Muscular Dystrophy Drugs in Development by Stages, Target, MoA, RoA, Molecule Type and Key Players, 2022 Update

Muscular Dystrophy Drugs in Development by Stages, Target, MoA, RoA, Molecule Type and Key Players, 2022 Update

Summary

Global Markets Direct's latest Pharmaceutical and Healthcare disease pipeline guide Muscular Dystrophy - Drugs In Development, 2022, provides an overview of the Muscular Dystrophy (Musculoskeletal Disorders) pipeline landscape.

Muscular dystrophy is a group of diseases in which muscle fibers are unusually susceptible to damage. These damaged muscles become progressively weaker. Symptoms usually appear before age 6 and may appear as early as infancy. They may include fatigue, learning difficulties, intellectual disability, muscle weakness and progressive difficulty walking.

Report Highlights

Global Markets Direct's Pharmaceutical and Healthcare latest pipeline guide Muscular Dystrophy - Drugs In Development, 2022, provides comprehensive information on the therapeutics under development for Muscular Dystrophy (Musculoskeletal Disorders), complete with analysis by stage of development, drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. The guide covers the descriptive pharmacological action of the therapeutics, its complete research and development history and latest news and press releases.

The Muscular Dystrophy (Musculoskeletal Disorders) pipeline guide also reviews of key players involved in therapeutic development for Muscular Dystrophy and features dormant and discontinued projects. The guide covers therapeutics under Development by Companies /Universities /Institutes, the molecules developed by Companies in Phase III, Phase II, Phase I, IND/CTA Filed, Preclinical and Discovery stages are 4, 10, 9, 1, 52 and 29 respectively. Similarly, the Universities portfolio in Phase II, Preclinical and Discovery stages comprises 2, 6 and 8 molecules, respectively.

Muscular Dystrophy (Musculoskeletal Disorders) pipeline guide helps in identifying and tracking emerging players in the market and their portfolios, enhances decision making capabilities and helps to create effective counter strategies to gain competitive advantage. The guide is built using data and information sourced from Global Markets Direct’s proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations and featured press releases from company/university sites and industry-specific third party sources. Additionally, various dynamic tracking processes ensure that the most recent developments are captured on a real time basis.

Note: Certain content / sections in the pipeline guide may be removed or altered based on the availability and relevance of data.

Scope

  • The pipeline guide provides a snapshot of the global therapeutic landscape of Muscular Dystrophy (Musculoskeletal Disorders).
  • The pipeline guide reviews pipeline therapeutics for Muscular Dystrophy (Musculoskeletal Disorders) by companies and universities/research institutes based on information derived from company and industry-specific sources.
  • The pipeline guide covers pipeline products based on several stages of development ranging from pre-registration till discovery and undisclosed stages.
  • The pipeline guide features descriptive drug profiles for the pipeline products which comprise, product description, descriptive licensing and collaboration details, R&D brief, MoA & other developmental activities.
  • The pipeline guide reviews key companies involved in Muscular Dystrophy (Musculoskeletal Disorders) therapeutics and enlists all their major and minor projects.
  • The pipeline guide evaluates Muscular Dystrophy (Musculoskeletal Disorders) therapeutics based on mechanism of action (MoA), drug target, route of administration (RoA) and molecule type.
  • The pipeline guide encapsulates all the dormant and discontinued pipeline projects.
  • The pipeline guide reviews latest news related to pipeline therapeutics for Muscular Dystrophy (Musculoskeletal Disorders)
Reasons to Buy
  • Procure strategically important competitor information, analysis, and insights to formulate effective R&D strategies.
  • Recognize emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage.
  • Find and recognize significant and varied types of therapeutics under development for Muscular Dystrophy (Musculoskeletal Disorders).
  • Classify potential new clients or partners in the target demographic.
  • Develop tactical initiatives by understanding the focus areas of leading companies.
  • Plan mergers and acquisitions meritoriously by identifying key players and it’s most promising pipeline therapeutics.
  • Formulate corrective measures for pipeline projects by understanding Muscular Dystrophy (Musculoskeletal Disorders) pipeline depth and focus of Indication therapeutics.
  • Develop and design in-licensing and out-licensing strategies by identifying prospective partners with the most attractive projects to enhance and expand business potential and scope.
  • Adjust the therapeutic portfolio by recognizing discontinued projects and understand from the know-how what drove them from pipeline.


Introduction
Global Markets Direct Report Coverage
Muscular Dystrophy – Overview
Muscular Dystrophy – Therapeutics Development
Pipeline Overview
Pipeline by Companies
Pipeline by Universities/Institutes
Products under Development by Companies
Products under Development by Universities/Institutes
Muscular Dystrophy – Therapeutics Assessment
Assessment by Target
Assessment by Mechanism of Action
Assessment by Route of Administration
Assessment by Molecule Type
Muscular Dystrophy – Companies Involved in Therapeutics Development
Achelios Therapeutics Inc
Altay Therapeutics Inc
Amicus Therapeutics Inc
AMO Pharma Ltd
Anima Biotech Inc
Antisense Therapeutics Ltd
ARMGO Pharma Inc
Arrowhead Pharmaceuticals Inc
ARTHEx Biotech SL
Asklepios BioPharmaceutical Inc
Astellas Gene Therapies
Atamyo Therapeutics SAS
Avidity Biosciences Inc
Beech Tree Labs Inc
Benitec Biopharma Inc
Biophytis SA
Bioprojet SCR
CalyGene Biotechnology Inc
CANbridge Life Sciences Ltd
Casma Therapeutics Inc
Celularity Inc
Chugai Pharmaceutical Co Ltd
Constant Therapeutics LLC
CRISPR Therapeutics AG
Debiopharm International SA
Design Therapeutics Inc
DR.Noah Biotech Inc
Dyne Therapeutics Inc
Edgewise Therapeutics Inc
Elixirgen Therapeutics Inc
Entrada Therapeutics Inc
Enzerna Biosciences LLC
Epicrispr Biotechnologies Inc
EpiSwitch Rx Inc
Exodos Life Sciences Limited Partnership
Expansion Therapeutics Inc
F. Hoffmann-La Roche Ltd
Facio Therapies BV
Faze medicines
Fulcrum Therapeutics Inc
Generian Pharmaceuticals Inc
Healx Ltd
Hope Biosciences LLC
Juvena Therapeutics Inc
Keros Therapeutics Inc
LinkedUp Bioscience Inc
Locanabio Inc
Loqus23 Therapeutics Ltd
Lupin Ltd
ML Bio Solutions Inc
Modalis Therapeutics Corp
Myocea Inc
Myogem Health Company SL
NeuBase Therapeutics Inc
Nexien Biopharma Inc
Nippon Shinyaku Co Ltd
Nymirum Inc
Pasithea Therapeutics Corp
Pepgen Inc
Pfizer Inc
Phrixus Pharmaceuticals Inc
Prothelia Inc
QiXia Decode Therapeutics
Recursion Pharmaceuticals Inc
SanBio Co Ltd
Sanofi
Santhera Pharmaceuticals Holding AG
Sarcomed AB
Sarepta Therapeutics Inc
Scriptr Global Inc
SEAL Therapeutics AG
Seelos Therapeutics, Inc.
Siwa Therapeutics Inc
Syros Pharmaceuticals Inc
Triplet Therapeutics Inc
Vertex Pharmaceuticals Inc
Vita Therapeutics Inc
Xonovo Inc
Muscular Dystrophy – Drug Profiles
alisporivir – Drug Profile
alpha-tocopherol – Drug Profile
Antisense Oligonucleotide to Inhibit DUX4 for Facioscapulohumeral Muscular Dystrophy – Drug Profile
Antisense RNAi Oligonucleotide to Inhibit DUX4 for Facioscapulohumeral Muscular Dystrophy – Drug Profile
AOC-1001 – Drug Profile
AOC-1020 – Drug Profile
ARM-210 – Drug Profile
ARODUX-4 – Drug Profile
ARTHEx-01 – Drug Profile
AT-466 – Drug Profile
ATA-100 – Drug Profile
ATA-200 – Drug Profile
ATL-1102 – Drug Profile
BB-301 – Drug Profile
BIO-103 – Drug Profile
Calpain 3 – Drug Profile
Cell Therapy for Autoimmune Disorders, Cardiovascular Disorders, CNS Disorders, Infectious Disease, Musculoskeletal Disorders and Oncology – Drug Profile
CG-10052 – Drug Profile
CIP-137401 – Drug Profile
CRI-007 – Drug Profile
DM – Drug Profile
DM1 Program – Drug Profile
domagrozumab – Drug Profile
Drugs for Myotonic Dystrophy – Drug Profile
DYNE-101 – Drug Profile
Dyne-102 – Drug Profile
DYNE-301 – Drug Profile
EDG-5506 – Drug Profile
Emery-Dreifuss muscular dystrophy Type 1 – Drug Profile
ENTR-701 – Drug Profile
ENZ-003 – Drug Profile
EPIC-321 – Drug Profile
ERX-963 – Drug Profile
erythromycin – Drug Profile
Facioscapulohumeral Muscular Dystrophy (FSHD) – Drug Profile
FM-10 – Drug Profile
Gene Therapies for Friedreich Ataxia and Myotonic Dystrophy – Drug Profile
Gene Therapy for Genetic Disorders, Neurology, Musculoskeletal and Ophthalmology – Drug Profile
Gene Therapy for Muscular Dystrophy – Drug Profile
Gene Therapy for Myotonic Dystrophy – Drug Profile
Gene Therapy to Activate DMPK for Myotonic Dystrophy Type 1 – Drug Profile
Gene Therapy to Activate Dystrophin for Muscular Dystrophy – Drug Profile
Gene Therapy to Activate ZSCAN4 for Muscular Dystrophy – Drug Profile
Gene Therapy To Inhibit DMPK for Myotonic Dystrophy – Drug Profile
Gene Therapy to Target LAMA2 for Congenital Muscular Dystrophy – Drug Profile
GNT-0008 – Drug Profile
IP-300W – Drug Profile
IUCT-169 – Drug Profile
IUCT-290 – Drug Profile
IUCT-309 – Drug Profile
JM-642 – Drug Profile
JUV-161 – Drug Profile
KER-050 – Drug Profile
ketoprofen – Drug Profile
LGMD2B – Drug Profile
LION-101 – Drug Profile
losmapimod – Drug Profile
LR-08 – Drug Profile
LUB-002 – Drug Profile
MCDX-4 – Drug Profile
MD-1 – Drug Profile
MDL-101 – Drug Profile
mexiletine hydrochloride – Drug Profile
Myotonic Dystrophy Type 1 – Drug Profile
N/D FSHD – Drug Profile
nandrolone decanoate – Drug Profile
Next-Generation Research Programs – Drug Profile
NS-035 – Drug Profile
NT-0200 – Drug Profile
NT-0231.F – Drug Profile
PDA-002 – Drug Profile
PGN-EDODM1 – Drug Profile
pitolisant hydrochloride – Drug Profile
poloxamer – Drug Profile
rebastinib – Drug Profile
RG-6237 – Drug Profile
RHLAM-111 – Drug Profile
ribitol – Drug Profile
RNAi Gene Therapy to Inhibit DUX4 for Facioscapulohumeral Muscular Dystrophy – Drug Profile
RNAi Gene Therapy to Inhibit Myotilin for LGMD – Drug Profile
RP-33 – Drug Profile
SB-308 – Drug Profile
SIWA-318 – Drug Profile
Small Molecule for Algodystrophy, Chemotherapy Induced Peripheral Neuropathy, Diabetic Peripheral Neuropathy and Pain – Drug Profile
Small Molecule to Inhibit DMPK for Myotonic Dystrophy – Drug Profile
Small Molecule to Target CUG RNA for Myotonic Dystrophy 1 – Drug Profile
Small Molecule to Target RNA for Myotonic Dystrophy Type 1 – Drug Profile
Small Molecules for Emery-Dreifuss Muscular Dystrophy – Drug Profile
Small Molecules for Huntington Disease, Genetic Disorders and Myotonic Dystrophy – Drug Profile
Small Molecules for Laminin-Deficient Congenital Muscular Dystrophy – Drug Profile
Small Molecules for Muscular Dystrophy – Drug Profile
Small Molecules for Myotonic Dystrophy – Drug Profile
Small Molecules for Myotonic Dystrophy Type 2 – Drug Profile
Small Molecules to Activate AMPK for Glomerulonephritis, Polycystic Kidney Disease, Myotonic Dystrophy and Mitochondrial Diseases – Drug Profile
Small Molecules to Activate FKRP for Limb-Girdle Muscular Dystrophy – Drug Profile
Small Molecules to Activate SMCHD1 for Facioscapulohumeral Muscular Dystrophy – Drug Profile
Small Molecules to Agonize CB1 and CB2 for Myotonic Dystrophy and Myotonia – Drug Profile
Small Molecules to Agonize TRPML1 for Muscular Dystrophy – Drug Profile
Small Molecules to Inhibit CNBP for Myotonic Dystrophy Type 2 – Drug Profile
Small Molecules to Inhibit DMPK for Myotonic Dystrophy Type 1 – Drug Profile
Small Molecules to Target RNA for Myotonic Dystrophy – Drug Profile
SRP-6004 – Drug Profile
SRP-9003 – Drug Profile
SRP-9004 – Drug Profile
SRP-9005 – Drug Profile
SRP-9006 – Drug Profile
Synthetic Peptides to Inhibit Tcp for Neurodegenerative Disorders, Muscular Dystrophy and Oncology – Drug Profile
tideglusib – Drug Profile
trehalose – Drug Profile
tRNA Enzyme Pairs – Drug Profile
TTX-3360 – Drug Profile
TXA-127 – Drug Profile
vamorolone – Drug Profile
VTA-100 – Drug Profile
VTA-120 – Drug Profile
VTA-200 – Drug Profile
XN-001 – Drug Profile
Muscular Dystrophy – Dormant Projects
Muscular Dystrophy – Discontinued Products
Muscular Dystrophy – Product Development Milestones
Featured News & Press Releases
Oct 14, 2022: Avidity Biosciences announces upcoming presentation on AOC-1001 at 27th International Hybrid Annual Congress of World Muscle Society
Sep 28, 2022: FDA places partial hold on Avidity’s Phase I/II myotonic dystrophy trial
Sep 27, 2022: Atamyo doses first subject in Phase I/II muscular dystrophy therapy trial
Aug 04, 2022: Entrada Therapeutics announces collaboration with the Myotonic Dystrophy Clinical Research Network to study the natural history of myotonic dystrophy type 1
Aug 02, 2022: Avidity Biosciences enrolls patients in the MARINA open-label extension study
Jul 13, 2022: Fulcrum phase 3 FSHD clinical trial using AMRA Medical's Whole-body MRI Measurements as a Key Secondary Endpoint
Jul 12, 2022: Dyne Therapeutics announces clearance of clinical trial application for DYNE-101 for the treatment of myotonic dystrophy type 1
Jul 05, 2022: Fulcrum Therapeutics enrolls first patient in pivotal global Phase 3 clinical trial of Losmapimod for facioscapulohumeral muscular dystrophy (FSHD)
Jun 20, 2022: New muscle disease indication for ATL1102 – Limb girdle muscular dystrophy R2
May 17, 2022: NeuBase presents new preclinical data at ASGCT 2022 for its DM1 program demonstrating wide tissue distribution and supporting a differentiated whole-body treatment solution
May 16, 2022: Dyne Therapeutics presents new in vivo data from DYNE-101 at ASGCT Annual Meeting demonstrating low monthly dosing leads to robust DMPK RNA knockdown
May 16, 2022: Atamyo Therapeutics announces significant for ATA-100 to treat Limb-Girdle Muscular Dystrophy 2I/R9
May 11, 2022: Entrada Therapeutics presents new data supporting its growing pipeline of Endosomal Escape Vehicle (EEV™) therapeutics, including ENTR-701 at TIDES USA 2022
May 02, 2022: NeuBase Therapeutics announces presentations at the American Society of Gene & Cell Therapy (ASGCT) 2022 Annual Meeting
Appendix
Methodology
Coverage
Secondary Research
Primary Research
Expert Panel Validation
Contact Us
Disclaimer
List of Tables
Table 1: Number of Products under Development for Muscular Dystrophy, 2022
Table 2: Number of Products under Development by Companies, 2022
Table 3: Number of Products under Development by Companies, 2022 (Contd..1)
Table 4: Number of Products under Development by Companies, 2022 (Contd..2)
Table 5: Number of Products under Development by Companies, 2022 (Contd..3)
Table 6: Number of Products under Development by Universities/Institutes, 2022
Table 7: Products under Development by Companies, 2022
Table 8: Products under Development by Companies, 2022 (Contd..1)
Table 9: Products under Development by Companies, 2022 (Contd..2)
Table 10: Products under Development by Companies, 2022 (Contd..3)
Table 11: Products under Development by Companies, 2022 (Contd..4)
Table 12: Products under Development by Companies, 2022 (Contd..5)
Table 13: Products under Development by Companies, 2022 (Contd..6)
Table 14: Products under Development by Universities/Institutes, 2022
Table 15: Number of Products by Stage and Target, 2022
Table 16: Number of Products by Stage and Target, 2022 (Contd..1)
Table 17: Number of Products by Stage and Mechanism of Action, 2022
Table 18: Number of Products by Stage and Mechanism of Action, 2022 (Contd..1)
Table 19: Number of Products by Stage and Route of Administration, 2022
Table 20: Number of Products by Stage and Molecule Type, 2022
Table 21: Muscular Dystrophy – Pipeline by Achelios Therapeutics Inc, 2022
Table 22: Muscular Dystrophy – Pipeline by Altay Therapeutics Inc, 2022
Table 23: Muscular Dystrophy – Pipeline by Amicus Therapeutics Inc, 2022
Table 24: Muscular Dystrophy – Pipeline by AMO Pharma Ltd, 2022
Table 25: Muscular Dystrophy – Pipeline by Anima Biotech Inc, 2022
Table 26: Muscular Dystrophy – Pipeline by Antisense Therapeutics Ltd, 2022
Table 27: Muscular Dystrophy – Pipeline by ARMGO Pharma Inc, 2022
Table 28: Muscular Dystrophy – Pipeline by Arrowhead Pharmaceuticals Inc, 2022
Table 29: Muscular Dystrophy – Pipeline by ARTHEx Biotech SL, 2022
Table 30: Muscular Dystrophy – Pipeline by Asklepios BioPharmaceutical Inc, 2022
Table 31: Muscular Dystrophy – Pipeline by Astellas Gene Therapies, 2022
Table 32: Muscular Dystrophy – Pipeline by Atamyo Therapeutics SAS, 2022
Table 33: Muscular Dystrophy – Pipeline by Avidity Biosciences Inc, 2022
Table 34: Muscular Dystrophy – Pipeline by Beech Tree Labs Inc, 2022
Table 35: Muscular Dystrophy – Pipeline by Benitec Biopharma Inc, 2022
Table 36: Muscular Dystrophy – Pipeline by Biophytis SA, 2022
Table 37: Muscular Dystrophy – Pipeline by Bioprojet SCR, 2022
Table 38: Muscular Dystrophy – Pipeline by CalyGene Biotechnology Inc, 2022
Table 39: Muscular Dystrophy – Pipeline by CANbridge Life Sciences Ltd, 2022
Table 40: Muscular Dystrophy – Pipeline by Casma Therapeutics Inc, 2022
Table 41: Muscular Dystrophy – Pipeline by Celularity Inc, 2022
Table 42: Muscular Dystrophy – Pipeline by Chugai Pharmaceutical Co Ltd, 2022
Table 43: Muscular Dystrophy – Pipeline by Constant Therapeutics LLC, 2022
Table 44: Muscular Dystrophy – Pipeline by CRISPR Therapeutics AG, 2022
Table 45: Muscular Dystrophy – Pipeline by Debiopharm International SA, 2022
Table 46: Muscular Dystrophy – Pipeline by Design Therapeutics Inc, 2022
Table 47: Muscular Dystrophy – Pipeline by DR.Noah Biotech Inc, 2022
Table 48: Muscular Dystrophy – Pipeline by Dyne Therapeutics Inc, 2022
Table 49: Muscular Dystrophy – Pipeline by Edgewise Therapeutics Inc, 2022
Table 50: Muscular Dystrophy – Pipeline by Elixirgen Therapeutics Inc, 2022
Table 51: Muscular Dystrophy – Pipeline by Entrada Therapeutics Inc, 2022
Table 52: Muscular Dystrophy – Pipeline by Enzerna Biosciences LLC, 2022
Table 53: Muscular Dystrophy – Pipeline by Epicrispr Biotechnologies Inc, 2022
Table 54: Muscular Dystrophy – Pipeline by EpiSwitch Rx Inc, 2022
Table 55: Muscular Dystrophy – Pipeline by Exodos Life Sciences Limited Partnership, 2022
Table 56: Muscular Dystrophy – Pipeline by Expansion Therapeutics Inc, 2022
Table 57: Muscular Dystrophy – Pipeline by F. Hoffmann-La Roche Ltd, 2022
Table 58: Muscular Dystrophy – Pipeline by Facio Therapies BV, 2022
Table 59: Muscular Dystrophy – Pipeline by Faze medicines, 2022
Table 60: Muscular Dystrophy – Pipeline by Fulcrum Therapeutics Inc, 2022
Table 61: Muscular Dystrophy – Pipeline by Generian Pharmaceuticals Inc, 2022
Table 62: Muscular Dystrophy – Pipeline by Healx Ltd, 2022
Table 63: Muscular Dystrophy – Pipeline by Hope Biosciences LLC, 2022
Table 64: Muscular Dystrophy – Pipeline by Juvena Therapeutics Inc, 2022
Table 65: Muscular Dystrophy – Pipeline by Keros Therapeutics Inc, 2022
Table 66: Muscular Dystrophy – Pipeline by LinkedUp Bioscience Inc, 2022
Table 67: Muscular Dystrophy – Pipeline by Locanabio Inc, 2022
Table 68: Muscular Dystrophy – Pipeline by Loqus23 Therapeutics Ltd, 2022
Table 69: Muscular Dystrophy – Pipeline by Lupin Ltd, 2022
Table 70: Muscular Dystrophy – Pipeline by ML Bio Solutions Inc, 2022
Table 71: Muscular Dystrophy – Pipeline by Modalis Therapeutics Corp, 2022
Table 72: Muscular Dystrophy – Pipeline by Myocea Inc, 2022
Table 73: Muscular Dystrophy – Pipeline by Myogem Health Company SL, 2022
Table 74: Muscular Dystrophy – Pipeline by NeuBase Therapeutics Inc, 2022
Table 75: Muscular Dystrophy – Pipeline by Nexien Biopharma Inc, 2022
Table 76: Muscular Dystrophy – Pipeline by Nippon Shinyaku Co Ltd, 2022
Table 77: Muscular Dystrophy – Pipeline by Nymirum Inc, 2022
Table 78: Muscular Dystrophy – Pipeline by Pasithea Therapeutics Corp, 2022
Table 79: Muscular Dystrophy – Pipeline by Pepgen Inc, 2022
Table 80: Muscular Dystrophy – Pipeline by Pfizer Inc, 2022
Table 81: Muscular Dystrophy – Pipeline by Phrixus Pharmaceuticals Inc, 2022
Table 82: Muscular Dystrophy – Pipeline by Prothelia Inc, 2022
Table 83: Muscular Dystrophy – Pipeline by QiXia Decode Therapeutics, 2022
Table 84: Muscular Dystrophy – Pipeline by Recursion Pharmaceuticals Inc, 2022
Table 85: Muscular Dystrophy – Pipeline by SanBio Co Ltd, 2022
Table 86: Muscular Dystrophy – Pipeline by Sanofi, 2022
Table 87: Muscular Dystrophy – Pipeline by Santhera Pharmaceuticals Holding AG, 2022
Table 88: Muscular Dystrophy – Pipeline by Sarcomed AB, 2022
Table 89: Muscular Dystrophy – Pipeline by Sarepta Therapeutics Inc, 2022
Table 90: Muscular Dystrophy – Pipeline by Scriptr Global Inc, 2022
Table 91: Muscular Dystrophy – Pipeline by SEAL Therapeutics AG, 2022
Table 92: Muscular Dystrophy – Pipeline by Seelos Therapeutics, Inc., 2022
Table 93: Muscular Dystrophy – Pipeline by Siwa Therapeutics Inc, 2022
Table 94: Muscular Dystrophy – Pipeline by Syros Pharmaceuticals Inc, 2022
Table 95: Muscular Dystrophy – Pipeline by Triplet Therapeutics Inc, 2022
Table 96: Muscular Dystrophy – Pipeline by Vertex Pharmaceuticals Inc, 2022
Table 97: Muscular Dystrophy – Pipeline by Vita Therapeutics Inc, 2022
Table 98: Muscular Dystrophy – Pipeline by Xonovo Inc, 2022
Table 99: Muscular Dystrophy – Dormant Projects, 2022
Table 100: Muscular Dystrophy – Dormant Projects, 2022 (Contd..1)
Table 101: Muscular Dystrophy – Dormant Projects, 2022 (Contd..2)
Table 102: Muscular Dystrophy – Dormant Projects, 2022 (Contd..3)
Table 103: Muscular Dystrophy – Discontinued Products, 2022
List of Figures
Figure 1: Number of Products under Development for Muscular Dystrophy, 2022
Figure 2: Number of Products under Development by Companies, 2022
Figure 3: Number of Products under Development by Universities/Institutes, 2022
Figure 4: Number of Products by Top 10 Targets, 2022
Figure 5: Number of Products by Stage and Top 10 Targets, 2022
Figure 6: Number of Products by Top 10 Mechanism of Actions, 2022
Figure 7: Number of Products by Stage and Top 10 Mechanism of Actions, 2022
Figure 8: Number of Products by Routes of Administration, 2022
Figure 9: Number of Products by Stage and Routes of Administration, 2022
Figure 10: Number of Products by Top 10 Molecule Types, 2022
Figure 11: Number of Products by Stage and Top 10 Molecule Types, 2022

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