Exciting News From Symbio | Proinnovera


Symbio & Dow Group merges with Proinnovera to form leading dermatology CRO, Symbio Proinnovera

New York, USA & Münster, Germany – November 16, 2023

The newly announced merger of NY-headquartered Symbio LLC and CA-headquartered Dow Development Laboratories LLC with Munster (Germany)-based Proinnovera will form Symbio Proinnovera, creating one of the world’s largest specialized dermatology-focused clinical
research organizations.

Founded over 20 years ago, the Symbio & Dow Group has a full-service clinical trial CRO offering for dermatology, complemented by a business active in the pre-clinical formulation of topicals, providing its client’s dermatology and aesthetics services – from pre-clinical formulation work to subsequent clinical trial execution.

Proinnovera was founded 25 years ago and is a leading European CRO in the dermatology clinical trial space. It is a full-service CRO conducting clinical studies from Phase I to IV, as well as non-interventional and medical device studies. Proinnovera turns study data into oversight for clients to accelerate decision-making, increasing transparency and efficiency in the conduct of clinical trials.

Both companies are proven market leaders among specialty dermatology CROs with exceptional geographical coverage. Their combined strength will enable them to excel at addressing customers’ needs and expectations in all areas of research.

The newly formed organization will leverage the combined power of two highly experienced teams with deep expertise in the dermatology space to generate efficiencies and accelerate clinical research.

Symbio President Rich Panico – who will become CEO of Symbio Proinnovera – commented, “I am more than excited to run what will be the leading dermatology CRO in our industry. I have always thought of Symbio and Proinnovera as not only mirror businesses on different continents but also as companies sharing common values. In fact, we wanted this partnership to happen 5 years ago. It took longer than expected but I am so thrilled it has finally happened.”

Proinnovera Founder and CEO Dr Burkhard Breuer added, “We are delighted to merge with the Symbio Group. Our entities are highly complementary in terms of services, customers, and geographical footprint; we are fully aligned and share the same ultimate objective to elevate clinical trials to the next level.” Dr Breuer will support the integration of the new organization.

Symbio Proinnovera will be supported in its growth by ARCHIMED, a leading investment firm focused exclusively on healthcare industries.

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Symbio Releases White Paper: “Atopic Dermatitis – Considerations for Clinical Trials”

The newest white paper in Symbio’s white paper series was recently released entitled, “Atopic Dermatitis: Considerations for Clinical Trials.” This paper explores the clinical research challenges involved in AD trials including lack of standardized rating scales, the need to enroll children and young people, and the impact of time of year and geographic region.

Atopic dermatitis (AD), often called eczema, is a common and often debilitating skin condition whose root cause remains unknown but is likely to be related to allergies and immune dysregulation. No curative treatment exists for this condition and management usually consists of topical corticosteroids. In more severe cases, topical calcineurin inhibitors, biologics or immunosuppressants may be necessary. Unless remission occurs, AD is a chronic disease and needs to be suppressed through medication and vigorous hygiene practices.

AD’s prevalence, lack of cure, and impact on life quality have driven continuous research and investment into novel therapies. Unless an extremely tolerable and efficacious treatment becomes available, this trend is likely to continue.


Symbio Releases White Paper: “The Clinical State of Psoriasis”

Symbio has released their latest white paper “The Clinical State of Psoriasis” which aims to explain why biologics have become so popular and why their introduction has been so disruptive to classic topical drug studies.

Psoriasis is a common and often debilitating skin disease that affects millions of Americans each year. In the last few decades a variety of different pharmaceutical interventions have been brought to market with the intention of alleviating the suffering this ailment inflicts. These efforts have coalesced into two main classes of drugs: Topical medications and systemic treatments. These systemic, biologic treatments generally come from a newer class of drugs known as monoclonal antibodies, or MABs.

As the psoriasis market expands to include new systemic agents, clinical trials and their enrollment become increasingly complex. Due to the rise of treatment options such as biologics, topical psoriasis drugs have seen slow enrollment over the last decade


Planning a Clinical Trial in Europe: Which Country to Choose?

Europe may seem small considering only about 10% of the world’s population lives there, but it’s the second largest region by the number of studies conducted according to clinicaltrials.gov.

The reasons why sponsors decide to execute their studies in Europe are multifold. Some typical reasons are listed here:

  • Access to a specific patient population
  • Incidence/prevalence of the indication compared to other regions
  • Recruitment speed
  • A global commercialization plan for the product
  • Regulatory reasons
  • Lower costs of research compared to other regions
  • Statistical reasons

There are 44 different countries in Europe, and each has unique advantages when it comes to running dermatology clinical trials. Depending on the trial complexity and specifics, a mixture of countries may be beneficial as well.

Irrespective of the particular reason for planning a study in Europe, it’s always a good idea to explore this region and take advantage of it.

There are many factors that should be considered when making the decision to run a project in Europe. Here are the most important ones:

1. Recruitment Speed
Speed is always crucial and may be the main reason to consider the European region.

The first aspect to look at is the population that a country has, as well as the number of suitable, experienced sites that can be activated.

In order to further determine the recruitment potential, also consider the availability and cost of standard care for patients and health care providers, the incidence/prevalence of the indication, as well as any climate-related disease aspects. The cultural attitude toward a disease can play quite an important role, too. Also, the socio-economic environment may play into whether a country has a large or a limited recruitment potential, as depending on the wealth of a country and its inhabitants, the perceived need for a certain treatment may be higher or lower.

Recruitment potential in indications such as atopic dermatitis or psoriasis is typically favorable in Eastern Europe.While topical corticosteroids are readily available, the related out-of-pocket costs for patients can be perceived as a burden and may lead to interest in study participation.

The speed of recruitment is not only relevant for the duration of a clinical study, but is also a major driver for total study costs. In particular in the area of dermatology, where studies are typically rather short, it may not only be faster, but it may even be more cost effective to activate a higher number of sites to lower the overall study costs by a shortening the duration.

2. Study Cost
When it comes to the cost of a study, the expenses of labor and site fees are typical highest in countries in Western and Northern Europe, such as the UK (still), Ireland, Sweden, Denmark and the Netherlands.

Southern European costs for labor tend to be a bit lower, and the further east a study is conducted, the lower the costs of labor will typically be. Study costs in Eastern Europe can be up to 40% lower compared with Western European or US costs.

3. Regulatory Environment
The current European Union clinical directive EU 2001/20/EC regulates the fundamental requirements for conducting clinical trials in Europe, however requirements may be stricter within an individual country, and beneath the regulatory aspects there are other important drivers when choosing a good study country.

The regulatory pathway for starting a study is important to consider, in particular when the date of First Patient In is a relevant corporate milestone for a sponsor. In some European countries (e.g., Belgium) there are regulatory pathways that allow for a shorter study start, compared with the timelines that are set in the European directive.

Next to study costs, start-up timelines and recruitment speed, some sponsors are interested in detailed exchange with regulatory bodies already in the early clinical development phase to ensure that a subsequent marketing authorization application addresses all relevant clinical development factors and leads to swift approval. In this case it is good to choose a country whose regulatory authority is well recognized among the other EU authorities and with EMA.

4. Investigator Motivation
Finally, an absolutely critical factor for study success is the motivation of a site and Principal Investigator (PI) to participate in and actively contribute to a clinical trial. There are countries in Europe where sites and PIs are more eager to participate in a study compared to other countries, and it is wise to choose a region where PIs and sites are generally very motivated to take part in research.

Financial remuneration plays an important role as well. While the site fees should always be within reasonable boundaries, it is still true that clinical research is an industry and the level of site fees influences the site´s motivation for participation. Further, the novelty of the compound, its likelihood for being effective and safe, (i.e., the likelihood that it is able to make a real change for patients) is typically an important motivating factor.

Final Thoughts
In summary, each study is unique and requires a special attitude and custom project plan, which corresponds with development goals and sponsor needs.

Located in the very center of Europe, Symbio’s office in Germany has all the capabilities necessary to support any clinical development program in the European region. Our team members have significant experience in clinical research and have conducted clinical trials in the vast majority of European countries from Scandinavia to Southern Europe, and from Ireland to Russia in the last twenty years.

Depending on the drug type, phase and specifics of the project, Symbio’s experts will suggest the best geographical location for the study and support the project locally.

Reach out to me directly to discuss your project and how Symbio Europe can be a valuable partner.

Veronika Kunert, Chief Operating Officer, Symbio Europe