ADM unpacks postbiotics and strain-specific microbiome clinical trials
Key takeaways
- ADM underscores the importance of strain-specific clinical research as efficacy can’t be generalized across genus or species.
- Research on postbiotics finds that these inactivated microorganisms deliver comparable trial results as live strains, with formulation and stability advantages.
- ADM says preclinical and clinical research are key in gut microbiome science, although it can be challenging for regulations to match the pace of research.

Expanding research on the gut microbiome and its connections to other health areas is driving product development in the nutrition industry. ADM says advances in women’s health metabolites, the gut-brain axis, and strain-specific clinical research are helping companies develop more targeted, evidence-based solutions.
Nutrition Insight discusses microbiome breakthroughs and clinical research with Dr. Malwina Naghibi, head of Clinical Development in ADM’s R&D Medical Team.
“Some of the most significant breakthroughs have been expanding our understanding of how the microbiome interacts with the human body, new insights into mother-baby interactions, and a growing recognition of the role that microbial metabolites and postbiotics play in supporting health.”
She says that these advances are already beginning to influence clinical practice and product development with tangible impacts on people’s health and well-being.
Moreover, Naghibi points to the potential benefit of microbiome modulation prior to, or alongside, pharmacological treatments as an important area of progress.
“For example, a King’s College London, UK, study explored the effects of an ADM probiotic in 49 patients with clinical depression. Study results suggest adjunctive microbiome solutions — in this case, a probiotic — may improve mood compared to the placebo group, although larger confirmatory studies are still needed.”
Women’s health breakthroughs
Naghibi notes that research has expanded the understanding of the microbiome connection between mothers and babies. “We know now that even if twins are born with the same genetic material, their microbiome footprint can be different within days of birth, influenced by factors such as order of birth and gestational age.”
As key breakthroughs, Naghibi points to growing knowledge of microbiome interactions with the body, new insights on mother-baby interactions, and the role of postbiotics (Image credit: ADM).“A 2025 publication in Nature Medicine significantly advanced our understanding of how we see environmental mechanisms shaping a baby’s microbiome in their early days and into childhood.”
In this 2025 study, researchers mapped the gut microbiome evolution in twins, from birth until they were eight years old.
“We also now have evidence to guide us deeper into understanding the role of how a Lactobacillus-dominated vaginal microbiome can influence healthy pregnancies,” adds Naghibi. “In contrast to the gut microbiome, lower microbial diversity (with a dominance of Lactobacillus species) is generally associated with vaginal health.”
Harnessing postbiotics
Naghibi says another major shift has been moving beyond identifying which microbes are present to understanding what they are actually doing.
“Today, researchers are increasingly focused on microbial metabolites — the bioactive compounds produced by the microbiome, such as short-chain fatty acids, bile acids, and tryptophan metabolites — which are now recognized as key drivers of microbiome function.”
She explains that this shift has also accelerated interest in postbiotics, where inactivated microorganisms may deliver health benefits with advantages in stability, formulation, and manufacturing compared with live microbes.
“ADM is investing significantly in preclinical and clinical research in postbiotics, across a range of physiologies.”
“Two ADM trials have helped reshape our understanding of postbiotics,” Naghibi details. “In an irritable bowel syndrome clinical trial published in 2024, a probiotic and a postbiotic of the same Bifidobacterium longum CECT7347 strain (Esflorin1) generated comparable results, offering significant improvement in symptom scores and quality of life.”
Additionally, she says a second clinical trial in allergic rhinitis reported clinically meaningful improvements for individuals in the postbiotic group, compared to placebo control.
Gut-brain axis
Naghibi points to the gut-brain axis and psychobiotics as some of the “most exciting areas of innovation.”
Research has found that even if twins are born with the same genetic material, their microbiome footprint can be different within days of birth.“The growing prevalence of anxiety, depression, stress, and other mental well-being challenges, particularly among adolescents and young adults, highlights the need for innovative approaches like biotic solutions that can support overall health and wellness.”
“As our understanding of the connection between the gut microbiome and cognitive and emotional well-being continues to evolve, biotic solutions have incredible innovation potential to complement broader wellness strategies and support the mental health of current and future generations.”
Nutrition Insight recently explored how the gut-brain axis and botanicals fuel next-generation sleep and stress supplements. Ingredient suppliers said that clinical science, probiotics, botanical extracts, and multifunctional ingredients are reshaping supplements through systems-level support.
Pipeline standards
ADM’s preclinical and clinical pipeline aims to achieve tangible effects for individual consumers. The company has set up R&D centers in Valencia (Spain), Kennesaw (US), Cork (Ireland), and Wuxi (China).
Naghibi notes these work on multiple biotics and numerous preclinical evaluations at any given time to inform decisions on the best candidate biotics to take forward to human clinical trials.
“One of the field’s most important learnings is that efficacy cannot be generalized across a bacterial genus or species. Rather, effects are strain-specific. Clinical evidence needs to be generated for individual strains or well-characterized strain combinations, making rigorous preclinical work essential.”
She adds that, historically, many probiotic products entered clinical testing without extensive mechanistic characterization. “At ADM, we begin by thoroughly characterizing candidate strains, including full genome sequencing and safety assessments, before evaluating their stability and biological activity in a range of preclinical models.”
“If data are promising, we then advance to human clinical trials,” Naghibi explains. “ADM’s R&D Medical Team helps translate those results into relevant, scientifically rigorous clinical trials.”
“We believe the industry should hold itself to the highest standards of clinical evidence, which includes well-designed, randomized, controlled clinical trials following the standards of Good Clinical Practice (GCP).”
Because effects are strain-specific, Naghibi says rigorous preclinical work is essential to generate evidence for individual strains or combinations.She underscores that this level of scientific rigor is essential for building a reliable, reproducible, scientifically sound body of evidence, earning consumer trust, and moving the microbiome field forward.
“That’s why all 25 clinical trials currently in ADM’s pipeline are randomized, double-blind, placebo-controlled trials run to GCP standards and prospectively registered in public clinical research domains for full transparency. This scientifically rigorous approach generates credibility with scientists and clinicians, which in turn translates to trust by consumers.”
Regulatory developments
Although generating robust clinical evidence is crucial, Naghibi notes that building consumer trust also depends on regulatory frameworks that evolve alongside scientific progress.
“Across many markets, regulatory requirements for food supplements have become increasingly rigorous over the past decade. This plays a key role in protecting consumers. In parallel, there is also a need for regulatory frameworks to enable a pathway for clinical research — especially research meeting gold standards — to be shared more broadly.”
She says that it can be challenging for regulations to match the pace at which the research is advancing, exemplifying the microbiome as an exponentially growing body of scientific evidence.
“It’s important that leaders in the microbiome research space engage in an active dialogue with regulators so that we can learn from each other and ensure that consumers have access to the most accurate information about the latest science, allowing them to make informed decisions about their health and well-being,” Naghibi concludes.
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