Human Microbiome-based Products Market is projected to be worth USD 4 Billion by 2030

Roots Analysis has announced the addition of “Human Microbiome Market, 2019-2030” report to its list of offerings.

The concept of microbiome-based therapeutics has generated significant enthusiasm within the medical science community, defining a new frontier in the field of medicine. Despite having captured the interest of several venture capital firms and big pharma players, no microbiome-based therapeutic has been officially approved by an authorized medical product regulator. However, the current development pipeline of microbiome therapeutics has several promising candidates that are likely to result in commercial success stories soon.

Key Market Insights

260 therapy candidates are currently in different phases of development

Nearly 25% of pipeline drugs are in the clinical phase of development, while the rest are in the preclinical / discovery stage. Interestingly, most of these drugs target digestive and gastrointestinal disorders (20%); this is followed by product candidates intended for treatment of oncological disorders (17%) and infectious diseases (13%).

Over 30 microbiome diagnostic tests are currently available / under development

Around 30% of the abovementioned tests have been commercialized, while the rest are under development. Of the total tests, notable examples of companies that launched a microbiome-based diagnostic solution include (in alphabetical order) ARTPred, Genetic Analysis, Goodgut, Invivo Healthcare, IS-diagnostics, Luxia Scientific and Varinos.

FMTs are the only commercially available microbiome therapy

This therapeutic product is presently indicated for the treatment of recurrent Clostridium difficile infections (rCDIs). Further, non-industry players (such as University of Alberta, The Second Hospital of Nanjing Medical University, University of California and Chinese University of Hong Kong) are making notable contributions in this arena, having been involved in ~200 clinical trials till August 2019.

51% growth in capital investments has been observed since 2015; around 70% investment has come from Venture Capital investors

It is worth noting that more than 80 investors have supported the RD programs initiated by start-ups focused on microbiome-related products. Well-funded start-ups have initiated product development programs, having invested significant time and effort to explore the applicability of microbiome therapeutics across various indications.

North America and Europe are anticipated to capture over 85% of the market share by 2030

As late stage products are commercialized, the microbiome therapeutics market is likely to grow at an annualized growth rate of over 30%, during the next decade. In addition to North America and Europe, the market in China / broader Asia Pacific region is also anticipated to grow at a relatively faster rate.

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Key Questions Answered

Who are the leading developers of microbiome therapeutics and diagnostic tests?
What are the key technology platforms (available / under development) for microbiome-related therapies and diagnostics?
What are the disease indications against which microbiome-based therapeutics are being evaluated?
Which companies are targeting gut-brain axis for the development of microbiome therapies?
Who are the leading (industry and non-industry) players involved in the development of FMT products?
Who are the key contract research / manufacturing service providers in this domain?
What is the trend in capital investments in microbiome-related RD?
What are the contributions of big pharma players in this domain?
Which are the popular players offering big data-related services / tools to support microbiome research?
How is the current and future market opportunity for microbiome-based therapeutics and diagnostics is likely to be distributed across key market segments?

The USD 4 billion (by 2030) financial opportunity within the microbiome therapeutics (Tx) market and diagnostics (Dx) markets, has been analyzed across the following segments:

Type of Therapy (Tx)
Prescription Drug
Prebiotics
Probiotics

Type of Molecule (Tx)
Small Molecules
Biologics

Target Indication (Tx+Dx)
Acne Vulgaris
Atopic Dermatitis
Clostridium difficile Infection
Colorectal Cancer
Crohn’s Disease
Diabetes
Irritable Bowel Syndrome
Lactose Intolerance
Lung Cancer
Nonalcoholic steatohepatitis (NASH)
Obesity
Ulcerative colitis

Therapeutic Area (Tx+Dx)
Autoimmune Disorders
Dental Disorders
Digestive and Gastrointestinal Disorders
Dermatological Disorders
Infectious Disease
Metabolic Disorders
Oncology
Others

Key Geographical Regions (Tx+Dx)
North America
Europe
Asia-Pacific and Rest of the World

The report features inputs from eminent industry stakeholders, according to whom innovation in microbiome-related research is mostly being driven by start-ups / small-sized companies. The report includes detailed transcripts of discussions held with the following experts:

Veronika Oudova (Co-founder and Chief Executive Officer, S-Biomedic)
Colleen Cutcliffe (Co-founder and Chief Executive Officer, Whole Biome)
Lee Jones (President and Chief Executive Officer, Rebiotix)
Mark Heiman (Chief Scientific Officer and Vice President, Research, MicroBiome Therapeutics)
Assaf Oron (Chief Business Officer, BiomX)
Pierre-Alain Bandinelli (Chief Business Officer, Da Volterra)
Nikole E Kimes (Co-founder and Vice President, Siolta Therapeutics)
James Burges (Executive Director, OpenBiome)
JP Benya (Vice President, Business Development, Assembly Biosciences)
Debbie Pinkston (Vice President, Sales and Business Development, List Biological Laboratories)
Gregory J Kuehn (Vice President, Business Development and Marketing, Metabiomics)
Alexander Segal (Vice President, Business Development, Universal Stabilization Technologies)
Alexander Lin (Associate General Manager, Chung Mei Pharmaceutical)
Aaron Wright (Senior Scientist, Pacific Northwest National Laboratories)

The research covers detailed profiles, featuring a brief company overview, its financial information (if available), product portfolio details (such as status of development of pipeline candidates, clinical trial information and analysis of key trial end-points), recent developments and an informed future outlook.