In vivo detection of CTCs in head and neck cancer patients using the GILUPI CellCollector®
GILUPI GmbH announces the recent publication of a clinical study demonstrates the isolation of circulating tumor cells (CTCs) from blood of squamous cell carcinoma of head and neck (SCCHN) patients with the GILUPI CellCollector® .
Isolating and analyzing CTCs from the blood of cancer patients can provide additional information on prognosis, course of disease, treatment efficacy and molecular tumor evolution. CTC detection is challenging due to their extremely low frequency amongst millions of leucocytes and billions of red blood cells. Especially in SCCHN, the sensitivity of CTC isolation with conventional in vitro methods is low and insufficient to satisfy clinical requirement. Zhang and further colleagues from the Nanjing Tongren Hospital in China wanted to overcome this limitation by using the in vivo GILUPI CellCollector® technology. Therefore, from November 2016 to April 2017 the clinicians enrolled 22 newly diagnosed SCCHN patients as well as 9 healthy volunteers.
Published data are already available for CTC isolation using the GILUPI CellCollector® technology in patients with prostate cancer, neuroendocrine tumors, metastatic breast and lung cancer with high positivity rates (54 – 97%). In addition, this Chinese study revealed for the first time, a high incidence of CTCs in patients with squamous cell carcinoma of head and neck. In total, 72.7% (16/22) were positive for >= 1 CTC (range 1-17 cells). The CTC detection rate was higher in patients with late stages than in patients with early stages. More importantly, CTC number changes as a marker for analyzing surgical response was tested. Zhang et al. showed that positivity rate decreases from 72.7% with median CTC number of 2 before surgical treatment to 46.7% with median CTC number of 0 after surgical treatment. Moreover, the expression of a therapy relevant oncogene (EGFRVIII) was detected on CTCs and this positive expression was also found in both primary and metastatic tumor tissue. These data revealed that an in vivo detection of CTCs had high sensitivity in SCCHN, which might improve CTC application in clinic.
 Zhang et al. "Enumeration and molecular characterization of circulating tumor cell using an in vivo capture system in squamous cell carcinoma of head and neck.” Chin J Cancer Res. 2017 Jun;29(3):196-203. doi: 10.21147/j.issn.1000-9604.2017.03.05.
Detection of circulating tumor cells in breast cancer patients using the GILUPI CellCollector®
GILUPI GmbH announces that a scientific article about a multicenter, clinical trial in China has been published in the current issue of "National Medical Journal of China". The scientific paper demonstrates the isolation of circulating tumor cells (CTCs) from blood of breast cancer patients with the GILUPI CellCollector® .
Isolating and analyzing CTCs from the blood of cancer patients can provide additional information on prognosis of patients, treatment efficacy and molecular tumor evolution. Li and further colleagues from four different cancer centers in China investigated the prognostic relevance of CTCs in metastatic breast cancer (MBC). For this purpose the unique and innovative GILUPI CellCollector® in vivo technology was included in this clinical trial.
From April to August 2016, 127 patients diagnosed with metastatic breast cancer and 63 patients diagnosed with benign breast disease were enrolled. MBC patients received a GILUPI CellCollector® application before treatment and approximately 4 weeks after starting treatment, while benign patients had one GILUPI CellCollector® application.
Published data are already available for CTC isolation using the GILUPI CellCollector® technology in patients with prostate cancer, neuroendocrine tumors and lung cancer with high positivity rates (54 – 97%). In addition, this chinese study revealed for the first time, a high incidence of CTCs in newly progressive metastatic breast cancer patients. In metastatic breast cancer group 74.8% were positive for CTCs and the number of CTC detected in the benign group was 0 in each case. More importantly, CTC rates detected by the GILUPI CellCollector® displayed a decrease after 4 weeks treatment to 45% positivity rate. Li et al., showed also that the captured CTCs could be characterized on a molecular level. In conclusion, the researchers revealed a high specificity and sensitivity of CTCs as prognostic value.
 Li et al. " Circulating tumor cells in patients with breast tumors were detected by a novel device: a multicenter, clinical trial in China”, Zhonghua Yi Xue Za Zhi. 2017 Jun 27;97(24):1857-1861. doi: 10.3760/cma.j.issn.0376-2491.2017.24.003. Article in Chinese; For English version please contact GILUPI
Zulassung für Potsdamer Medizinprodukt in China
Der GILUPI CellCollector® - das erste zugelassene Medizinprodukt zur in vivo – Isolation von zirkulierenden Tumorzellen der Potsdamer GILUPI GmbH hat im Juni die Zulassung durch die Chinesische Zulassungsbehörde (CFDA) erhalten. Damit eröffnet sich für das Potsdamer Unternehmen einer der bedeutendsten geographischen Märkte weltweit. Dieser Meilenstein konnte in enger Zusammenarbeit mit dem Chinesischen Vertriebspartner, der Hebei Viroad Biotechnology Co. Ltd. (kurz „ Viroad") erreicht werden. Viroad ist auch zugleich größter Investor in dem Potsdamer Unternehmen.
„Viroad ist für uns ein ausgezeichneter Partner, denn auf Basis der hervorragenden Marktkenntnisse sowie der regulatorischen Expertise von Viroad ist es gelungen, diese für uns besonders wichtige Zulassung zu erreichen. Damit verbunden erwarten wir ein deutliches Umsatzwachstum in den kommenden Jahren.“ kommentiert Alexander Herrmann, Geschäftsführer der GILUPI GmbH.
Die wichtige Rolle von Viroad für das brandenburgische Unternehmen GILUPI unterstrichen auch Brandenburgs Wirtschaftsstaatssekretär Hendrik Fischer und der Geschäftsführer der Wirtschaftsförderung Brandenburg (WFBB), Sebastian Saule, im Rahmen der aktuellen Delegationsreise nach China. Sie besuchten heute (06.07.) Xu Baozhi, die Geschäftsführerin des chinesischen Investors und Vertriebspartners, Hebei Viroad, in Shijiazhuang, der Hauptstadt von Brandenburgs Partnerprovinz Hebei. Dabei sagte Staatssekretär Fischer: „Die Wirtschaftsbeziehungen zu China sind für Brandenburg sehr wichtig. Wir freuen uns, dass mit GILUPI nun ein Brandenburger Unternehmen auf dem chinesischen Gesundheitsmarkt für Furore sorgt.“ WFBB-Geschäftsführer Saule erklärte: „Das ist eine neue Qualität in den Brandenburger Außenwirtschaftsbeziehungen zu China und stärkt zugleich den Gesundheitsstandort Brandenburg. Das ist ein schöner Erfolg der gemeinsamen Bemühungen in China und in Brandenburg, die Entwicklung des Unternehmens zu unterstützen.“
GILUPI extends its patent portfolio
- Second Chinese patent was granted in March 2017
GILUPI GmbH announced today that the company was granted a further Chinese patent protecting the unique and innovative GILUPI technology.
The patent (ZL201180024406.8), short titled “biodetector” is valid until 15 March 2031. The newly granted Chinese patent extends GILUPIs patent portfolio protecting next device generations with enhanced sensitivity and greater convenience for patients.
“The extension of our intellectual property into the Chinese market is important for our strategic orientation. It further significantly broadens our patent portfolio, protecting our proprietary GILUPI technology on a global scale” said Dr. Jens Pfannkuche, CEO of GILUPI GmbH.
GILUPI´s patent portfolio consist of 11 patent families and further patent applications that are currently subject to examination procedures for a number of inventions. Hence, further granted patents will follow soon.
Improved detection of circulating tumor cells in prostate cancer patients using the GILUPI CellCollector® in combination with two blood-based assays
GILUPI GmbH announces the release of clinical data from a prostate cancer clinical study in December 2016. The scientific paper demonstrates the isolation of circulating tumor cells (CTCs) from blood of non-metastatic high-risk prostate cancer patients with the GILUPI CellCollector® .
Liquid biopsy - isolating and analyzing circulating tumor cells (CTCs) from the blood of prostate cancer patients - can provide additional information on prognosis of patients, treatment efficacy and molecular tumor evolution. Prof. Klaus Pantel, Dr. Kuske and further researchers from the department of tumor biology at the University Medical Center Hamburg-Eppendorf investigated the prognostic relevance of CTCs in non-mestastatic prostate cancer. The goal of this study was to increase the sensitivity of CTC detection in patients with high-risk prostate cancer through the combination of three complementary assays. For this purpose the unique and innovative GILUPI CellCollector® in vivo technology was included in this study.
Peripheral blood was analyzed directly before and 3 month after radical prostatectomy to assess early dynamics in CTC counts. In total, 86 and 52 patients were enrolled before radical prostatectomy and 3 month after surgery, respectively.
In this clinical trial, combined application of the different CTC detection technologies revealed for the first time, a high incidence of CTCs in non-metastatic high-risk prostate cancer patients. Moreover, the researcher showed that the usual restriction of analyzing large blood volumes from cancer patients could be circumvented by GILUPI CellCollector® application, which resulted in equal or higher incidences CTC detection as comparator systems. More importantly, CTC rates detected by the GILUPI CellCollector® displayed a statistically significant decrease after surgery (66% to 34%, p = 0.031). These data revealed that after radical prostatectomy a reduced number of EpCAM-positive CTCs circulate in the blood stream, which is likely owed to the fact that the primary tumor as a major source of CTCs had been removed.
 Kuske et al. "Improved detection of circulating tumor cells in non-metastatic high-risk prostate cancer patients.”, Scientific Reports, 2016 Dec 21; 6:39736. doi: 10.1038/srep39736. eCollection 2016.
Chinesischer Biotechnologie-Investor VIROAD übernimmt GILUPI
Die Investoren AURELIA, High-Tech Gründerfonds (HTGF), KfW, ILB, der Risikokapitalfonds der Sparkassen des Landes Brandenburg und Business Angels veräußern ihre Anteile an der GILUPI GmbH – ein Unternehmen der therapiebegleitenden Krebsdiagnostik aus Potsdam - an den strategischen Partner VIROAD. Damit erhält GILUPI die Möglichkeit, die Entwicklung ihrer Medizinprodukte fortzuführen und ihre Produktpalette durch in-vitro Diagnostika zu diversifizieren. Gleichzeitig ermöglicht die Transaktion dem jungen Biotechnologieunternehmen den Zutritt zum attraktiven chinesischen Markt.
VIROAD ist bereits seit Dezember 2012 strategischer Partner, größter Investor und Gesellschafter der GILUPI. Der chinesische Investor hat langjährige Erfahrungen bei der Zulassung von Medizinprodukten. Das Zulassungsverfahren inklusive der dazu gehörigen klinischen Studien für den GILUPI CellCollector® hat in China bereits begonnen. Der GILUPI CellCollector® dient der Gewinnung von kompletten zirkulierenden Tumorzellen (CTC) – der sogenannten Flüssigbiopsie bzw. „liquid biopsy“. Um dem Unternehmen eine gesicherte Zukunft und Wachstumsperspektiven in internationalen Märkten zu geben, übernimmt VIROAD nun sämtliche Unternehmensanteile. Die Investoren, die GILUPI seit 2006 finanziell und unternehmerisch begleiten, freuen sich über den attraktiven Exit. Der HTGF, der als Seedinvestor den Start der GILUPI ermöglichte, hebt hervor, dass „durch das chinesische Engagement auch der Standort in Deutschland gestärkt und ausgebaut wird. VIROAD möchte die Produkte in China vertreiben, benötigt aber den deutschen Standort für die Weiterentwicklung und das Europageschäft“, so Dr. Michael Brandkamp, Geschäftsführer des HTGF.
Der GILUPI-Geschäftsführer Jens Pfannkuche ist überzeugt, dass das Unternehmen jetzt seine vielversprechende Technologie und weitere Diagnostikprodukte vor allem in Europa und Asien vermarkten kann: „Die prädiktive und therapiebegleitende Diagnostik wird im Bereich der Onkologie immer wichtiger, da es vielfältige Therapieoptionen und Medikamente gibt. Gemeinsam mit VIROAD können wir nun einen zügigen Marktzugang in China neben den Kernmärkten Europas umsetzten. Unser derzeitiger Schwerpunkt liegt auf den Möglichkeiten der Zellzählung als prognostischer Biomarker in den wesentlichen onkologischen Indikationen. Und wir arbeiten derzeit an molekularen Testverfahren, um genetische Veränderungen auf Ebene der DNA und RNA in den CTC für therapieentscheidende Maßnahmen v.a. im nicht-kleinzelligen Lungenkarzinom (NSCLC) zu identifizieren. Die leichtere Verfügbarkeit von CTC aus dem Blutstrom -im Vergleich zur Gewebsbiopsie- insbesondere zum Nachweis von Resistenzmutationen lässt die sogenannte „Liquid Biopsy“ attraktiv erscheinen.“
Xu Baozhi, General Manager des chinesischen Medizintechnikkonzerns VIROAD, hebt hervor: „Die Produkte der GILUPI stoßen in unserem chinesischen Markt auf eine große Nachfrage. Die Bevölkerung in unserem Land wird immer älter und der Markt für die Diagnostik wächst dynamisch. Wir freuen uns daher die Zusammenarbeit mit unserem deutschen Partner ausbauen zu können.“
GILUPI at the 17th World Conference on Lung Cancer
GILUPI will participate at the 17th World Conference on Lung Cancer (WCLC) in Vienna, Austria. The WCLC is the world’s largest meeting dedicated to lung cancer and other thoracic malignancies. The meeting will take place from 4th to 7th December with more than 7.000 participants expected.
Liquid biopsy - isolating and analyzing circulating tumor cells (CTCs) from the blood of cancer patients - can provide additional information on prognosis of patients, treatment efficacy, resistance and molecular tumor evolution. Dr. Julia Herrmann, clinician at the SRH Wald-Klinikum Gera - a certified lung cancer center (DKG), will present first data from a clinical trial using the GILUPI CellCollector®, to monitor CTC counts before and after surgery in non-small cell lung cancer (NSCLC) patients. The CTCs were further characterized on a molecular level. First results from 20 patients show that CTCs were isolated independent from tumor stages and could even be detected in quite early cases. Moreover, the difference between CTC occurrence before and after surgery suggested the possibility to identify patients responding to therapy or patients with stable disease.
The poster presentation will take place on Monday the 5th December in Hall B between 2.30 pm and 3.45 pm (abstract ID 5975). You are invited to meet Dr. Julia Herrmann as well as Dr. Jens Pfannkuche (CEO, GILUPI GmbH) and Dr. Julia Schulz (GILUPI, R&D division), which will also participate at this poster session.
GILUPI at the 6th Herbsttreffen AG Molekularpathologie
At the 6th Herbsttreffen AG Molekularpathologie in Karlsruhe, Germany, from 21th to 22th November 2016, GILUPI will be one of the exhibitors and sponsors of the event. The medical device company will be presenting its current product, the GILUPI CellCollector®, to an interested audience.
Liquid biopsy - isolating and analyzing circulating tumor cells (CTCs) from the blood of cancer patients - can provide additional information on prognosis of patients, treatment efficacy, resistance and molecular tumor evolution. Whereas CTCs represent the liquid phase of current tumor progression, cell free tumor DNA is apoptotic/necrotic cell material representing past cell death. CTC detection is challenging due to their extremely low frequency amongst millions of leucocytes and billions of red blood cells. The advanced GILUPI technology allows for the detection and characterization of CTCs combined with the proof of the malignant origin of the cells. The tumor cells are captured in vivo with high sensitivity and selectivity providing compelling and improved diagnostic use for personalized medicine, early diagnostic and clinical monitoring.
You are invited to visit our exhibition booth at the 6th Herbsttreffen AG Molekularpathologie. For further information on this congress, see here
About GILUPI GmbH
GILUPI GmbH is a medical device company founded in 2006 with focus on the development and production of innovative products for the in vivo isolation of rare cells from the blood circulation. Currently, the main focus of GILUPI is the diagnostics market for cancer.
Individual oncological targeted therapies become increasingly important in personalized medicine. The identification of the right drug for the individual patient is todays challenge in clinical practice. To address this medical need, the GILUPI CellCollector® is used to enrich rare cells by immune capture - i.e. directly "fishing" of CTCs in the patient's bloodstream. This methodology has proven to yield highest cell numbers and patient positivity rates in various cancer types. Applying diagnostic analyses ranging from immunostaining, DNA- and RNA-based methods, the isolated cells can be characterized and/or analyzed down to a molecular level.
The GILUPI CellCollector® is the first in vivo CTC isolation product worldwide that is CE approved.
For further information visit www.gilupi.com
Enumeration and molecular characterization of circulating tumor cells in prostate cancer patients using the GILUPI CellCollector®
GILUPI GmbH announces the release of clinical data from a prostate cancer setting in August 2016. The scientific paper demonstrate the isolation of circulating tumor cells (CTCs) from blood of prostate cancer patients with GILUPI CellCollector®.
Liquid biopsy - isolating and analyzing circulating tumor cells (CTCs) from the blood of prostate cancer patients - can provide additional information on prognosis of patients, treatment efficacy and molecular tumor evolution. Dr. Gerit Theil and further researcher from the Martin Luther University Halle-Wittenberg wanted to investigate the use of the GILUPI CellCollector® - in a proof of concept study. After in vivo isolation, CTCs underwent enumeration and characterization using molecular methods.
The researcher tested the functionality of the GILUPI CellCollector® in a preclinical step. They studied blood samples of 43 prostate cancer patients by applying the medical devices ex vivo.
Detection of CTCs in all tumor stages could be shown. The mean CTC count was 4.6 CTCs in patients with localized prostate cancer, 16.8 CTCs in patients with locally advanced prostate cancer, and 26.8 CTCs in patients with metastatic prostate cancer. More importantly, it could be shown that there was a significant difference in the cancer-specific survival rates. Patients with CTC counts < 5 CTCs had significant longer survival rates than patients with more than 5 CTCs. Furthermore, Theil et al. demonstrated that the captured CTCs could be characterized on a molecular level. The investigators detected tumor-associated transcripts of epidermal growth factor receptor (EGFR) and prostate-specific membrane antigen (PSMA) in patients with metastatic PCa in 42.8% and 14.3% of the analyzed samples, respectively. The above data was generated to demonstrate to the Federal Institute for Drugs and Medical devices (Germany, BfArM) the safe and effective use prior to in vivo application of the GILUPI CellCollector® in this indication. Further studies are ongoing to validate this finding as further diagnostic tool in the treatment of patients with prostate tumors.
The scientific paper entitled "The Use of a New CellCollector to Isolate Circulating Tumor Cells from the Blood of Patients with Different Stages of Prostate Cancer and Clinical Outcomes - A Proof-of-Concept Study.” by Theil et al., was published in PLoS One., 11(8):e0158354. doi: 10.1371/journal.pone.0158354. eCollection 2016. (1th August 2016).
Identification and enumeration of Circulating tumor cells in neuroendocrine tumor patients with GILUPI CellCollector®
GILUPI GmbH announces, that in August 2016 a published scientific paper demonstrated for the first time circulating tumor cell (CTCs) isolation in neuroendocrine tumor patients with GILUPI CellCollector®.
Isolating and analyzing circulating tumor cells as a “liquid biopsy” can be an additional source of diagnosis, prognosis, evaluation of treatment efficacy and molecular tumor evolution and metastatic sites. CTCs have been, so far, identified in patients with metastatic neuroendocrine tumor (NET) using a comparator method with limited sampling volume that leads to the detection of low frequency CTC numbers. Professor Tim Meyer and his group from the UCL Cancer Institute, University College London wanted to overcome this limitation and increases CTCs numbers by using the GILUPI CellCollector®.
In their study, the researcher used the GILUPI CellCollector® and the comparator method. In total, 34 patients with metastatic NET were enrolled and the GILUPI CellCollector® was used to isolate CTCs in vivo.
Applying the GILUPI CellCollector® in 33 of 34 NET patients CTCs were found with a median of 6 CTCs. In comparison, in only 16 of 34 NET patients with a median of 0 CTC could be detected with the comparator method. More importantly, the researcher investigated the prognostic relevance of CTC count with GILUPI CellCollector®. Using a cut-off of 7 CTCs, the progression free survival of patients with less than or equal 7 CTCs was in median 11 months compared to patients with more than 7 CTCs had a significantly lower progression free survival. Further studies are needed to validate this finding to potentially aid the treatment of patients with neuroendocrine tumors.
The scientific paper entitled "A comparison of CellCollector with CellSearch in patients with neuroendocrine tumors by Mandair et al., was published in Endocrine-Related Cancer, pii: ERC-16-0201. PMID:27521132 (12th August 2016).
GILUPI GmbH Receives ISO 13485 Certification for Manufacturing and Distribution of Cell Separation Devices
After the 68th AACC Annual Scientific Meeting & Clinical Lab Expo (AACC), GILUPI GmbH announces that it has received EN ISO 13485 certification for its German operations. This ISO 13485 certification is an important milestone in the development of the GILUPI GmbH medical device and downstream in vitro diagnostics (IVD) business, particularly in the fields of liquid biopsy, molecular diagnostics and clinical oncology.
Dr. Jens Pfannkuche, Managing Director of the GILUPI GmbH, commented: “This is an important step forward for the further growth of our business. Our ISO 13485 certification now allows us to seek market clearance and approval for our liquid biopsy CE-marked medical devices in regulated markets and to manufacture in vitro diagnostic kits for downstream molecular diagnostics. Our lead product, the GILUPI CellCollector® Detektor CANCER01 is already being adopted in clinical practice to accumulate circulating tumor cells (CTCs) in the European Union. Together with our partner company Hebei Viroad Biotechnology Co., Ltd. located in China, we are also very excited about achieving Chinese Food and Drug (CFDA) clearance in the near future for oncology use. The certification enables us to fully leverage our current and future B2B channels in Pharma and Diagnostics by broadening their trail protocols and product labels including CTCs next to cell-free tumor DNA and FFPE tissue for their oncology and product pipeline. We expect the emergence of future IVD molecular diagnostic kits referring to our CTC enrichment device due to increased sensitivity for downstream mutation analysis and subsequent selected therapies.”
GILUPI Strengthens Executive Team - Appoints Dr. Jens Pfannkuche as General Manager
GILUPI GmbH, a developer and manufacturer of medical devices to enrich circulating tumor cells (CTCs) in the human blood stream, announces that Dr. Jens Pfannkuche has been appointed to the position as General Manager of the GILUPI GmbH effective July 2016.
Previously, Dr. Pfannkuche worked in research and development, regulatory affairs, clinical studies, business development and licensing in the medical device industry including B.R.A.H.M.S - part of Thermo Fisher Scientific. Most recently, he served in various functions at B.R.A.H.M.S - part of Thermo Fisher Scientific and as Vice President Clinical Business Development and Regulatory Affairs at BRUKER Daltonik GmbH, where he carried global responsibility for the IVD product line regarding the clinical business development and licensing and the regulatory market access. Dr. Pfannkuche also led the MALDI mass spectrometry Imaging business entering the clinical pathology market. Dr. Pfannkuche studied Biology at the University of North West Wales /UK and University of Otago / NZ and did his doctoral thesis in vibrational spectroscopy at the Polish Academy of Science. He has more than 15 years of experience in the field of implantable medical devices and in vitro diagnostic products in ophthalmology, oncology, infectiology and cardiovascular indications, and has been active in global clinical development and business-to-business licensing and deal-making projects with global medical device and IVD companies.
“I am proud to be part of GILUPI and to enable leveraging GILUPIs potential in liquid biopsy technology for the clinical, industrial and research markets”, says Jens Pfannkuche. “In light of my experience and network in the diagnostic industry regarding break-through technology, I foresee that GILUPI will play a major role in the growing circulating tumor cell market to serve patients with less invasive, cost effective diagnostic solutions in the near future. I would like to thank the shareholders for their trust and I am looking forward to fully utilize the commercial potential of GILUPI in this attractive and growing market“.
First Chinese and further European patent for GILUPI were granted in 2016
GILUPI detection device for in vivo and/or in vitro enrichment of sample
GILUPI GmbH announced today, that the company received the first Chinese and another European patent protecting the unique and innovative GILUPI technology.
The Chinese patent (ZL201080027208.2) as well as the European patent (EP2442726 B1) titles “detection device for in vivo and/or in vitro enrichment of sample material” describes a functionalized structured medical wire for the accumulation of sample material. The device comprising a biocompatible polymer and a functional surface equipped with detection receptors which for example enables the isolation of cells directly from the blood of patients (in vivo). This patented technology is already being used in clinical settings on national and international level.
The recently received patents are an important supplementation of GILUPI`s intellectual property portfolio. Thus, the company has a broad and strong intellectual property position required to run the GILUPI businesses. GILUPI has filed further patent applications that are currently subject to examination procedures for a number of inventions, hence further granted patents will follow soon.
Führungswechsel bei der GILUPI GmbH
Alexander Herrmann übernimmt die Leitung des Medizintechnik-Unternehmens
Als neuer Managing Director verantwortet Alexander Herrmann ab sofort die Leitung des in Potsdam und Greifswald ansässigen Unternehmens. Er tritt damit die Nachfolge von Dr. Klaus Lücke an, der sich nach 10 Jahren neuen Herausforderungen außerhalb der GILUPI GmbH stellen möchte. Der diplomierte Betriebswirt Alexander Herrmann (43) verfügt über langjährige Erfahrungen in der Unternehmensführung von Biotechnologie-Unternehmen und soll die Vermarktung des GILUPI CellCollector® sowie den notwendigen Umbau des Unternehmens beschleunigen.
„Mit dem GILUPI CellCollector® verfügen wir über ein einzigartiges Produkt. Ziel der kommenden Monate wird es sein, die Anwendung des GILUPI CellCollector® um molekular-diagnostische Auswertungen zu ergänzen und damit für unsere Kunden noch wertvoller zu machen. Außerdem soll die Produktion am Standort Greifswald ausgebaut und unser Team um zusätzliche Experten ergänzt werden“, so Alexander Herrmann.
GILUPI ist Partner im europäischen Konsortium „CANCER-ID“ zur Validierung Blut-basierter Krebs-Biomarker
Blood-based biomarkers such as circulating tumor cells (CTCs), circulating free tumor DNA (cfDNA) and microRNAs (miRNAs) are established indicators of tumor burden in cancer patients. Assessment of these markers from blood provides an invaluable tool for modern cancer therapy.
In addition to being of high importance when biopsies of the original tumor are not accessible, blood-based liquid biopsy tests allow for close follow-up of disease markers to monitor treatment efficacy and potentially improve the choice of treatment options.
CANCER-ID is a newly formed European consortium funded by the Innovative Medicines Initiative (IMI) comprised of 33 partners from 13 countries focused on establishment of standard protocols and clinical validation of blood-based biomarkers (EGFR and HER2) in NSCLC and HER2-therapy resistant metastatic breast cancer.
The consortium brings together experts from academic and clinical research, innovative Small-to-Medium sized Enterprises (SMEs), diagnostics companies and the pharmaceutical industry - thus providing a unique setting for expanding the clinical utility of liquid biopsies. The project is supported by a substantial budget of EUR 14.5 million provided by industry partners (8.2 million EUR) as well as the IMI Joint Undertaking (EUR 6.3 million).
The academic leads of the CANCER-ID consortium are Prof. Klaus Pantel, Head of the Department of Tumor Biology at the University Medical Center Hamburg-Eppendorf, Germany, and Prof. Leon Terstappen, Head of the Department of Medical Cell Biophysics at the University of Twente, The Netherlands. Both are leaders in the field and have an impressive track record in basic research and applied science including device development. The EFPIA lead companies of the CANCER-ID consortium are Bayer HealthCare and Silicon Biosystems, a Menarini Group Company.
Klaus Luecke, founder of GILUPI commented: “This project is a major step for GILUPI, as it will demonstrate the superior performance of GILUPI technology in the isolation of CTCs for testing and monitoring of cancer patients. The isolation and subsequent characterization of blood-based biomarkers will become increasingly important as a method to monitor disease progression and therapy response. We believe that the liquid biopsy approach - with less-invasive and more frequent testing - will soon become part of the clinical routine for the benefit of a wide range of cancer patients.
GILUPI Investor Hebei Viroad Biotechnology Co. Ltd. eröffnet ca. 2000 m² Büro- und Laborräumlichkeiten in Shijiazhuang für die GILUPI CellCollector® Produktion in China
Ray of hope for pancreatic cancer care
Erfolgreiche Kooperation mit EKF Diagnostics Holdings (Irland) zur Detektion von genet. Mutationen
Erstmalige molekulare Mutationsanalyse von in vivo isolierten CTCs
Neue Server-Infrastruktur für GILUPI in Potsdam und Greifswald
Bildnachweis: GILUPI GmbH, Fujitsu Technologies, "microscope" by University of Liverpool Faculty of Health & Life Sciences
GILUPI wurde für den Brandenburger Zunkunftspreis CAI in der Kategorie "Innovation" nominiert.
GILUPI im TV
Die GILUPI GmbH wurde im Rahmen einer Präsentation von innovativen Firmen im Bundesland Mecklenburg-Vorpommern im Greifswald TV (Wirtschaftsfenster MV) vorgestellt.
Anlässlich der offiziellen Eröffnung der GILUPI GmbH-Zweigniederlassung in Greifswald (Mecklenburg-Vorpommern) strahlte der Norddeutsche Rundfunk (NDR) einen Kurzbeitrag aus.