One of the recurrent themes in alternative medicine is the practice of simplifying complex medical conditions, and then offering up equally simple solutions which are positioned as still being within the realm of science. This approach allows the practitioner to ignore all of the complexity and difficulty of practicing real medicine, yet offer nostrums that, on first glance, can sound legitimate. Science-y, even.

I’ve discussed this before in non-science-based approaches to food intolerances, whether it’s using clinically useless IgG blood tests, or declaring the universal dietary enemy to be gluten. David Gorski elaborated on the same theme just a few days ago in the context of cancer treatment, contrasting the simplistic views of alternative medicine purveyors with the facts of cancer research. Cancer is stunningly complex – each of the hundreds of different variants of the disease. I’m always amazed when I speak with oncologists about how treatment regimens have been established. They describe how the results of dozens of clinical trials, led by different trial groups around the world have each contributed to establishing the current “best” regimens for each cancer: the appropriate drugs, doses, intervals and treatment intensities. Good evidence speaks all languages, and as new data emerges, practices change quickly to build upon whatever new evidence has emerged. The complexity of treatments continue to increase. Overlay the genetic and genomic complexity David described, and you get a sense of the challenges (and opportunities) cancer researchers face in order for science continue to improve outcomes for patients with cancer.

So it’s a bit of a shock when you shift your attention to the alternative medicine “literature”, where simple solutions abound. One that’s popular among patients I speak with, particularly those with European backgrounds, is the use of what are called systemic enzymes – enzymes, consumed orally, with the intent of whole-body effects. These products are not used as part of “conventional” medicine but are popular supplements recommended by alternative practitioners. I was recently asked about a product called Wobenzym N, a product with German roots which is advertised with the following claims [PDF]:

Taking Wobenzym®N as directed will assist several of your body’s key systems. This product supports the musculoskeletal system by promoting health and mobility in joints and muscles, and has been used for many decades. Wobenzym®N supports the circulatory system by promoting vein health. This product also supports the respiratory system and sinus health. Wobenzym®N is used by many people in the support of a balanced immune system and assists in promoting healthy aging. Wobenzym® is safe and effective and has been used by over 100 million people for over 40 years all around the world.

Vague and non-specific claims, and there’s the Quack Miranda warning there, too. But what does Wobenzym N actually do? Other sites promoting its use go much further in their treatment statements, describing use for conditions ranging from Alzheimer’s and angina to multiple sclerosis, prostatitis, respiratory infections and right through the alphabet to uveitis. Some mention utility in treating cancer. What ties all of these disparate conditions together? There is, as David Gorski terms it, One True Cause. When you’re using systemic enzymes, your “OTC” of all illness is inflammation.

Rubor, calor, dolor, tumor

Inflammation is our body’s response to infection and injury and is part of the healing process. Diseases with an inflammatory component are common, and have a huge health impact – think of asthma, arthritis, and inflammatory bowel disease, all common, chronic illnesses affecting millions. Low grade inflammation associated with obesity may be the trigger of a number of obesity-related complications. But “inflammation” doesn’t come in one form. There are multiple mediators, such as cytokines and ecosanoids. There’s a wide variety of cellular responses. As Peter Lipson has explained before:

 Inflammation is a medical term that refers to a host of complex physiologic processes mediated by the immune system. Inflammation gets its ancient name from the obvious physical signs of inflammation: rubor, calor, dolor, tumor, or redness, heat, pain, and swelling. As the vitalistic ancient medical beliefs bowed to modern science, inflammation was recognized to be far more complex than just these four external characteristics. In addition to being a response to injury and disease, the cellular and chemical responses of inflammation can cause disease. For example, in asthma and food allergies, a type of immune reaction called type I hypersensitivity elicits a harmful type of inflammation. Coronary heart disease, the biggest killer of Americans, is believed to have a significant inflammatory component.

While there can be inflammatory components to many different diseases, it is a gross oversimplification to think that we can treat all forms in the same way, until there’s evidence to show that’s the case. Asthma and arthritis both have inflammatory elements, but they are different diseases with different treatments. But simplify the conditions to just be “inflammation” and you can introduce an equally simple solution. That solution? Systemic enzyme therapy:

Wobenzym®N works by providing “systemic enzyme support,” which describes a process that uses enzymes to assist the body’s various regulatory and communication systems, specifically the immune system.† A balanced immune system is necessary for maintaining overall health. Active enzyme molecules must be readily available in the small intestine to make sure that the systemic effect of the enzymes is achieved.

Enzymes play a critical role in the body and are involved in an astounding number of metabolic processes. Scientists suspect there may be as many as 15,000 enzymes at work in our bodies on a daily basis. Enzymes are involved in a variety of bodily processes including: breathing, growing, digesting, producing energy, conducting nerve impulses, clotting blood, recovering after exercise, or balancing the complex processes of the immune system.

Enzyme supplementation can be science-based. Its use in pancreatic disease is common, as well as diseases like cystic fibrosis. But those are not uses where the enzymes need to be absorbed from the gastrointestinal tract. Systemic enzyme replacement is something different.

I first encountered the idea of massive enzyme superdoses when I learned about the Gonzalez regimen, an alternative cancer treatment regimen discussed at length in prior posts by Kimball Atwood. The treatment includes coffee enemas and hundreds of tablets of pancreatic digestive enzymes daily. The regimen itself was based around the speculation of cancer causes which have now been definitively disproved. A clinical trial of the Gonzalez regimen was funded by the National Centre for Complementary and Alternative Medicine (NCCAM), which included a large number of pancreatic enzymes. The results of the trial were remarkable, but not in a positive way for the “alternative” approach: Conventional chemotherapy treatment for pancreatic cancer was three times better than the Gonzalez regimen.

Our pancreas secretes enzymes to help in digesting food. Should we expect that consumed enzymes will be absorbed into the body? Enzymes are large proteins that act as catalysts for biochemical reactions throughout the body – many chemical transformations are catalyzed by an enzyme. Many parameters can affect enzyme activity, including pH and temperature, and the presence of activators and inhibitors. Given the importance of enzymes in the body, genetic disorders that affect enzyme production and function can have catastrophic consequences. We’d also expect that the production and distribution of enzymes in the body would be fairly tightly controlled, given the potential effects, and given the food we eat will have its own share of naturally-occurring enzymes in it, too.

The use of proteins as therapeutic agents to influence disease is one of significant research interest. The challenge in introducing proteins into the body is that most are quickly eliminated from circulation, whether it’s by biotransformation by enzymes or renal filtration. Very large doses may be required, increasing the potential for non-specific toxicity and even allergic reactions. The most common therapeutic uses of proteins is by injection, because large chemical molecules are generally either destroyed by our endogenous digestive enzymes or, if they survive, cannot cross membranes into the bloodstream.

So the concept of giving enzymes orally, and achieve meaningful therapeutic effects in the body, is one with a considerable number of drug design hurdles. Is that occuring? Looking at Wobenzym N, each enteric coated tablet contains:

  • Bromelain 45mg
  • Chymotrypsin 1 mg
  • Pancreatin 100 mg
  • Papain 60 mg
  • Rutin 50mg
  • Trypsin 24mg

The recommended dosage is 3 tablets, twice daily, 45 minutes before meals. Before digging into the clinical data, I wanted to better understand the formulation and the dosing, keeping the design and administration issues in mind.


Every summary of a drug’s characteristics (the “monograph”) will have the same section. It’s abbreviated ADME which stands for Absorption, Distribution, Metabolism and Elimination. This is the section where behaviour of the the chemical in the body is summarized. This isn’t the clinical section, describing the therapeutic effects. It’s simply characterizing how extensively and how quickly the drug is absorbed from the gastrointestinal tract, where it distributes in the body (the “volume of distribution”) how and if it is broken down or “biotransformed” to make it easier to eliminate, and how quickly it is eliminated from the body. (I described this process in more detail in a previous post on generic drugs.) I want to see this graph, or be presented with enough data to understand what it looks like.

Plasma level curve for a drug

It’s the basic pharmacology work that’s done on a drug that gives us the information to understand its characteristics in the body. There is no point in doing clinical trials of a chemical packaged as a tablet, if we cannot confirm that the active ingredient is actually absorbed when it’s consumed. Clinical trials follow the basic pharmacology work. If the drug is treating different conditions, we may need to study different doses to establish the MEC for each condition. (For example, you need to take a lot more of an anti-inflammatory drug to treat rheumatoid arthritis than you need to treat a headache).

This is the study of pharmacokinetics, and it allows us to determine how the drug should be dosed and delivered in the body. Is it slowly eliminated, so the dosing can be infrequent – daily or even weekly? Is it rapidly eliminated from the body, meaning we need to dose multiple times a day to stay in the sweet spot of the therapeutic range? How is it eliminated from the body? Is it transformed by the liver? What impact does changing the dose have on the elimination of the product? What dose ranging studies have been done on the product that have established the appropriate dose? And how does that dose change, depending on the condition being treated?

My reason for belaboring this points is that understanding the ADME is essential to using drugs, supplements, or chemicals of any kind in a rational way. With herbs, it’s the difference between herbalism and pharmacognosy. Without it, dosing of any product is empirical – a shot in the dark. Coming back to Wobenzym N, we have a combination product with six different ingredients. The dosing instructions are very specific: 3 enteric coated tablets, twice daily, 45 minutes before meals. It’s the same for all of the different reasons for use described. But why this dose? Why 3 tablets? Why twice daily? What happens if you take more, or less? Different ingredients typically have their own physicochemical characteristics. What effects does each have? I looked at each ingredient first in the Natural Medicines Comprehensive Database (NMCD), and then in the primary literature itself. Here’s what I could find:

  • Bromelain is a term used for a collection of enzymes isolated from pineapple. While it’s rated by NMCD as “possibly effective” for osteoarthritis, the data are contradictory with some studies suggesting it has no effect on osteoarthritis. It has not been well demonstrated that bromelain reaches any clincially meaningful concentration in the blood. These are large protein molecules and it’s not clear how effectively they are absorbed – doses of 3000mg/day seem to result in tiny, albeit measurable, blood levels. Blood plasma components may inactivate any bromelain that is absorbed, though a half-life has been described [PDF]. On balance, the data are not impressive.
  • Chymotrypsin is a protein-digesting enzyme that is synthesized and secreted by the pancreas. I could locate no published efficacy of supplemental single ingredient chymotrypsin for any condition. It’s not clear what a supplemental dose of a few milligrams would have. I couldn’t locate any information that characterizes its ADME.
    Pancreatin is a mix of digestive enzymes including lipase, protease, and amylase, is used as prescription drug to treat pancreatic insufficiency, in conditions like cystic fibrosis. High doses have been linked to increases in blood/urine uric acid levels. There is no well-established use of oral pancreatin for anything other than pancreatic inefficiency. Again, little information exists to describe the ADME.
    Papain is a papaya-derived combination of enzymes. I could find a single study (in German) which compared oral supplements favourably to acyclovir for herpes zoster pain. Given the limited info in the abstract, it’s not possible to evaluate the data more fully. Little data exists to characterize the ADME.
    Rutin is a flavenoid rated as “possibly effective” for osteoarthritis on the basis of a single double-blind trial of an enzyme product (bromelain, trypsin, and rutin) versus diclofenac. Rutin does not seem to be absorbed intact, through it appears to elevate plasma levels of quercetin, and seems to have an effect on the absorption of other drugs. Again, little information exists to understand the pharmacokinetics.
  • Trypsin is another enzyme produced in the pancrease for digestion of proteins. Beyond the trial with rutin, I could locate no published trials evaluating efficacy for any other condition. Limited information exists to describe the ADME.

As I noted, getting large proteins like enzymes to be absorbed is a drug design challenge. Even if absorbed, how large molecules would escape rapid metabolism and elimination isn’t clear, either. With the ingredients in Wobenzym N, there appears to be some data to suggest that some components do reach the bloodstream. And there are some studies with the individual ingredients – but nothing that unequivocally establishes a meaningful effect. With that in mind, I looked for studies using the Wobenzym combination of ingredients.

The studies

I stared a review with the Natural Medicines Comprehensive Database (NMCD). Regarding Wobenzym N, it says, in part:

Wobenzym N is promoted for reducing inflammation and edema, and speeding recovery from certain injuries. Often it is used by individuals with arthritis and by athletes, including some professional and Olympic athletes. Enzymes in this product are thought to activate macrophages that attack inflammation-causing circulating immune complexes. Rutoside, an additional ingredient, acts as an antioxidant. To date there is no convincing clinical evidence that Wobenzym is effective for these uses. Because these enzymes do not affect prostaglandin synthesis, Wobenzym N is also promoted to be free of many of the side effects associated with non-steroidal anti-inflammatory drugs (NSAIDS). Adverse reactions reported after oral administration include loose stools, increased gas, and skin reactions.

NMCD cautions that there is also potential for the product to affect blood coagulation.

Are there clinical trials with Wobenzym? Yes, but few are in English, which complicates the review. I could locate no evaluable trials in PubMed, but other websites list trials in conditions such as pelvic inflammatory disease, cancer, and multiple sclerosis (URL Removed – Malware site! -webmaster). Some therapeutic improvements have been attributed to the consumption of Wobenzym (e.g., diabetespost-heart attack) but the studies are preliminary, sometimes unblinded, and don’t appear to be duplicated. One of the few English papers appeared in Medical Hypothesesnot a good sign for someone seeking science-based medicine. There’s an uncontrolled trial in bronchitis in children, in a study published in Russian. Other studies are published in Czech, Ukranian, Latvian, and Russian. One German systematic review declared “oral proteolytic enzyme treatment does not offer a justified alternative in comparison with NSAID in the anti-inflammatory treatment of rheumatic disease.” Overall, no large clinical trials with relevant clinical outcomes, and no persuasive evidence to demonstrate clinically meaningful effects for any single condition it is used to treat. On balance, the safety profile of the product seems acceptable, but it’s not clear how extensively safety data was captured in these small trials.

There are several trials with a similar product, Phlogenzym (rutoside, bromelain and trypsin). One didn’t suggest impressive results for ankle strains. A trial studying the same combination for hip osteoarthritis suggests non-inferiority with diclofenac, and an open-label trial for osteoarthritis of the knee found non-inferiority as well. I even found a small trial declaring it effective for treating pediatric sepsis, which left me curious if there are research ethics boards in India.

There is also the interesting case of the enzyme serrapeptase, also sold as an anti-inflammatory. Sold by the pharmaceutical company Takeda since 1968 for asthma, bronchitis, and touted as an enzyme anti-inflammatory for a large number of other uses, it was withdrawn from the Japanese market in 2011, after double-blind trials concluded that it had no therapeutic effects.

On balance, looking at the data for systematic enzymes, I wasn’t impressed. Despite the generalized claims of effectiveness, there are so many limitations in the data itself it’s not clear we can infer that the treatment effects are real. And given the lack of data on the absorption, distribution, metabolism and elimination of Wobenzym, it’s not clear that this product is even absorbed to a meaningful extent and available in the body to have systemic effects. Without any objective measure to evaluate efficacy, it’s not clear that supplementation will have any meaningful therapeutic effects for any condition, chronic or otherwise. You may feel better when you take it, but there’s no persuasive evidence yet that it’s having a meaningful effect.

This rock keeps tigers away

It would be an amazing discovery – Nobel worthy – if there were an oral therapy with demonstrably beneficial effects on a variety of chronic diseases without evidence of toxicity. Even demonstrating that large protein molecules can be consumed orally and be delivered in significant amounts to the bloodstream would be notable. Unfortunately, neither have been convincingly demonstrated with Wobenzym or other “systemic” enzyme treatments. Science is complicated, and simple solutions may be attractive, but they’re also quite possibly wrong. Given the weak clinical and pharmacokinetic data for this product, I expect that, should more research be done, it will follow the same evidence trajectory of many other supplements with an implausible premise: As the research studies improve in size and methodologic rigor, the treatment effects will disappear. Until better evidence appears to demonstrate the efficacy and safety of systemic enzyme therapy, their use can’t be considered science-based.

Posted by Scott Gavura

Scott Gavura, BScPhm, MBA, RPh is committed to improving the way medications are used, and examining the profession of pharmacy through the lens of science-based medicine. He has a professional interest is improving the cost-effective use of drugs at the population level. Scott holds a Bachelor of Science in Pharmacy degree, and a Master of Business Administration degree from the University of Toronto, and has completed a Accredited Canadian Hospital Pharmacy Residency Program. His professional background includes pharmacy work in both community and hospital settings. He is a registered pharmacist in Ontario, Canada. Scott has no conflicts of interest to disclose. Disclaimer: All views expressed by Scott are his personal views alone, and do not represent the opinions of any current or former employers, or any organizations that he may be affiliated with. All information is provided for discussion purposes only, and should not be used as a replacement for consultation with a licensed and accredited health professional.