United Kingdom;Sweden
4	EUCTR2019-003563-22-SE (EUCTR)	15/04/2020	03/02/2020	A study to provide Edasalonexent to Pediatric Patients with Duchenne Muscular Dystrophy	An Open-Label Extension Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy	Duchenne Muscular Dystrophy MedDRA version: 20.0;Level: PT;Classification code 10013801;Term: Duchenne muscular dystrophy;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]	Product Name: Edasalonexent Product Code: CAT-1004 INN or Proposed INN: EDASALONEXENT	Catabasis Pharmaceuticals Inc.	NULL	Not Recruiting			Female: no Male: yes	140	Phase 3	United States;Canada;Ireland;Australia;Germany;United Kingdom;Sweden
5	NCT03917719 (ClinicalTrials.gov)	March 14, 2019	12/4/2019	An Open-Label Extension Study of Edasalonexent in Boys With Duchenne Muscular Dystrophy	An Open-Label Extension Study of Edasalonexent in Pediatric Patients With Duchenne Muscular Dystrophy	Duchenne Muscular Dystrophy	Drug: Edasalonexent	Catabasis Pharmaceuticals	NULL	Terminated	4 Years	12 Years	Male	130	Phase 3	United States;Australia;Canada;Germany;Sweden;United Kingdom
No.	TrialID	Date_ enrollment	Date_ registration	Public_title	Scientific_title	Condition	Intervention	Primary_ sponsor	Secondary_ sponsor	Recruitment_ Status	Inclusion_ agemin	Inclusion_ agemax	Inclusion_ gender	Target_ size	Phase	Countries
6	EUCTR2018-000464-29-DE (EUCTR)	31/01/2019	24/09/2018	A study to compare edasalonexent with placebo in patients with Duchenne Muscular dystrophy	A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, GLOBAL PHASE 3 STUDY OF EDASALONEXENT IN PEDIATRIC PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY - POLARIS DMD	Duchenne muscular dystrophy MedDRA version: 20.0;Level: PT;Classification code 10013801;Term: Duchenne muscular dystrophy;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]	Product Name: Edasalonexent Product Code: CAT-1004 INN or Proposed INN: EDASALONEXENT Product Name: Edasalonexent Product Code: CAT-1004 INN or Proposed INN: EDASALONEXENT	Catabasis Pharmaceuticals, Inc.	NULL	Authorised-recruitment may be ongoing or finished			Female: no Male: yes	126	Phase 3	United States;Canada;Ireland;Australia;Israel;Germany;United Kingdom;Sweden
7	EUCTR2018-000464-29-IE (EUCTR)	16/01/2019	02/10/2018	A study to compare edasalonexent with placebo in pediatric patients with Duchenne Muscular dystrophy.	A RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, GLOBAL PHASE 3 STUDY OFEDASALONEXENT IN PEDIATRIC PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY - Phase 3 Study of Edasalonexent in Duchenne Muscular Dystrophy	Duchenne Muscular Dystrophy MedDRA version: 20.0;Level: PT;Classification code 10013801;Term: Duchenne muscular dystrophy;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]	Product Name: Edasalonexent Product Code: CAT-1004 INN or Proposed INN: Edasalonexent	Catabasis Pharmaceuticals, Inc.	NULL	Not Recruiting			Female: no Male: yes	126	Phase 3	United States;Canada;Ireland;Australia;Israel;Germany;United Kingdom;Sweden
8	EUCTR2018-000464-29-SE (EUCTR)	11/12/2018	24/09/2018	A study to compare edasalonexent with placebo in patients with Duchenne Muscular dystrophy.	A RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, GLOBAL PHASE 3 STUDY OFEDASALONEXENT IN PEDIATRIC PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY - POLARIS DMD	Duchenne Muscular Dystrophy MedDRA version: 20.0;Level: PT;Classification code 10013801;Term: Duchenne muscular dystrophy;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]	Product Name: Edasalonexent Product Code: CAT-1004 INN or Proposed INN: Edasalonexent	Catabasis Pharmaceuticals, Inc.	NULL	Not Recruiting			Female: no Male: yes	126	Phase 3	Canada;Ireland;Australia;Israel;Germany;United Kingdom;Sweden;United States
9	NCT03703882 (ClinicalTrials.gov)	October 2, 2018	8/10/2018	Phase III Study of Edasalonexent in Boys With Duchenne Muscular Dystrophy	A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients With Duchenne Muscular Dystrophy	Muscular Dystrophy, Duchenne	Drug: Edasalonexent;Drug: Placebo	Catabasis Pharmaceuticals	NULL	Completed	4 Years	7 Years	Male	131	Phase 3	United States;Australia;Canada;Germany;Ireland;Israel;Sweden;United Kingdom
10	NCT02439216 (ClinicalTrials.gov)	April 2016	29/4/2015	Phase 1/2 Study in Boys With Duchenne Muscular Dystrophy	A Phase 1/2 Study of Edasalonexent (CAT-1004) in Pediatric Patients With Duchenne Muscular Dystrophy	Muscular Dystrophy, Duchenne	Drug: Edasalonexent;Drug: Placebo	Catabasis Pharmaceuticals	NULL	Completed	4 Years	7 Years	Male	31	Phase 1;Phase 2	United States

No.

TrialID

Date_
enrollment

Date_
registration

Public_title

Scientific_title

Condition

Intervention

Primary_
sponsor

Secondary_
sponsor

Recruitment_
Status

Inclusion_
agemin

Inclusion_
agemax

Inclusion_
gender

Target_
size

Phase

Countries

EUCTR2019-003563-22-IE
(EUCTR)

23/06/2020

21/01/2020

A study to provide Edasalonexent to Pediatric Patients with Duchenne Muscular Dystrophy

An Open-Label Extension Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy

Duchenne Muscular Dystrophy
MedDRA version: 20.0;Level: PT;Classification code 10013801;Term: Duchenne muscular dystrophy;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]

Product Name: Edasalonexent
Product Code: CAT-1004
INN or Proposed INN: EDASALONEXENT

Catabasis Pharmaceuticals Inc.

NULL

Not Recruiting

Female: no
Male: yes

140

Phase 3

United States;Canada;Ireland;Australia;Germany;United Kingdom;Sweden

EUCTR2019-003563-22-GB
(EUCTR)

23/04/2020

13/01/2020

A study to provide Edasalonexent to Pediatric Patients with Duchenne Muscular Dystrophy

An Open-Label Extension Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy - An Open-Label Extension Study of Edasalonexent in DMD Patients

Product Name: Edasalonexent
Product Code: CAT-1004
INN or Proposed INN: EDASALONEXENT

Catabasis Pharmaceuticals Inc.

NULL

Not Recruiting

Female: no
Male: yes

140

Phase 3

United States;Canada;Ireland;Australia;Germany;United Kingdom;Sweden

EUCTR2019-003563-22-DE
(EUCTR)

16/04/2020

31/01/2020

A study to provide Edasalonexent to Pediatric Patients with Duchenne Muscular Dystrophy

An Open-Label Extension Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy

Product Name: Edasalonexent
Product Code: CAT-1004
INN or Proposed INN: EDASALONEXENT

Catabasis Pharmaceuticals Inc.

NULL

Authorised-recruitment may be ongoing or finished

Female: no
Male: yes

140

Phase 3

United States;Canada;Ireland;Australia;Israel;Germany;United Kingdom;Sweden

EUCTR2019-003563-22-SE
(EUCTR)

15/04/2020

03/02/2020

A study to provide Edasalonexent to Pediatric Patients with Duchenne Muscular Dystrophy

An Open-Label Extension Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy

Product Name: Edasalonexent
Product Code: CAT-1004
INN or Proposed INN: EDASALONEXENT

Catabasis Pharmaceuticals Inc.

NULL

Not Recruiting

Female: no
Male: yes

140

Phase 3

United States;Canada;Ireland;Australia;Germany;United Kingdom;Sweden

NCT03917719
(ClinicalTrials.gov)

March 14, 2019

12/4/2019

An Open-Label Extension Study of Edasalonexent in Boys With Duchenne Muscular Dystrophy

An Open-Label Extension Study of Edasalonexent in Pediatric Patients With Duchenne Muscular Dystrophy

Duchenne Muscular Dystrophy

Drug: Edasalonexent

Catabasis Pharmaceuticals

NULL

Terminated

4 Years

12 Years

Male

130

Phase 3

United States;Australia;Canada;Germany;Sweden;United Kingdom

No.

TrialID

Date_
enrollment

Date_
registration

Public_title

Scientific_title

Condition

Intervention

Primary_
sponsor

Secondary_
sponsor

Recruitment_
Status

Inclusion_
agemin

Inclusion_
agemax

Inclusion_
gender

Target_
size

Phase

Countries

EUCTR2018-000464-29-DE
(EUCTR)

31/01/2019

24/09/2018

A study to compare edasalonexent with placebo in patients with Duchenne Muscular dystrophy

A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, GLOBAL PHASE 3 STUDY OF EDASALONEXENT IN PEDIATRIC PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY - POLARIS DMD

Duchenne muscular dystrophy
MedDRA version: 20.0;Level: PT;Classification code 10013801;Term: Duchenne muscular dystrophy;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]

Product Name: Edasalonexent
Product Code: CAT-1004
INN or Proposed INN: EDASALONEXENT
Product Name: Edasalonexent
Product Code: CAT-1004
INN or Proposed INN: EDASALONEXENT

Catabasis Pharmaceuticals, Inc.

NULL

Authorised-recruitment may be ongoing or finished

Female: no
Male: yes

126

Phase 3

United States;Canada;Ireland;Australia;Israel;Germany;United Kingdom;Sweden

EUCTR2018-000464-29-IE
(EUCTR)

16/01/2019

02/10/2018

A study to compare edasalonexent with placebo in pediatric patients with Duchenne Muscular dystrophy.

A RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, GLOBAL PHASE 3 STUDY OFEDASALONEXENT IN PEDIATRIC PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY - Phase 3 Study of Edasalonexent in Duchenne Muscular Dystrophy

Product Name: Edasalonexent
Product Code: CAT-1004
INN or Proposed INN: Edasalonexent

Catabasis Pharmaceuticals, Inc.

NULL

Not Recruiting

Female: no
Male: yes

126

Phase 3

United States;Canada;Ireland;Australia;Israel;Germany;United Kingdom;Sweden

EUCTR2018-000464-29-SE
(EUCTR)

11/12/2018

24/09/2018

A study to compare edasalonexent with placebo in patients with Duchenne Muscular dystrophy.

A RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, GLOBAL PHASE 3 STUDY OFEDASALONEXENT IN PEDIATRIC PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY - POLARIS DMD

Product Name: Edasalonexent
Product Code: CAT-1004
INN or Proposed INN: Edasalonexent

Catabasis Pharmaceuticals, Inc.

NULL

Not Recruiting

Female: no
Male: yes

126

Phase 3

Canada;Ireland;Australia;Israel;Germany;United Kingdom;Sweden;United States

NCT03703882
(ClinicalTrials.gov)

October 2, 2018

8/10/2018

Phase III Study of Edasalonexent in Boys With Duchenne Muscular Dystrophy

A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients With Duchenne Muscular Dystrophy

Muscular Dystrophy, Duchenne

Drug: Edasalonexent;Drug: Placebo

Catabasis Pharmaceuticals

NULL

Completed

4 Years

7 Years

Male

131

Phase 3

United States;Australia;Canada;Germany;Ireland;Israel;Sweden;United Kingdom

NCT02439216
(ClinicalTrials.gov)

April 2016

29/4/2015

Phase 1/2 Study in Boys With Duchenne Muscular Dystrophy

A Phase 1/2 Study of Edasalonexent (CAT-1004) in Pediatric Patients With Duchenne Muscular Dystrophy

Muscular Dystrophy, Duchenne

Drug: Edasalonexent;Drug: Placebo

Catabasis Pharmaceuticals

NULL

Completed

4 Years

7 Years

Male

Phase 1;Phase 2

United States