About Us
About Us

Formulation science that enables tomorrow’s biologics

Formulation science that enables tomorrow’s biologics

20 years of experience. Data-driven strategies. Trusted by biotech, mid-size pharma, and global leaders.


20 years of experience. Data-driven strategies. Trusted by biotech, mid-size pharma, and global leaders.

Laboratory staff
Who we are
Who we are

Relentless about stability & speed

Relentless about stability & speed

We design tailored formulations for sterile injectables, e.g. antibodies, bispecifics, viral vectors, and vaccines by combining molecular modeling, bioinformatics, and biostatistics with hands-on lab expertise. We are aware that every molecule is different. That’s why our cross-functional labs develop data-driven formulations tuned to your specific biologic and CMC timeline.

We design tailored formulations for sterile injectables, e.g. antibodies, bispecifics, viral vectors, and vaccines by combining molecular modeling, bioinformatics, and biostatistics with hands-on lab expertise. We are aware that every molecule is different. That’s why our cross-functional labs develop data-driven formulations tuned to your specific biologic and CMC timeline.

Laboratory staff

We’re bringing a data-driven mindset to formulation science by combining deep biologics expertise with advanced data science. This allows for de-risking and accelerating the development of robust, scalable drug products.

Laboratory staff
Michael Scholl

CEO

Our history
Our history

Our history is our heritage

Leukocare was founded in 2003 by Prof. Martin Scholz and Michael Scholl, with an initial focus on stabilizing biomolecules for functionalization of medical devices. This pioneering work in protein stabilization laid the foundation for our expertise in drug product formulation.


We have evolved into a trusted partner for biotech, mid-size pharmaceutical companies, and leading global players, who turn to us for our deep modality experience and our rigorous data-driven formulation strategies. Our portfolio spans monoclonal and bispecific antibodies, viral vectors for gene therapy, vaccines, and other complex biologics.




Laboratory assistant
Laboratory assistant
Laboratory assistant
Laboratory assistant
Laboratory assistant
Laboratory assistant

To strengthen our scientific foundation, we established dedicated teams in bioinformatics and biostatistics, enabling us to integrate molecular modeling, predictive analytics, and statistical design of experiments into every stage of formulation development.

Today, stability remains in our DNA as we continue our journey as a fully integrated service provider for complex drug product development — combining scientific rigor with proven industry trust.

Leadership Team

Executive Team: Steering vision, strategy and day-to-day execution.

Executive Team: Steering vision, strategy and day-to-day execution.

Michael Scholl
Chief Executive Officer (CEO)
Michael Scholl

Michael is CEO and Co-Founder of Leukocare, heading strategy, finance, corporate law, marketing & sales and HR. Before joining Leukocare, Michael was an entrepreneur and investor and founded several technology companies. He started his career as business consultant at BCG. Michael holds a master’s degree in business engineering from the University of Berlin.

Dr. Cornelius Pompe
Chief Operating Officer (COO)
Dr. Cornelius Pompe

Cornelius brings more than 15 years of experience in early and late stage biopharmaceutical development. Before joining Leukocare, Cornelius served as Drug Product Development Head, Early Operations Lead and Member of the Process Development Senior Leadership Team at Amgen Research Munich/Micromet. Prior to his roles at Amgen/Micromet, he held several roles in the area of drug product development such as Head of Freeze-Dried Drug Product Development Unit at LFB (France) and Head of Formulation Development and Project Coordination at Coriolis. Cornelius holds a PhD in Pharmaceutical Technology from Ludwig Maximilians University Munich.

Leadership Team

Executive Team: Steering vision, strategy and day-to-day execution.

Executive Team: Steering vision, strategy and day-to-day execution.

Michael Scholl
Chief Executive Officer (CEO)
Michael Scholl

Michael is CEO and Co-Founder of Leukocare, heading strategy, finance, corporate law, marketing & sales and HR. Before joining Leukocare, Michael was an entrepreneur and investor and founded several technology companies. He started his career as business consultant at BCG. Michael holds a master’s degree in business engineering from the University of Berlin.

Dr. Cornelius Pompe
Chief Operating Officer (COO)
Dr. Cornelius Pompe

Cornelius brings more than 15 years of experience in early and late stage biopharmaceutical development. Before joining Leukocare, Cornelius served as Drug Product Development Head, Early Operations Lead and Member of the Process Development Senior Leadership Team at Amgen Research Munich/Micromet. Prior to his roles at Amgen/Micromet, he held several roles in the area of drug product development such as Head of Freeze-Dried Drug Product Development Unit at LFB (France) and Head of Formulation Development and Project Coordination at Coriolis. Cornelius holds a PhD in Pharmaceutical Technology from Ludwig Maximilians University Munich.

Supervisory Board: Independent governance and strategic guidance.

Independent industry veterans and investment leaders providing governance, capital-market insight, and long-term strategic direction.

Tadd Wessel
Chair
Tadd Wessel

Tadd Wessel is the Founder and Managing Partner of Petrichor, a private equity firm focused on the healthcare sector. Tadd was formerly a Managing Director at OrbiMed Advisors and Vice President at Fortress Investment Group. Tadd sits on numerous boards of directors of life sciences companies. He holds an A.B. in Biology from Princeton University.

Dr. Andreas Rummelt
Board Member
Dr. Andreas Rummelt

Dr. Andreas Rummelt is Partner and CEO of InterPharmaLink AG, a Management Consulting firm in Basel, Switzerland. His international career in pharmaceuticals has focused on the areas of manufacturing, quality, technical development and generics and he has served more than twenty years in executive management positions in the industry. From 2004 to 2008, Dr. Rummelt was CEO of Sandoz in Vienna and Holzkirchen. He also served as Group Head of Quality Assurance and Technical Operations at Novartis, a position he held from 2008 until 2010, and he had been a member of the Executive Committee of Novartis from 2006 until his resignation in 2010. Dr. Rummelt is a pharmacist and holds a Ph.D. degree from the University of Erlangen-Nuremberg.

Dr. Jean-Paul Prieels
Board Member
Dr. Jean-Paul Prieels

Jaul-Paul Prieels holds a PhD in Biochemistry from Université Libre de Bruxelles in Belgium. After ten years at university, he started his industrial career at Petrofina in 1983 as Biotechnology Manager and joined GlaxoSmithKline Biologicals in 1987. His responsibilities gradually expanded to lead the vaccine preclinical R&D development activities in Rixensart, Belgium, and he retired as Senior Vice President of Research & Development in 2011. He was instrumental in the development of several commercially available vaccines, such as Rotarix, Cervarix and Synflorix. Today, he is Director at various companies and member of the Scientific Advisory Board of Singapore Bioprocessing Technology Institute and MolMed SPA. He is also a member of the European Vaccine Initiative Board of Stakeholders.

Dr. Maximilian Rittmeister
Board Member
Dr. Maximilian Rittmeister

Dr. Maximilian Rittmeister is a corporate lawyer and managing shareholder of a German corporate law firm. He holds a Ph.D. degree in M&A law from Johann Wolfgang von Goethe – University in Frankfurt/Main, Germany. Dr. Rittmeister is a member of several supervisory and advisory boards and also acts as a private equity investor. He is married, has two sons, and lives near Frankfurt/Main, Germany.

Board Member
Dr. Gerhard Ries

Dr. Wolfgang Schwandner is a business angel and investor in several health care and life science companies. He is founder of various pharmaceutical and health care companies focusing on generic manufacturing, wholesaling and service, and has more than 20 years of experience in executive positions in the international pharmaceutical industry. He holds a diploma and a PhD degree in Biology from Ludwig-Maximilians-Universität and Technische Universität München. Wolfgang is married, has two daughters and lives near Munich.

Dr. Wolfgang Schwandner
Board Member
Dr. Wolfgang Schwandner

Dr. Wolfgang Schwandner is a business angel and investor in several health care and life science companies. He is founder of various pharmaceutical and health care companies focusing on generic manufacturing, wholesaling and service, and has more than 20 years of experience in executive positions in the international pharmaceutical industry. He holds a diploma and a PhD degree in Biology from Ludwig-Maximilians-Universität and Technische Universität München. Wolfgang is married, has two daughters and lives near Munich.

Scientific Advisory Board: World-class scientists who keep our innovation edge sharp.

Globally renowned scientists who channel the latest academic breakthroughs into our formulation technologies and R&D pipeline.

Dr. Andreas Seidl
Chairman
Dr. Andreas Seidl

Dr. Andreas Seidl is Chairman of Leukocare’s Scientific Advisory Board and coordinates the activities of the members of the SAB to support Leukocare´s innovation processes in bioinformatics, analytics, and drug product development. Andreas is CSO of Formycon, leading the preclinical and clinical development, bioanalytics and Scientific Affairs functions. He has over 20 years experience in analytical and pharmaceutical development of biologics and contributed to the development and approval of many biosimilar products and NBEs. He has held different positions with growing responsibility at Hexal AG, Sandoz Biopharmaceuticals and Novartis. Andreas is a chemist by training with a master’s degree from the University of Constance/Germany and received his Ph.D. in the area of protein analysis and mass spectrometry from the University of Constance.

Prof. Johannes Buchner
Board Member
Prof. Johannes Buchner

Prof. Johannes Buchner received his PhD from the University of Regensburg, Germany. After a postdoctoral stay at the National Cancer Institute of the NIH in Bethesda, USA, he was a group leader at the University of Regensburg. Since 1998 he is a professor for Biotechnology at the Technical University of Munich/ Germany. He is a member of the Leopoldina, the German National Academy of Sciences. His research interests include mechanistic studies on molecular chaperones, principles of antibody/protein folding and association, as well as their evolution. Johannes Buchner received several prizes for his work, including the Hans Neurath Award, the Kossel-Award, the Max Bergmann Medal and the Schleiden Medal. He has authored 275 publications in peer-reviewed journals.

Prof. Paul Dalby
Board Member
Prof. Paul Dalby

Prof. Paul Dalby is Director of the EPSRC Centre for Doctoral Training in Emergent Macromolecular Therapies, Co-Director of the EPSRC Future Targeted Healthcare Manufacturing Hub, and Deputy Head of the Department of Biochemical Engineering at University College London. He also Chairs the Biotechnology Group of the Royal Society of Chemistry. His research focuses on routes to improve therapeutic proteins for ease of manufacture, formulation and delivery to patients. He combines protein engineering and formulation, with biophysical characterisation, molecular modelling and simulation, to understand the factors that influence protein stability, and to guide protein engineering and formulation for improved properties. He has authored over 90 numerous publications in peer-reviewed journals. Prof. Ulrike Protzer Prof. Ulrike Protzer More information

Prof. Ulrike Protzer
Board Member
Prof. Ulrike Protzer

Prof. Ulrike Protzer studied medicine in Germany, South Africa and Switzerland. She is an expert clinical virologist with clinical training in infectious diseases and hepatology before she focused on virology. Her scientific efforts focus on understanding the interaction between viruses and their hosts and on translating this knowledge into novel therapies and vaccines. Since 2007, she is a professor for Virology at the Technical University of Munich and at Helmholtz Zentrum Muenchen. She is leading three national and international research consortia, was member of the executive board of the German Center for Infection Research and now is the speaker of its Thematic Translational Unit “Viral Hepatitis”. She has published more than 145 peer-reviewed papers and 30 review articles and holds several international patents.

Prof. Theodore W. Randolph
Board Member
Prof. Theodore W. Randolph

Prof. Theodore W. Randolph has more than 30 years of experience in Pharmaceutical Biotechnology . He is professor and Co-Director at the Center for Pharmaceutical Biotechnology, University of Colorado/Boulder. His research interests include stabilization and formulation of Therapeutic Proteins- “Converting Molecules into Drugs”, application of biophysical methods for formulation development, aggregation & immunogenicity of protein therapeutics, and stability of protein-based vaccines. He has published more than 230 scientific articles in peer-reviewed journals, has been rewarded 14 research awards and is editorial board member of several scientific journals.

Prof. Bernhardt Trout
Board Member
Prof. Bernhardt Trout

Bernhardt L. Trout is the Raymond F. Baddour, ScD, (1949) Professor of Chemical Engineering at MIT. He received his S.B. and S.M. degrees from MIT and his Ph.D. from the University of California at Berkeley. In addition, he performed post-doctoral research at the Max-Planck Institute. Trout’s research focuses on the development of advanced manufacturing processes and rational tools for formulation and product design, primarily liquid formulations, but also lyophilized formulations. A major aspect of his work relates to the development of both microscopic and macroscopic models to design stable formulations efficiently. Together with colleagues from MIT, he set-up the Novartis-MIT Center for Continuous Manufacturing in 2007 which until 2019 actively pursued the objective of transforming pharmaceutical production. He has published over 200 papers and has 18 patents issued or pending. For more information on Prof. Trout and his research, please visit: http://web.mit.edu/troutgroup/

Our Facility and Location
Our Facility and Location

All laboratory operations are conducted at our Martinsried (Germany) facilities, spanning more than 2,000 m² in one of Europe’s leading biotech hubs. Our infrastructure is designed to meet the complex requirements of modern biologic drug product development while offering the flexibility needed for diverse modalities

All laboratory operations are conducted at our Martinsried (Germany) facilities, spanning more than 2,000 m² in one of Europe’s leading biotech hubs. Our infrastructure is designed to meet the complex requirements of modern biologic drug product development while offering the flexibility needed for diverse modalities

Laboratory staff
Laboratory staff
Comprehensive Formulation and Analytical Capabilities
Comprehensive Formulation and Analytical Capabilities

Our teams support projects across multiple classes of modalities — including monoclonal and bispecific antibodies, viral vectors, peptides, and vaccines — in liquid, lyophilized, and spray‑dried dosage forms. To ensure robust development, our in‑house analytical platform includes over 150 test methods, covering stability, excipient compatibility, and process performance assessments.

Our teams support projects across multiple classes of modalities — including monoclonal and bispecific antibodies, viral vectors, peptides, and vaccines — in liquid, lyophilized, and spray‑dried dosage forms. To ensure robust development, our in‑house analytical platform includes over 150 test methods, covering stability, excipient compatibility, and process performance assessments.

A trusted Development Environment

From high‑concentration antibody formulations to lyophilized virus products, our Martinsried facilities provide the environment, advanced technologies, and expert teams required to accelerate complex drug product development programs for parenteral use — from early feasibility to life-cycle management.

Quality and Commitment
Quality and Commitment

Quality at the Core

Quality at the Core

Our ISO 13485- and 9001-aligned Quality Management System (QMS) ensures rigor, compliance, and traceability at every stage of drug product development.

Our ISO 13485- and 9001-aligned Quality Management System (QMS) ensures rigor, compliance, and traceability at every stage of drug product development.

Laboratory staff
Robust Analytical Foundations

Scientifically sound, fit for purpose analytical methods are the foundation of successful formulation development.


  • Methods are selected based on product specific prior knowledge and the critical quality attributes to be addressed.


  • Depending on project needs, methods range from verified assays (including stability indicating properties and autosampler stability) to custom-developed methods fully qualified under ICH Q2 standards.


  • Risk assessments and mitigation strategies are continuously applied to anticipate and control potential challenges.

A Quality System Built for Reliability

Our QMS is uniquely comprehensive for a development focused company. It includes:

  • Standardized operating procedures (SOPs) for all equipment and methods

  • Rigorous training protocols to ensure consistency


  • Exclusive use of calibrated and maintained equipment


  • Comprehensive planning and reporting processes


  • Full traceability of materials, methods, and equipment


  • Annual internal audits and strict handling of deviations with corrective and preventive actions (CAPAs) .


  • Supplier qualification and auditing, along with controlled inventory and logistics processes

Data Integrity by Design

To further strengthen reliability, our automated data pipelines connect data generation, migration, evaluation, visualization, and storage.


  • This minimizes manual intervention, ensuring consistency and integrity.


  • All codes are developed in‑house and remain fully accessible, reinforcing transparency and accountability.

Let’s Build the Right Formulation — Together

Partner with Leukocare for tailored, data‑driven solutions that bring your biologics closer to patients.

Let’s Build the Right Formulation — Together

Partner with Leukocare for tailored, data‑driven solutions that bring your biologics closer to patients.

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