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
References and notes
- Kovalkovičová, N., Šutiaková, I., Pistl, J., & Šutiak, V. (2009). Some food toxic for pets. Interdisciplinary Toxicology, 2(3), 169–176. https://doi.org/10.2478/v10102-009-0012-4
Questions
1.
2.
3.
4.
Ingredients companies - clinical data
A) What are the main scientific gaps that still exist in PET supplement development compared to human dietary supplements?
B) How important is species-specific research when selecting and developing active ingredients for pets? Can human data ever be sufficient?
C) Is the humanization of pets helping consumers make better-informed choices, or does it risk creating unrealistic expectations about supplement performance?
D) From an ingredient supplier’s perspective, which quality parameters (standardization, bioavailability, purity) are most critical for PET applications?
E) How are trends such as “clean label,” sustainability, and transparency influencing pet owners’ purchasing decisions in the PET supplement space?
F) What type of clinical evidence should realistically be expected to support PET supplement claims today?
G) Which types of claims are most likely to be misunderstood by consumers, and how can this risk be reduced through clearer substantiation and labeling?
H) What are the main methodological challenges in conducting clinical trials for companion animals, and how can they be addressed?
I) How reliable are owner-reported outcomes compared to veterinary assessments, and how should they be integrated into study design?
L) Have you noticed an increasing trend in the use of one (or more) ingredients for pet supplements formulated to promote healthy ageing?
Formulation
A) What are the biggest formulation challenges in PET supplements, particularly regarding palatability, stability, and dosing accuracy?
B) How do formulation choices (e.g., chews, powders, liquids) influence compliance and consistent use from a consumer perspective?
C) Do you see a shift toward simpler, single-ingredient formulations, or are multi-active blends still the dominant approach? Why?
D) How do species differences (dogs vs cats, size, age) influence formulation strategies?
E) Omega 3 alternatives for pet nutrition and sustainability: how do the innovative omega-3s for pet food stack up against their traditional fishy counterparts?
Regulation
A) How do regulatory frameworks for PET supplements differ between the EU and the US, and what challenges do these differences create for global brands?
B) Which types of claims represent the highest regulatory risk today, and which are more likely to be acceptable if properly substantiated?
C) Do you expect regulatory oversight of PET supplements to become stricter in the coming years? Why or why not?
D) What role should veterinarians play in guiding pet owners’ choices regarding PET supplements, and how can trust between brands, vets, and consumers be strengthened?
Open questions
A) Looking ahead 5–10 years, what will be the key factors determining the credibility and long-term success of the PET supplements sector?
B) In your view, what single change—scientific, regulatory, or educational—would most improve consumer trust in PET supplements over the next decade?
References and notes










