Roots Analysis
To order this 640+
page report, which features 235+ figures and 275+ tables, please visit this - https://www.rootsanalysis.com/reports/view_document/human-microbiome-market/281.html
Key Market Insights
§
§
§
§
§
§
§
§
§
§
For
more information please visit:
https://www.rootsanalysis.com/reports/view_document/human-microbiome-market/281.html
Table of Contents
1. PREFACE
1.1. Scope of the Report
1.2. Research Methodology
1.3. Chapter Outlines
2. EXECUTIVE SUMMARY
3. INTRODUCTION
3.1. Chapter Overview
3.2. Concept of Microbiota and Microbiome
3.2.1. Discovery of the Human Microbiome
3.2.2. Functions of the Human Microbiome
3.3. Overview of Gut Flora
3.3.1. Role of Gut Flora in Healthy Individuals
3.3.2. Factors Affecting Gut Flora
3.3.2.1. Antibiotic Consumption
3.3.2.2. Age and Pregnancy
3.3.2.2.1. Mode of
Childbirth
3.3.2.2.2. Type of
Feeding
3.3.2.2.3. Antibiotic
Consumption by Mother
3.3.2.3. Stress-related Factors
3.3.2.4. Dietary Factors
3.3.2.5. Impact of Lifestyle
3.4. The Microbiome and Disease
3.4.1. Cancer
3.4.2. Inflammatory Bowel Disease (IBD)
3.4.3. Obesity
3.4.4. Parkinson’s Disease
3.4.5. Type-II Diabetes
3.4.6. Other Disease Indications
3.5. Impact of Microbiota on Drug
Pharmacokinetics
3.6. Impact of Microbiota on Therapeutic
Outcomes
3.7. Microbiome Therapeutics
3.7.1. Probiotics
3.7.1.1. Beneficial Bacterial Strains
3.7.1.1.1. Lactobacilli
3.7.1.1.2. Bifidobacteria
3.7.1.1.3. Others
3.7.1.2. Key Therapeutic Areas
3.7.1.2.1. Antibiotic-Associated
Diarrhea (AAD)
3.7.1.2.2. Bacterial
Vaginosis
3.7.1.2.3. High Blood
Pressure
3.7.1.2.4. Hypercholesterolemia
3.7.1.2.5. Infectious
Childhood Diarrhea (ICD)
3.7.1.2.6. Inflammatory
Bowel Disease (IBD)
3.7.1.2.7. Lactose
Intolerance
3.7.1.2.8. Vitamin
Production
3.7.1.2.9. Weight
Management
3.7.1.3. Side Effects of Probiotics
3.7.2. Prebiotics
3.7.2.1. Sources of Prebiotics
3.7.2.2. Types of Prebiotics
3.7.2.2.1. Fructo-Oligosaccharides
(FOS)
3.7.2.2.2. Galacto-Oligosaccharides
(GOS)
3.7.2.2.3. Inulin
3.7.2.3. Key Therapeutic Areas
3.7.2.3.1. Antibiotic
Associated Diarrhea (AAD)
3.7.2.3.2. Constipation
3.7.2.3.3. Gastrointestinal
Disorders
3.7.2.3.4. Dysbiosis
3.7.2.4. Side Effects of Prebiotics
3.8. The Human Microbiome Project (HMP)
3.8.1. Project Approach
3.8.2. Project Initiatives
3.8.3. Project Achievements
3.9. Regulatory Guidelines for Live
Biotherapeutic Products (LBPs)
3.10. Key Challenges in the Development of
Microbiome Therapeutics
3.11. Future Perspectives
4. MICROBIOME THERAPEUTICS:
MARKET LANDSCAPE
4.1. Chapter Overview
4.2. Microbiome Therapeutics: Clinical
Pipeline
4.2.1. Analysis by Phase of Development
4.2.2. Analysis by Type of Molecule
4.2.3. Analysis by Type of Therapy
4.2.4. Analysis by Target Indication
4.2.5. Analysis by Therapeutic Area
4.2.6. Analysis by Dosing Frequency
4.2.7. Analysis by Route of Administration
4.2.8. Analysis by Drug Formulation
4.3. Microbiome Therapeutics: Early-Stage
Pipeline
4.3.1. Analysis by Phase of Development
4.3.2. Analysis by Type of Molecule
4.3.3. Analysis by Type of Therapy
4.3.4. Analysis by Target Indication
4.3.5. Analysis by Therapeutic Area
4.4. Microbiome Therapeutics: List of Drug
Developers
4.4.1. Analysis by Year of Establishment
4.4.2. Analysis by Location of Headquarters
4.4.3. Analysis by Company Size
4.4.4. Analysis by Company Size and Location of
Headquarters
4.4.5. Leading Drug Developers: Analysis by Number
of Microbiome Therapeutics
4.5. Grid Analysis: Microbiome and Key
Therapeutic Areas
4.6. Microbiome Therapeutics: List of
Discontinued Drugs
4.7. Emerging Role of Microbiome in Gut-Brain
Axis
4.8. Microbiome Therapeutics: List of
Technology Platforms
5. COMPANY AND DRUG
PROFILES
5.1. Chapter Overview
5.2. 4D Pharma
5.2.1. Company Overview
5.2.2. Microbiome-based Product Portfolio
5.2.2.1. Blautix®
5.2.2.1.1. Drug
Overview
5.2.2.1.2. Current
Status of Development
5.2.2.1.3. Clinical
Studies
5.2.2.1.4. Clinical
Trial End-Point Analysis
5.2.3. Recent Developments and Future Outlook
5.3. Armata Pharmaceuticals
5.3.1. Company Overview
5.3.2. Microbiome-Based Product Portfolio
5.3.2.1. C16G2
5.3.2.1.1. Drug
Overview
5.3.2.1.2. Current
Status of Development
5.3.2.1.3. Clinical
Studies
5.3.2.1.4. Clinical
Trial End-Point Analysis
5.3.3. Recent Developments and Future Outlook
5.4. Evelo Biosciences
5.4.1. Company Overview
5.4.2. Microbiome-Based Product Portfolio
5.4.2.1. EDP1503
5.4.2.1.1. Drug
Overview
5.4.2.1.2. Current
Status of Development
5.4.2.1.3. Clinical
Studies
5.4.2.1.4. Clinical
Trial End-Point Analysis
5.4.3. Recent Developments and Future Outlook
5.5. Rebiotix (Acquired by Ferring
Pharmaceuticals)
5.5.1. Company Overview
5.5.2. Financial Information
5.5.3. Microbiome-Based Product Portfolio
5.5.3.1. RBX2660
5.5.3.1.1. Drug
Overview
5.5.3.1.2. Current
Status of Development
5.5.3.1.3. Clinical
Studies
5.5.3.1.4. Clinical
Trial End-Point Analysis
5.5.4. Recent Developments and Future Outlook
5.6. Seres Therapeutics
5.6.1. Company Overview
5.6.2. Financial Information
5.6.3. Microbiome-Based Product Portfolio
5.6.3.1. SER-109
5.6.3.1.1. Drug
Overview
5.6.3.1.2. Current
Status of Development
5.6.3.1.3. Clinical
Studies
5.6.3.1.4. Clinical
Trial End-Point Analysis
5.6.3.2. SER-287
5.6.3.2.1. Current
Status of Development
5.6.3.2.3. Clinical
Studies
5.6.3.2.4. Clinical
Trial End-Point Analysis
5.6.4. Recent Developments and Future Outlook
5.7. Vedanta Biosciences
5.7.1. Company Overview
5.7.2. Microbiome-Based Product Portfolio
5.7.2.1. VE303
5.7.2.1.1. Drug
Overview
5.7.2.1.2. Current
Status of Development
5.7.2.1.3. Clinical
Studies
5.7.3.1.4. Clinical
Trial End-Point Analysis
5.7.3. Recent Developments and Future Outlook
6. MICROBIOME DIAGNOSTICS:
MARKET LANDSCAPE
6.1. Chapter Overview
6.2. Overview of Microbiome Diagnostic Tests
6.3. Microbiome Diagnostic Tests: Marketed and
Under Development Products
6.3.1. Analysis by Stage of Development
6.3.2. Analysis by Type of Sample Required
6.3.3. Analysis by Target Indication
6.3.4. Analysis by Therapeutic Area
6.3.5. Analysis by Purpose
6.4. Microbiome Diagnostic Tests: List of
Diagnostic Developers
6.4.1. Analysis by Year of Establishment
6.4.2. Analysis by Location of
Headquarters
6.4.3. Analysis by Company Size
6.4.4. Analysis by Company Size and Location of
Headquarters
6.4.5. Leading Diagnostic Developers: Analysis by
Number of Microbiome Diagnostics
6.5. Profiles of Prominent Diagnostic
Developers
6.5.1. Enterome Bioscience
6.5.1.1. Company Overview
6.5.1.2. Service Portfolio
6.5.2. Vaiomer
6.5.2.1. Company Overview
6.5.2.2. Service Portfolio
6.6. Overview of Microbiome Screening /
Profiling Tests
6.6.1. List of Microbiome Screening / Profiling
Tests
6.6.2. List of Microbiome Screening / Profiling
Test Developers
7. FECAL MICROBIOTA THERAPY
(FMT)
7.1. Chapter Overview
7.2. Introduction to FMT
7.3. Historical Overview
7.4. FMT: Procedure and Clinical Relevance
7.4.1. Donor Selection
7.4.2. Administration Procedure
7.4.3. Routes of Administration
7.4.4. Consequences and Adverse Events
7.4.5. Clinical Guidelines Associated with FMT
7.5. Regulatory Guidelines Related to FMT
7.6. Insurance Coverage for FMT
7.7. FMT: Competitive Landscape
7.7.1. Marketed / Development Pipeline (Industry
Players)
7.7.1.1. Analysis by Phase of Development
7.7.1.2. Analysis by Therapeutic Area
7.7.1.3. Analysis by Route of Administration
7.7.2. List of Developers (Industry Players)
7.7.2.1. Analysis by Year of Establishment
7.7.2.2. Analysis by Location of Headquarters
7.7.2.3. Analysis by Company Size
7.8. Clinical Trial Analysis (Non-Industry
Sponsored)
7.8.1. Scope and Methodology
7.8.2. List of Clinical Trials
7.8.2.1. Analysis by Trial Registration Year
7.8.2.2. Analysis by Trial Status
7.8.2.3. Analysis by Phase of Development
7.8.2.4. Analysis by Patients Enrolled
7.8.2.5. Analysis of Number of Patients Enrolled by
Trial Registration Year
7.8.2.6. Analysis by Therapeutic Area
7.8.2.7. Analysis by Popular Target Indications
7.8.2.8. Analysis by Trial Registration Year and
Recruitment Status
7.8.2.9. Analysis by Study Design
7.8.2.10. Leading Non-Industry Players:
Analysis by Number of Trials
7.8.2.11. Geographical Analysis by Number of
Clinical Trials
7.8.2.12. Geographical Analysis by Enrolled
Patient Population
7.8.2.13. Analysis by Type of Sponsor / Collaborator
7.8.2.14. Analysis by Trial Focus
7.8.2.15. Key Clinical Trials
7.9. Stool Banks
7.9.1. Introduction to Stool Banks
7.9.2. List of Stool Banks
7.9.3. Profiles of Prominent Stool Banks
7.9.3.1. AdvancingBio
7.9.3.1.1. Overview
7.9.3.1.2. Fecal Microbiota
Preparation
7.9.3.2. Asia Microbiota bank
7.9.3.2.1. Overview
7.9.3.2.2. Fecal
Microbiota Preparation
7.9.3.3. Enterobiotix
7.9.3.3.1. Overview
7.9.3.3.2. Fecal
Microbiota Preparation
7.9.3.4. Flora Medicine
7.9.3.4.1. Overview
7.9.3.4.2. Fecal
Microbiota Preparation
7.9.3.5. OpenBiome
7.9.3.5.1. Overview
7.9.3.5.2. Fecal
Microbiota Preparation
8. ATTRACTIVENESS
COMPETITIVENESS (AC) MATRIX
8.1. Chapter Overview
8.2. AC Matrix: An Overview
8.2.1. Strong Opportunity Areas
8.2.2. Average Opportunity Areas
8.2.3. Weak Opportunity Areas
8.3. AC Matrix: Analytical Methodology
8.4. AC Matrix: Plotting the Information
8.5. AC Matrix: Analyzing the Data
8.5.1. Strong Opportunity Areas
8.5.2. Average Opportunity Areas
8.5.3. Weak Opportunity Areas
Contact Details
Gaurav
Chaudhary
+1
(415) 800 3415
