Project acronym ACTIVEPHANTOM
Project Active Organ Phantoms for Medical Robotics
Researcher (PI) Peer FISCHER
Host Institution (HI) MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV
Call Details Proof of Concept (PoC), PC1, ERC-2016-PoC
Summary Robot-assisted and minimally invasive medical procedures are impacting medical care by increasing accuracy, reducing cost, and minimizing patient discomfort and recovery times after interventions. Developers of commercial robotic surgical systems and medical device manufacturers look for realistic phantoms that can be used in place of animal experiments or cadavers to test procedures and to train medical personnel. Existing phantoms are either made from hard materials, or they lack anatomical detail, and they are mainly passive and thus unrealistic.
Here, we use recently developed fabrication know-how and expertise within our ERC-funded research to develop the first active artificial urinary tract model that includes a kidney, a bladder, and a prostate. Rapid prototyping is combined with a fabrication step that we have developed to permit the incorporation of active elements, such as a peristaltic system and fluidic valves in the phantom. We have developed smart material composites that reproduce the mechanical and haptic properties, and that give ultrasound contrast indistinguishable from real organs, while permitting anatomical details to be reproduced with a mean error of as little as 500 microns.
Feedback from a major medical device company indicates that ours is a unique phantom with unprecedented accuracy for which there is a market. Within this POC grant we want to develop a complete prototype, and to demonstrate a series of medical interventions on the phantom, including endoscopic diagnostic procedures (cystoscopy and ureterorenoscopy) and endoscopic treatment procedures (laser lithotripsy). The grant will allow us to protect our know-how, identify further markets, and develop a commercialization strategy.
Overall, this project will generate the first active phantom system that permits the testing of surgical instruments and procedures, with a sizeable market potential.
Summary
Robot-assisted and minimally invasive medical procedures are impacting medical care by increasing accuracy, reducing cost, and minimizing patient discomfort and recovery times after interventions. Developers of commercial robotic surgical systems and medical device manufacturers look for realistic phantoms that can be used in place of animal experiments or cadavers to test procedures and to train medical personnel. Existing phantoms are either made from hard materials, or they lack anatomical detail, and they are mainly passive and thus unrealistic.
Here, we use recently developed fabrication know-how and expertise within our ERC-funded research to develop the first active artificial urinary tract model that includes a kidney, a bladder, and a prostate. Rapid prototyping is combined with a fabrication step that we have developed to permit the incorporation of active elements, such as a peristaltic system and fluidic valves in the phantom. We have developed smart material composites that reproduce the mechanical and haptic properties, and that give ultrasound contrast indistinguishable from real organs, while permitting anatomical details to be reproduced with a mean error of as little as 500 microns.
Feedback from a major medical device company indicates that ours is a unique phantom with unprecedented accuracy for which there is a market. Within this POC grant we want to develop a complete prototype, and to demonstrate a series of medical interventions on the phantom, including endoscopic diagnostic procedures (cystoscopy and ureterorenoscopy) and endoscopic treatment procedures (laser lithotripsy). The grant will allow us to protect our know-how, identify further markets, and develop a commercialization strategy.
Overall, this project will generate the first active phantom system that permits the testing of surgical instruments and procedures, with a sizeable market potential.
Max ERC Funding
150 000 €
Duration
Start date: 2017-03-01, End date: 2018-08-31
Project acronym AutoLiqHand
Project A Compact and Automated Liquid Handling Platform for Biomedical Assays
Researcher (PI) Andreas Richard Dr. Bausch
Host Institution (HI) TECHNISCHE UNIVERSITAET MUENCHEN
Call Details Proof of Concept (PoC), PC1, ERC-2016-PoC
Summary Liquid handling is an integral part of biological and medical assays. For many applications the method of choice is manual pipetting, which has significant limitations. Chiefly, it is user-time intensive and prone to sample handling issues (poor time accuracy and pipetting errors). While liquid handling robots do exist, they are expensive instruments, shared by many users and targeted for high-throughput applications. This leaves, in practice, most research and diagnostics without an automated solution. Here, we present an innovative solution to this problem: a compact and mobile automated liquid handling (AutoLiqHand) device for the individual user. This platform will enable to automate biomedical experiments and diagnostic routines which are currently done by hand. Moreover, its unique design enables it to run in a much larger range of biomedical settings than currently offered by existing solutions, and at the fraction of the cost. This platform was developed as part of the ERC-funded project SelfOrg and is routinely used in our lab for a variety of specialized and standard routines (e.g. drug treatment and immunostaining). The AutoLiqHand system mimics the main advantages of manual pipetting, namely simplicity and versatility, through a unique design of a fully integrated and microfluidic-based platform. In addition, when interfaced with well-established biomedical equipment such as ELISA readers or PCR machines, our platform can form a fully automated lab at significantly lower costs than commercially available devices. Thus, it has the potential to become a standard tool for researchers both in basic and early pharmaceutical/clinical research as well as for clinicians in point-of-care diagnostics. The aim of this Proof-of-Concept proposal is to adapt the AutoLiqHand platform to market needs and optimize it for production in order to make it available to the market.
Summary
Liquid handling is an integral part of biological and medical assays. For many applications the method of choice is manual pipetting, which has significant limitations. Chiefly, it is user-time intensive and prone to sample handling issues (poor time accuracy and pipetting errors). While liquid handling robots do exist, they are expensive instruments, shared by many users and targeted for high-throughput applications. This leaves, in practice, most research and diagnostics without an automated solution. Here, we present an innovative solution to this problem: a compact and mobile automated liquid handling (AutoLiqHand) device for the individual user. This platform will enable to automate biomedical experiments and diagnostic routines which are currently done by hand. Moreover, its unique design enables it to run in a much larger range of biomedical settings than currently offered by existing solutions, and at the fraction of the cost. This platform was developed as part of the ERC-funded project SelfOrg and is routinely used in our lab for a variety of specialized and standard routines (e.g. drug treatment and immunostaining). The AutoLiqHand system mimics the main advantages of manual pipetting, namely simplicity and versatility, through a unique design of a fully integrated and microfluidic-based platform. In addition, when interfaced with well-established biomedical equipment such as ELISA readers or PCR machines, our platform can form a fully automated lab at significantly lower costs than commercially available devices. Thus, it has the potential to become a standard tool for researchers both in basic and early pharmaceutical/clinical research as well as for clinicians in point-of-care diagnostics. The aim of this Proof-of-Concept proposal is to adapt the AutoLiqHand platform to market needs and optimize it for production in order to make it available to the market.
Max ERC Funding
149 750 €
Duration
Start date: 2017-01-01, End date: 2018-06-30
Project acronym BOXMATE
Project Mining Sandboxes for Automatic App Protection
Researcher (PI) Andreas Zeller
Host Institution (HI) UNIVERSITAT DES SAARLANDES
Call Details Proof of Concept (PoC), PC1, ERC-2016-PoC
Summary Today’s industry is more vulnerable to cyberattacks than ever. The biggest threat comes from advanced
persistent threats that targets the sensitive data of a specific company. Such a threat may come along as
an innocuous app that starts its malicious behavior only when the mobile logs into the corporate network.
At the same time, such threats can be made undetectable through testing or code analysis.
The ERC SPECMATE project has developed a technology named BOXMATE that protects against unexpected
changes of app behavior and thus drastically reduces the attack surface of mobile applications.
The key idea is to mine app behavior by executing generated tests, systematically exploring the program’s
accesses to sensitive data. During production, the app then is placed in a sandbox, which prohibits
accesses not seen during testing.
This combination of test generation and sandboxing effectively protects against advanced persistent
threats. To access sensitive data during production, the app already must do so during testing—where
tracing makes it easy to discover and assess. BOXMATE neither does not need to collect user data: All
app behavior is assessed during testing already. Finally, BOXMATE requires no knowledge about source
or binary code, and thus easily handles arbitrarily obfuscated or obscure third-party apps. BOXMATE is
currently being patented worldwide.
We want to turn the BOXMATE approach into a full mobile security solution for corporate and end
users. This proposal aims at producing a full-fledged prototype that can be demonstrated to potential
customers, most notably app vendors and mobile infrastructure providers; as well as developing an
adequate marketing strategy exploring and responding to the needs of the market.
This proposal is fueled by the principal investigator, Andreas Zeller, one of the world’s leading experts
in software test generation and specification mining.
Summary
Today’s industry is more vulnerable to cyberattacks than ever. The biggest threat comes from advanced
persistent threats that targets the sensitive data of a specific company. Such a threat may come along as
an innocuous app that starts its malicious behavior only when the mobile logs into the corporate network.
At the same time, such threats can be made undetectable through testing or code analysis.
The ERC SPECMATE project has developed a technology named BOXMATE that protects against unexpected
changes of app behavior and thus drastically reduces the attack surface of mobile applications.
The key idea is to mine app behavior by executing generated tests, systematically exploring the program’s
accesses to sensitive data. During production, the app then is placed in a sandbox, which prohibits
accesses not seen during testing.
This combination of test generation and sandboxing effectively protects against advanced persistent
threats. To access sensitive data during production, the app already must do so during testing—where
tracing makes it easy to discover and assess. BOXMATE neither does not need to collect user data: All
app behavior is assessed during testing already. Finally, BOXMATE requires no knowledge about source
or binary code, and thus easily handles arbitrarily obfuscated or obscure third-party apps. BOXMATE is
currently being patented worldwide.
We want to turn the BOXMATE approach into a full mobile security solution for corporate and end
users. This proposal aims at producing a full-fledged prototype that can be demonstrated to potential
customers, most notably app vendors and mobile infrastructure providers; as well as developing an
adequate marketing strategy exploring and responding to the needs of the market.
This proposal is fueled by the principal investigator, Andreas Zeller, one of the world’s leading experts
in software test generation and specification mining.
Max ERC Funding
150 000 €
Duration
Start date: 2017-09-01, End date: 2019-02-28
Project acronym BrainControl
Project Stable Brain-Machine control via a learnable standalone interface
Researcher (PI) Rui Manuel Marques Fernandes da Costa
Host Institution (HI) FUNDACAO D. ANNA SOMMER CHAMPALIMAUD E DR. CARLOS MONTEZ CHAMPALIMAUD
Call Details Proof of Concept (PoC), PC1, ERC-2015-PoC
Summary Non-invasive Brain Machine Interfaces (BMI) bring great promise for neuro-rehabilitation and neuro-prosthesis, as well as for brain control of everyday devices and performance of simple tasks. Over the last 15 years the interest in BMIs has grown substantially, and a variety of interfaces have been developed. The field has been growing dramatically, and market studies reveal an estimated market size of $1.46 billion by 2020. However, non-invasive BMIs have failed to reach the impressive control seen by BMIs implanted in the brain. To date, they require considerable training to reach a moderate level of control, they are susceptible to noise and interference, do not generalize between people and devices, and performance does not show long-term consolidation. Results from our ERC-funded work uncovered a new paradigm that dramatically improves these issues. We propose to develop a prototype for a novel, standalone, non-invasive, noise-resistant BMI, based on an unexplored BMI learning paradigm. In this POC we will 1) refine the brain signal interface (decoder) to be automatically customizable to each individual and produces faster training, 2) implement our BMI technology into a portable hardware-based system, and 3) develop a virtual reality/gaming training platform that will increase learning, performance and consolidation of BMI control. In addition to these technical aims, we propose to explore commercial opportunities and societal benefits, in particular in the health sector. We will conduct market analysis and develop a business case for this product, while expanding industry contacts for production and commercialization.
The work proposed in this PoC grant will permit, for the first time to our knowledge, the development of a portable, stand-alone, noise-resistant, and easy to learn BMI, applicable across a wide set of devices, which will bring a significant social impact in health, entertainment and other applications.
Summary
Non-invasive Brain Machine Interfaces (BMI) bring great promise for neuro-rehabilitation and neuro-prosthesis, as well as for brain control of everyday devices and performance of simple tasks. Over the last 15 years the interest in BMIs has grown substantially, and a variety of interfaces have been developed. The field has been growing dramatically, and market studies reveal an estimated market size of $1.46 billion by 2020. However, non-invasive BMIs have failed to reach the impressive control seen by BMIs implanted in the brain. To date, they require considerable training to reach a moderate level of control, they are susceptible to noise and interference, do not generalize between people and devices, and performance does not show long-term consolidation. Results from our ERC-funded work uncovered a new paradigm that dramatically improves these issues. We propose to develop a prototype for a novel, standalone, non-invasive, noise-resistant BMI, based on an unexplored BMI learning paradigm. In this POC we will 1) refine the brain signal interface (decoder) to be automatically customizable to each individual and produces faster training, 2) implement our BMI technology into a portable hardware-based system, and 3) develop a virtual reality/gaming training platform that will increase learning, performance and consolidation of BMI control. In addition to these technical aims, we propose to explore commercial opportunities and societal benefits, in particular in the health sector. We will conduct market analysis and develop a business case for this product, while expanding industry contacts for production and commercialization.
The work proposed in this PoC grant will permit, for the first time to our knowledge, the development of a portable, stand-alone, noise-resistant, and easy to learn BMI, applicable across a wide set of devices, which will bring a significant social impact in health, entertainment and other applications.
Max ERC Funding
149 625 €
Duration
Start date: 2016-09-01, End date: 2018-02-28
Project acronym CellScreenChip
Project All-in-One Cell Screening Chip: Device for Affordable High-Throughput Cell Screenings
Researcher (PI) Pavel Levkin
Host Institution (HI) KARLSRUHER INSTITUT FUER TECHNOLOGIE
Call Details Proof of Concept (PoC), ERC-2015-PoC, ERC-2015-PoC
Summary Experiments with live cells are fundamentally important in biology, pharmaceutical industry, biotechnology or in medicine and diagnostics. One important example of cell experiments is the prescreening of cells from cancer biopsies with anticancer drugs in order to identify the most effective and least toxic combination of drugs for a particular patient also known as personalized medicine.
The goal of this ERC Proof-of-Concept project is to develop, fabricate and optimize a device (CellScreenChip) for performing miniaturized, parallel and, therefore, more affordable and faster cell screening experiments for the areas of diagnostics and personalized medicine. Applications of the CellScreenChip include (but not limited to) cell based disease diagnosis (e.g. cancer diagnostics), drug screening (e.g. body on a chip) or personalized medicine (e.g. personalized drug compatibility tests). The CellScreenChip will be based on our recent development of the superhydrophobic-superhydrophilic micropatterning methods and the ability to create high-density arrays of droplet microreservoirs on superhydrophobic-superhydrophilic patterns that can be used for parallelized and miniaturized cell experiments.
Summary
Experiments with live cells are fundamentally important in biology, pharmaceutical industry, biotechnology or in medicine and diagnostics. One important example of cell experiments is the prescreening of cells from cancer biopsies with anticancer drugs in order to identify the most effective and least toxic combination of drugs for a particular patient also known as personalized medicine.
The goal of this ERC Proof-of-Concept project is to develop, fabricate and optimize a device (CellScreenChip) for performing miniaturized, parallel and, therefore, more affordable and faster cell screening experiments for the areas of diagnostics and personalized medicine. Applications of the CellScreenChip include (but not limited to) cell based disease diagnosis (e.g. cancer diagnostics), drug screening (e.g. body on a chip) or personalized medicine (e.g. personalized drug compatibility tests). The CellScreenChip will be based on our recent development of the superhydrophobic-superhydrophilic micropatterning methods and the ability to create high-density arrays of droplet microreservoirs on superhydrophobic-superhydrophilic patterns that can be used for parallelized and miniaturized cell experiments.
Max ERC Funding
150 000 €
Duration
Start date: 2015-10-01, End date: 2017-03-31
Project acronym chemos
Project Chemical Hematology: breaking resistance of hematological malignancies through personalized drug trials
Researcher (PI) Giulio Superti-Furga
Host Institution (HI) CEMM - FORSCHUNGSZENTRUM FUER MOLEKULARE MEDIZIN GMBH
Call Details Proof of Concept (PoC), ERC-2016-PoC, ERC-2016-PoC
Summary Personalized medicine aspires to provide optimal therapy in real-time during patient treatment, however current methodology falls short to deliver this in a robust manner. With this in mind, we invented a method for the screening of thousands of drug responses in small samples of an individual’s peripheral blood by automated microscopy and single-cell image analysis. We termed this method pharmacoscopy. In the course of carrying out the i-FIVE ERC grant project plan, we began screening for novel anti-viral or immune modulating drugs. In the quest to increase the physiological relevance of our screening settings, we investigated the possibility of using peripheral blood cells or bone marrow from individuals. We have thus far been able to show that the approach allows for the screening of anti-inflammatory properties of compounds, and to score for distinct sub-population specific cell cytotoxicity profiles of clinical anti-neoplastic agents through the tracking of fluorescent antibodies and probes. Moreover, we have been able to show that the approach empowers the therapeutic decision-making capability of hema-oncologists in a concrete clinical setting using primary myelofibrosis and lymphoma as test diseases. With funding from this grant, we intend to obtain further clinical data through retrospective trials, and incorporate the results into an information package attractive enough to draw the attention of potential investors. We have secured the intellectual property rights and have assembled the know-how required to enable commercialization efforts. With the unique image-based single cell analysis of human liquid tissues, we believe that chemos has the potential to develop into a service that enables and advances personalized medicine and drug discovery for a broad spectrum of hematological disorders.
Summary
Personalized medicine aspires to provide optimal therapy in real-time during patient treatment, however current methodology falls short to deliver this in a robust manner. With this in mind, we invented a method for the screening of thousands of drug responses in small samples of an individual’s peripheral blood by automated microscopy and single-cell image analysis. We termed this method pharmacoscopy. In the course of carrying out the i-FIVE ERC grant project plan, we began screening for novel anti-viral or immune modulating drugs. In the quest to increase the physiological relevance of our screening settings, we investigated the possibility of using peripheral blood cells or bone marrow from individuals. We have thus far been able to show that the approach allows for the screening of anti-inflammatory properties of compounds, and to score for distinct sub-population specific cell cytotoxicity profiles of clinical anti-neoplastic agents through the tracking of fluorescent antibodies and probes. Moreover, we have been able to show that the approach empowers the therapeutic decision-making capability of hema-oncologists in a concrete clinical setting using primary myelofibrosis and lymphoma as test diseases. With funding from this grant, we intend to obtain further clinical data through retrospective trials, and incorporate the results into an information package attractive enough to draw the attention of potential investors. We have secured the intellectual property rights and have assembled the know-how required to enable commercialization efforts. With the unique image-based single cell analysis of human liquid tissues, we believe that chemos has the potential to develop into a service that enables and advances personalized medicine and drug discovery for a broad spectrum of hematological disorders.
Max ERC Funding
146 668 €
Duration
Start date: 2016-10-01, End date: 2017-09-30
Project acronym CONMIC
Project Concrete micromolds for microinjection molding
Researcher (PI) Stephan Foerster
Host Institution (HI) UNIVERSITAET BAYREUTH
Call Details Proof of Concept (PoC), PC1, ERC-2015-PoC
Summary Microinjection molding is the current standard technology for the production of microcomponents. There is an increasing demand for microcomponents with feature sizes down to micrometers due to a general trend towards miniaturization in the medical and automotive industry. The main problem to meet this demand is the considerable fix-cost of the micromolds (microstructured injection tool inserts). Currently, the methods for their fabrication are lithography-based LIGA-techniques, electrical discharge machining (EDM), or precision laser ablation with high capital and maintenance costs.
Our goal is the development and commercialization of inorganic composite micromolds, which can be produced at significantly reduced costs, thus making microinjection molding more profitable and variable. We found that inorganic composites are surprisingly versatile material for this purpose. The amazing feature of these composite micromolds is their extremely smooth surface having sub-micron roughness, an exact replication of even micrometer size features, and their excellent stability. Lower fix costs for such micromolds allow microinjection molding also of smaller numbers of microparts for special demands, e.g. for medical applications, thus opening new markets for microinjection molding.
The proposed project aims to bring this idea to the proof-of-concept level by demonstrating a inorganic composite micromold that can be used in commercial microinjection molding equipment for the production of microcomponents. In parallel, we will also develop our future technical and intellectual property rights strategy, explore the market potential and secure potential customers. We finally intend to launch a company to develop the product and bring it to the market.
Summary
Microinjection molding is the current standard technology for the production of microcomponents. There is an increasing demand for microcomponents with feature sizes down to micrometers due to a general trend towards miniaturization in the medical and automotive industry. The main problem to meet this demand is the considerable fix-cost of the micromolds (microstructured injection tool inserts). Currently, the methods for their fabrication are lithography-based LIGA-techniques, electrical discharge machining (EDM), or precision laser ablation with high capital and maintenance costs.
Our goal is the development and commercialization of inorganic composite micromolds, which can be produced at significantly reduced costs, thus making microinjection molding more profitable and variable. We found that inorganic composites are surprisingly versatile material for this purpose. The amazing feature of these composite micromolds is their extremely smooth surface having sub-micron roughness, an exact replication of even micrometer size features, and their excellent stability. Lower fix costs for such micromolds allow microinjection molding also of smaller numbers of microparts for special demands, e.g. for medical applications, thus opening new markets for microinjection molding.
The proposed project aims to bring this idea to the proof-of-concept level by demonstrating a inorganic composite micromold that can be used in commercial microinjection molding equipment for the production of microcomponents. In parallel, we will also develop our future technical and intellectual property rights strategy, explore the market potential and secure potential customers. We finally intend to launch a company to develop the product and bring it to the market.
Max ERC Funding
149 213 €
Duration
Start date: 2016-07-01, End date: 2017-06-30
Project acronym CONQUEST
Project Companion Nanodiagnostics for Quantifying EPR and Stratifying Patients to Targeted Nanotherapies
Researcher (PI) Twan Gerardus Gertrudis Maria Lammers
Host Institution (HI) UNIVERSITAETSKLINIKUM AACHEN
Call Details Proof of Concept (PoC), ERC-2015-PoC, ERC-2015-PoC
Summary CONQUEST aims to commercialise a first-of-its-kind platform technology for imaging a biological effect – i.e. the EPR effect – that is predictive for a cancer patient's response to tumor-targeted nanomedicine (NM) therapy. CONQUEST thereby addresses a key issue in the (nano)pharmaceutical industry; as currently large proportions of cancer patients do not respond to NM, while others show major improvements in terms of response rates, survival times and quality of life. This trend impairs the outcome of clinical studies and results in many patients receiving treatments that are not effective to them. It would therefore be highly desirable to stratify responders from non-responders prior to study entry or treatment. CONQUEST stands at the basis of introducing a solution to this problem in the pharmaceutical industry.
Prof. Lammers and colleagues, as part of ERC-funded research, have developed a powerful imaging approach that allows to construct an EPR profile of each individual tumour - by the administration and non-invasive imaging of contrast agent-labelled nanocarriers (drug-loaded or empty) that accumulate in tumours through EPR. The general idea is that patients with a low degree of EPR, and therefore unlikely to respond to such treatments, can be excluded from NM treatment and referred to alternative established or experimental interventions. Vice versa, patients with a high level of EPR can likely be treated relatively efficiently.
Recognising the commercial potential of this technology, CONQUEST aims to tailor the technique and protocol for application in humans, by tuning the method for imaging with PET-MRI. A successful demonstration of PET-MRI-based EPR imaging will trigger large interest of the pharmaceutical and diagnostics industry, to invest in further clinical (co-) development.
Summary
CONQUEST aims to commercialise a first-of-its-kind platform technology for imaging a biological effect – i.e. the EPR effect – that is predictive for a cancer patient's response to tumor-targeted nanomedicine (NM) therapy. CONQUEST thereby addresses a key issue in the (nano)pharmaceutical industry; as currently large proportions of cancer patients do not respond to NM, while others show major improvements in terms of response rates, survival times and quality of life. This trend impairs the outcome of clinical studies and results in many patients receiving treatments that are not effective to them. It would therefore be highly desirable to stratify responders from non-responders prior to study entry or treatment. CONQUEST stands at the basis of introducing a solution to this problem in the pharmaceutical industry.
Prof. Lammers and colleagues, as part of ERC-funded research, have developed a powerful imaging approach that allows to construct an EPR profile of each individual tumour - by the administration and non-invasive imaging of contrast agent-labelled nanocarriers (drug-loaded or empty) that accumulate in tumours through EPR. The general idea is that patients with a low degree of EPR, and therefore unlikely to respond to such treatments, can be excluded from NM treatment and referred to alternative established or experimental interventions. Vice versa, patients with a high level of EPR can likely be treated relatively efficiently.
Recognising the commercial potential of this technology, CONQUEST aims to tailor the technique and protocol for application in humans, by tuning the method for imaging with PET-MRI. A successful demonstration of PET-MRI-based EPR imaging will trigger large interest of the pharmaceutical and diagnostics industry, to invest in further clinical (co-) development.
Max ERC Funding
145 312 €
Duration
Start date: 2016-01-01, End date: 2017-06-30
Project acronym CTCapture_2.0
Project Advanced platform for profiling of therapeutic targets and functional analysis of circulating tumour cells in cancer patients
Researcher (PI) Klaus Pantel
Host Institution (HI) UNIVERSITAETSKLINIKUM HAMBURG-EPPENDORF
Call Details Proof of Concept (PoC), PC1, ERC-2016-PoC
Summary As an alternative to invasive needle biopsies, the analysis of CTCs released by metastatic lesions into the blood has been recently introduced by the PI as “liquid biopsy”. The molecular analysis of CTCs before and during treatment could supply a real-time status of the landscape of metastatic tumor cell clones in an individual cancer patient. CTCs might reveal representative information on metastatic cells located at different sites because the blood represents a pool of tumor cells potentially released by all lesions in the cancer patients. Moreover, blood samples can be taken sequentially during the course of the disease and therefore allow a real-time assessment of the molecular evolution of the disease with important implications for decision making on cancer therapies. However, despite the obvious potential of CTCs as biomarker, current CTC capture assays require sophisticated, expensive and complex assay systems, which is the most important bottleneck for a more widespread use of CTCs as liquid biopsy. The assay development in the ERC PoC Grant CAPTURE-CTC (end: 11/2016) and the successful research on improved methods for molecular characterization of CTCs in the Advanced Investigator Grant DISSECT (end: 07/2016) of the PI has allowed to develop a novel improved platform for CTC detection. To implement our chip into future clinical decision making, we will now focus on the clinical validation of the chip platform including the development of SOPs as basis for kits for expression of therapeutic targets and resistance mechanisms in CTCs. Moreover, the establishment of transient CTC cultures from chip-isolated tumor cells will foster drug testing in individual cancer patients. In conclusion, the CTCapture_2.0 project will be an important prerequisite for successful future commercialization of a novel liquid biopsy assay.
Summary
As an alternative to invasive needle biopsies, the analysis of CTCs released by metastatic lesions into the blood has been recently introduced by the PI as “liquid biopsy”. The molecular analysis of CTCs before and during treatment could supply a real-time status of the landscape of metastatic tumor cell clones in an individual cancer patient. CTCs might reveal representative information on metastatic cells located at different sites because the blood represents a pool of tumor cells potentially released by all lesions in the cancer patients. Moreover, blood samples can be taken sequentially during the course of the disease and therefore allow a real-time assessment of the molecular evolution of the disease with important implications for decision making on cancer therapies. However, despite the obvious potential of CTCs as biomarker, current CTC capture assays require sophisticated, expensive and complex assay systems, which is the most important bottleneck for a more widespread use of CTCs as liquid biopsy. The assay development in the ERC PoC Grant CAPTURE-CTC (end: 11/2016) and the successful research on improved methods for molecular characterization of CTCs in the Advanced Investigator Grant DISSECT (end: 07/2016) of the PI has allowed to develop a novel improved platform for CTC detection. To implement our chip into future clinical decision making, we will now focus on the clinical validation of the chip platform including the development of SOPs as basis for kits for expression of therapeutic targets and resistance mechanisms in CTCs. Moreover, the establishment of transient CTC cultures from chip-isolated tumor cells will foster drug testing in individual cancer patients. In conclusion, the CTCapture_2.0 project will be an important prerequisite for successful future commercialization of a novel liquid biopsy assay.
Max ERC Funding
149 825 €
Duration
Start date: 2017-05-01, End date: 2018-10-31
Project acronym DeShield
Project Hide and Seek with Cancer Drugs
Researcher (PI) Wilfried WEBER
Host Institution (HI) ALBERT-LUDWIGS-UNIVERSITAET FREIBURG
Call Details Proof of Concept (PoC), PC1, ERC-2016-PoC
Summary Cancer is one of the most prominent causes for morbidity and mortality in industrialized countries. The key challenge in drug-based anti-cancer therapy is to efficiently kill the cancer cells while minimizing side-effects on healthy parts of the body. The DeShield project will establish the proof of concept for a novel approach to upgrade existing anti-cancer drugs in a way that the anti-cancer effect will be increased while side-effects will simultaneously minimized. DeShield technology will be used to shield approved anti-cancer drugs while circulating in the body in order to minimize side effects. Once the shielded drug accumulated at the cancer site, an external stimulus will be applied to trigger de-shielding. The drug will then locally and specifically be taken up by the cancer cells to exert its therapeutic effect. We have successfully demonstrated the functionality of the DeShield technology using the clinically approved anti-cancer drug Doxil and human cancer cell lines: when the shield is intact, the drug is not taken up by the cells, only upon inducible un-shielding the drug enters and kills the cells. In the DeShield project we aim at establishing the Proof-of-Concept that this approach is functional in cancer animal models, that it increases the therapeutic effect while minimizing side-effects. To this aim we have assembled a team with high expertise in complementary areas covering the technology itself, the conductance of preclinical animal studies up to clinical trials as well as business expertise. The technical advance obtained in this project together with a comprehensive market research and the development of a business strategy will shape a highly attractive commercial proposition for the successful valorization of our ERC-funded research.
Summary
Cancer is one of the most prominent causes for morbidity and mortality in industrialized countries. The key challenge in drug-based anti-cancer therapy is to efficiently kill the cancer cells while minimizing side-effects on healthy parts of the body. The DeShield project will establish the proof of concept for a novel approach to upgrade existing anti-cancer drugs in a way that the anti-cancer effect will be increased while side-effects will simultaneously minimized. DeShield technology will be used to shield approved anti-cancer drugs while circulating in the body in order to minimize side effects. Once the shielded drug accumulated at the cancer site, an external stimulus will be applied to trigger de-shielding. The drug will then locally and specifically be taken up by the cancer cells to exert its therapeutic effect. We have successfully demonstrated the functionality of the DeShield technology using the clinically approved anti-cancer drug Doxil and human cancer cell lines: when the shield is intact, the drug is not taken up by the cells, only upon inducible un-shielding the drug enters and kills the cells. In the DeShield project we aim at establishing the Proof-of-Concept that this approach is functional in cancer animal models, that it increases the therapeutic effect while minimizing side-effects. To this aim we have assembled a team with high expertise in complementary areas covering the technology itself, the conductance of preclinical animal studies up to clinical trials as well as business expertise. The technical advance obtained in this project together with a comprehensive market research and the development of a business strategy will shape a highly attractive commercial proposition for the successful valorization of our ERC-funded research.
Max ERC Funding
149 981 €
Duration
Start date: 2017-06-01, End date: 2018-11-30