Panel discussion on...

Pet Supplements

Laetitia d’Ursel      , Noah Craft, MD, PhD,
Lindsey Wendt, DVM, CVA, CVFT, CCRT

1. Head of Marketing at People Science
2. Co-CEO at People Science
3. Founder at Crystal Lotus Veterinary Care

Member of AgroFOOD Industry Hi Tech's Scientific Advisory Board

Bridging the Species Gap: The Future of Clinical Evidence in Pet Supplements

We have entered the age of the “Wellness Pet”. Owners are no longer just looking to treat ailments, they are seeking to optimize longevity, replicating their own health routines for their four-legged companions. Yet, despite this sophisticated consumer demand, the foundation of the pet supplement market remains surprisingly fragile. We are building a modern industry largely on borrowed science, extrapolating human data to animal physiology. To bridge the gap between marketing promise and clinical reality, we must stop treating pets as “small humans” and start researching them as the distinct biological entities they are.

The Scientific Gap: Beyond “Human Data”

One of the most persistent scientific gaps in pet supplement development is the over-reliance on human data. While human clinical trials provide a foundational understanding of an ingredient’s Mechanism of Action (MoA), they cannot be the endpoint for pet products.


Species-specific research is not just important; it is critical. Dogs and cats have distinct metabolic variances, microbiome compositions, and absorption rates compared to humans. An ingredient that has high bioavailability in humans may be poorly absorbed or even toxic in companion animals (as seen with xylitol or certain grape-derived compounds (1)). Relying on human data or simple palatability studies creates a "translation error", where products are marketed based on theoretical benefits rather than proven efficacy in the target species.


This creates significant formulation challenges that the industry often overlooks. While palatability is essential for compliance, if they won't eat it, it won't work, it cannot come at the expense of stability and dosing accuracy. Too often, responsible formulation is hindered by a lack of clinical data on how active ingredients degrade or absorb in pet-specific formats. Without this foundational data across diverse populations of dogs and cats, formulators are forced to extrapolate, leading to products that may be tasty, but ultimately ineffective or potentially unsafe.


The industry must move toward establishing efficacy through trials conducted in the target species, at the specific dosage intended for market.

The "Humanization" Double-Edged Sword

The trend of pet humanization is a primary driver of industry growth, but it carries a risk of creating unrealistic expectations. It drives positive demand for "clean label", sustainable, and transparent ingredients, mirroring human wellness trends. Owners are increasingly scrutinizing labels for purity and sustainability, influencing purchasing decisions heavily.


We see this most clearly in the burgeoning "healthy aging" category. Driven by the human longevity movement, we are witnessing a surge in ingredients such as NAD+ precursors, senolytics, and mitochondrial support, alongside novel approaches to increase the bioavailability of classic ingredients like CoQ10. While the intent is noble, the "cognitive bias" of humanization leads consumers to assume that "human-grade" equates to "clinical efficacy" in pets.


This can lead to the widespread use of ingredients that are trendy in human wellness but lack robust data in veterinary medicine. To mitigate this risk, brands must prioritize education, explaining that a "high-quality" ingredient is only valuable if it is bioavailable and effective for that specific animal’s biology. As the longevity category expands, the clinical data supporting these sophisticated ingredients must grow accordingly.


Furthermore, we are seeing a sophistication in how owners approach these regimens. There is no longer a binary choice between simple, single-ingredient solutions and complex blends. We observe a market where owners use multi-ingredient formulations as a preventative "base," supplementing with targeted single-ingredient products for individualized care. This "stacking" approach mirrors human bio-hacking, further emphasizing the need for rigorous safety data on how these ingredients interact within the animal.

Methodological Challenges: The Case for Decentralized Trials

Perhaps the greatest hurdle in pet clinical research is the methodology itself. Historically, clinical trials for pets were conducted in laboratory settings or clinical kennels. While these controlled environments offer precision, they introduce a significant confounding variable: stress.


The "White Coat Effect" is well-documented in humans and even more pronounced in animals. A dog in a kennel environment creates different cortisol levels and behavioral responses than a dog in its home environment. This stress can skew data, particularly for supplements targeting anxiety, digestion, immune function, or mobility.


The solution lies in real-world evidence generated through decentralized clinical trials. By conducting studies in the pet’s home environment, we remove the stress variable and capture data that reflects how the product works in real life. This approach addresses the main methodological challenge of traditional trials: a lack of ecological validity. If a supplement works in a lab but not in the chaos of a real home, it fails the consumer. As with the most advanced research in humans, testing products at home with a very diverse population of pets, gives the most accurate readout of which products will really work in the real world.

The Power of Owner-Reported Outcomes

A common skepticism in veterinary research is the reliability of Owner-Reported Outcomes (ObsRO) compared to veterinary assessments. Can an owner objectively rate their dog’s mobility or scratching?


The answer is yes, but only if the study design is rigorous. In human medicine, Observer-Reported Outcomes are the gold standard for populations that cannot speak for themselves, such as infants or patients with advanced dementia. The same principles apply to veterinary research.


To ensure reliability, we must move away from retrospective surveys ("How was your dog's energy last month?") to real-time data capture ("Rate your dog's energy right now"). When integrated into a digital platform that prompts owners to log data in real-time, ObsRO becomes a highly sensitive tool. Owners see their pets for hours every day, whereas a vet sees them for 15 minutes in a stressful exam room. Integrating high-frequency ObsRO data with digital biomarkers (such as activity collar data) offers the most holistic view of a supplement's efficacy. Additionally, non-invasive sampling of feces, urine, skin swabs, or mouth swabs can be easily performed by pet companions bringing additional objective data to consider.

Navigating Claims and Trust

As the market crowds, the risk of consumer confusion rises. Claims such as "Clinically Tested" are often misunderstood. A consumer may interpret this as "proven to work," when it might simply mean the product was tested for safety, or that the ingredient was tested in a different species.


To reduce this risk, the industry needs clearer substantiation standards. "Clinically Proven" should be reserved for finished-product studies in the target species. Looking ahead 5–10 years, the brands that succeed will be those that adopt "Open Science" principles, sharing not just the marketing highlights, but the study design and full results of their clinical trials.

The Next Decade of Trust

If we could identify one single change to improve consumer trust over the next decade, it would be the democratization of clinical research. We need to make clinical trials accessible and affordable enough that they become the standard, not the exception, for every product launch. By leveraging technology to capture high-quality, real-world data from pet owners, we can close the scientific gaps and ensure that the "humanization" of pets is matched by the sophistication of the science that serves them.

Panelists

Katrin Hedvall

Head of Food Sweden AFRY

Dr. Banu Sezer

Global Market Development Manager 
Anton Paar GmbH, Graz, Austria

Dr. Adam M. Adamek , PhD

CEO, Editor-in-Chief, Food Edge, Belgium

Elizabeth Koumpan

Distinguished Engineer and CTO 
for IBM iOps organization

Kirt Phipps

Principal Scientific Consultant –

Toxicology & Regulatory Affairs, Intertek

Dayna Lozon

Scientific Consultant 1 – Toxicology and Regulatory Affairs, Intertek

Karen E. Todd, RD

VP, Global Brand Marketing
Kyowa Hakko USA

René Floris

Chief Innovation Officer, CIO, 
NIZO Food Research

Veronika Pipan

Head of Scientific Support at PharmaLinea

Dr. Mariette Abrahams MBA

CEO & Founder of Qina