Galapagos to Host KOL Event on December 10, 2023, at 11:00 AM PST
to discuss new data presented at ASH 2023
Mechelen, Belgium; 6 December 2023, 22:01 CET; Galapagos
NV (Euronext & NASDAQ: GLPG) today announced that it will host
a Key Opinion Leader (KOL) event during the 65th ASH Annual Meeting
& Exposition in San Diego, CA, on Sunday, December 10, 2023,
from 11:00 am PST to 12:30 pm PST. The in-person event will be held
at the San Diego Marriott Gaslamp Quarter in the Presidio Ballroom
B/C. To register as an in-person attendee, please
click here. To register as a virtual attendee,
please click here.
The event will feature the following KOLs who will review the
results observed to date of the ongoing Phase 1/2 CD19 CAR-T
studies with GLPG5201 (EUPLAGIA-1) and GLPG5101 (ATALANTA-1):
- Professor Matthew S. Davids, MD, MMSc – Associate Professor of
Medicine at Harvard Medical School, Director of Clinical Research,
Associate Director of the CLL Center
- Professor Paolo Ghia, MD, PhD – Professor of Medical Oncology,
Director, Strategic Research Program on CLL, Università Vita-Salute
San Raffaele, Milano, Italy
- Professor Sébastien Anguille – Head of Hematology, University
of Antwerp, Belgium
- Professor Michael R. Bishop, MD, FACP, FASCO – Director, The
David and Etta Jonas Center for Cellular Therapy, University of
Chicago
The event will also include a discussion of the potential for
CAR-T candidates, manufactured using the Galapagos Point-of-Care
platform, to improve survival for patients with a broad range of
B-cell malignancies. Galapagos leadership, including Paul
Stoffels1, MD, CEO and Chairman, will provide updates on:
- EUPLAGIA-1 study with GLPG5201 (CD19 CAR-T) in
relapsed/refractory chronic lymphocytic leukemia (rrCLL), with or
without Richter transformation (RT)
- ATALANTA-1 study with GLPG5101 (CD19 CAR-T) in
relapsed/refractory non-Hodgkin lymphoma (rrNHL)
A live question and answer will follow the formal presentations.
For more information, please contact sofie.vangijsel@glpg.com and
nathalie.siegel@glpg.com.
About Matthew S. Davids, MD, MMScAfter
obtaining an AB cum laude in chemistry at Harvard College, Dr.
Davids completed his MD cum laude at Yale University School of
Medicine. He served as an intern, resident, and assistant chief
resident in internal medicine at New York-Presbyterian Weill
Cornell Medical Center and Memorial Sloan-Kettering Cancer Center
in New York City. He then completed his fellowship in hematology
and oncology in Dana-Farber/Partners CancerCare, and a Master in
Medical Science (MMSc) at Harvard Medical School. He is an
attending physician in the Division of Lymphoma, where he serves as
the Director of Clinical Research, as well as Associate Director of
the CLL Center. He is also an Associate Professor of Medicine at
Harvard Medical School and attends on the inpatient hematologic
malignancies service at Brigham and Women's Hospital. Dr. Davids
has an active translational research program in CLL and non-Hodgkin
lymphoma, focusing on studying apoptosis (in particular Bcl-2
biology) in his laboratory, and leading clinical trials to evaluate
novel therapeutic strategies in patients with CLL and other
hematologic malignancies. Much of his work has focused on the
clinical development of new therapeutic regimens in CLL utilizing
combinations of targeted inhibitors of Bcl-2, B cell receptor
pathway kinases, and other novel agents, as well as utilizing
checkpoint blockade to enhance anti-tumor immunity in patients with
hematologic malignancies who relapse post allogeneic hematopoietic
cell transplantation.
About Paolo Ghia, MD, PhDPaolo Ghia received
his MD from the University of Torino, Italy, and received his PhD
working at the Basel Institute for Immunology, Switzerland,
studying B lymphocyte development. Next, he studied the molecular
mechanisms of the pathogenesis of chronic lymphoproliferative
disorders, particularly of follicular lymphoma at the Dana-Farber
Cancer Institute, Harvard Medical School, Boston.
He is now working in Milano, as Professor of Medical Oncology at
the Università Vita-Salute San Raffaele; and Director of the
Strategic Research Program on CLL, including a dedicated unit for
phase 1 studies, at the affiliated Ospedale San Raffaele.
His research interest is the study of the molecular and cellular
mechanisms acting in the natural history of Chronic Lymphocytic
Leukemia (CLL), including Monoclonal B-cell Lymphocytosis (MBL). On
these topics he has published over 350 manuscripts in peer-reviewed
journals.
He is President of the European Research Initiative on CLL
(ERIC) and a treasurer of the International Workshop on CLL
(iwCLL). He coauthors the EHA-ESMO guidelines for CLL treatment and
the ERIC recommendations on IGHV, TP53 and MRD analyses. He is
currently Associate Editor for CLL at Hemasphere, the official
Journal of the European Hematology Association (EHA).
About Sébastien Anguille, MD, PhDProf.
Sébastien Anguille (°1983 in Kapellen, Belgium) graduated summa cum
laude as medical doctor (MD) in 2008 at the University of Antwerp,
Antwerp, Belgium. After his graduation, Prof. Anguille joined the
research group of Prof. Zwi Berneman at the same institution as a
PhD student (supported by a 4-year FWO “aspirant” mandate and a
1-year “Emmanuel Van der Schueren” fellowship of the Flemish League
against Cancer to finish his PhD). His PhD thesis, which revolved
around cellular immunotherapy and more specifically around the
development of an optimized dendritic cell vaccine for acute
myeloid leukemia, resulted in several high-visibility publications
in renowned journals, including Blood, Leukemia, Proceedings of the
National Academy of Sciences, and Lancet Oncology. In 2012-2013,
Prof. Anguille spent a 6-month research visit to the Dendritic Cell
Biology & Therapeutics group of the ANZAC Research Institute in
Sydney, Australia, headed by the late Prof. Derek Hart. This
research stay abroad was supported by a FWO travel grant (V444212N)
and by a highly prestigious Endeavour Research Award granted by the
Australian Government.
In 2013, Prof. Anguille started his training as a medical
specialist in Internal Medicine, which he completed in 2016. He
qualified as Clinical Hematologist in 2017. Prof. Anguille works as
full-time staff member in the Division of Hematology of the Antwerp
University Hospital since 2016. Since January 1st, he succeeded
Prof. Zwi Berneman as Head of the Division of Hematology of the
Antwerp University Hospital and as Head of the Laboratory of
Experimental Hematology (LEH) of the Faculty of Medicine &
Health Sciences of the University of Antwerp.
In addition to his clinical activities, Prof. Anguille’s main
research focus continues to be on cellular immunotherapies for
hematological diseases, including cell-based cancer vaccines and
adoptive T-cell therapies (T-cell receptor [TCR]- and chimeric
antigen receptor [CAR]-engineered T cells). His research activities
involve both basic research (he is currently promotor or
co-promotor of 8 PhD students at LEH) as well as
translational/clinical research. Within this context, Prof.
Anguille serves as principal investigator (mainly in the field of
cellular immunotherapy) of several clinical trials running at the
Division of Hematology of the Antwerp University Hospital,
including two large, multicentric academic cell therapy trials in
hematological diseases for which he obtained funding from the
Belgian National Cancer Plan Action 29 (€1,500,000 €) and from Kom
op Tegen Kanker (€761,780). Prof. Anguille is co-chairing an
FWO-TBM project (awarded in 2020 for a total amount of 1 305 429 €)
together with Prof. Stroobants from the Molecular Imaging Center
Antwerp (MICA) of the University of Antwerp. Since 2021, he is also
promotor of an FWO Research Project entitled “BCMA immunoPET to
predict and monitor treatment response to CAR-based cellular
therapies in multiple myeloma” (€462,504). His research was awarded
with several national and international prizes and grants
(including a VOCATIO award in 2012, a FWO research grant in 2018, a
prize from the Horlait-Dapsens Foundation in 2018, a research grant
from Janssen Pharmaceutics in 2019, and the Gilead Belux Fellowship
2020). In 2019, Dr Anguille was one of the laureates of the FWO
“Fundamentele Klinische Mandaten”, enabling him to combine his
clinical activities with basis research on TCR- and CAR-engineered
T cells for hematological malignancies. To date, Prof. Anguille’s
research resulted in 158 publications with >4000 citations and a
Google scholar H-index of 33.
About Michael R. Bishop, MD, FACP, FASCODr.
Bishop is Professor of Medicine and the Director of the David and
Etta Jonas Center forCellular Therapy at the University of Chicago.
Dr. Bishop’s research focuses on the development and conduct novel
clinical trials in cellular therapy. His current research efforts
focus on the development and therapeutic use of T-cell therapies to
treat both hematologic malignancies and solid tumors. In addition,
his research program is focused on methods to prevent and treat
recurrent disease following transplantation and cellular therapy,
with a primary focus on B-cell malignancies.
About Galapagos
We are a global biotechnology company with
operations in Europe and the US dedicated to developing
transformational medicines for more years of life and quality of
life. Focusing on high unmet medical needs, we synergize the most
compelling science, technology, and collaborative approaches to
create a deep pipeline of best-in-class small molecules, CAR-T
therapies, and biologics in oncology and immunology. With
capabilities from lab to patient, including a decentralized,
point-of-care CAR-T manufacturing network, we are committed to
challenging the status quo and delivering results for our patients,
employees and shareholders. For additional information, please
visit www.glpg.com or follow us on LinkedIn or X (formerly
Twitter).
Contact
Media
inquiries:Marieke Vermeersch +32 479 490
603 media@glpg.com |
Investor
inquiries:Sofie Van Gijsel +1 781 296
1143ir@glpg.comSandra Cauwenberghs ir@glpg.com |
Forward-looking statementsThis press release
includes forward-looking statements within the meaning of the
Private Securities Litigation Reform Act of 1995, as amended. These
statements are often, but are not always, made through the use of
words or phrases such as “anticipate,” “expect, ” “plan,”
“estimate,” “will,” “continue,” “aim,” “intend,” “future,”
“potential,” “could,” ”indicate,” “forward,” as well as similar
expressions. Forward-looking statements contained in this release
include, but are not limited to, statements regarding preliminary,
interim and topline data from the EUPLAGIA-1 and ATALANTA-1
clinical studies with GLPG5201 and GLPG5101 and other analyses
related to CD19 CAR-T, statements related to Galapagos’ plans,
expectations and strategy with respect to the EUPLAGIA-1 and
ATALANTA-1 clinical studies with GLPG5201 and GLPG5101, and
statements regarding the expected timing, design and readouts of
the clinical studies with GLPG5201 and GLPG5101, including the
expected recruitment for trials. Forward-looking statements involve
known and unknown risks, uncertainties and other factors which
might cause our actual results to be materially different from
those expressed or implied by such forward-looking statements.
These risks, uncertainties and other factors include, without
limitation, the risk that preliminary or interim clinical results
may not be replicated in ongoing or subsequent clinical trials; the
risk that ongoing and future clinical studies with GLPG5201 and
GLPG5101 may not be completed in the currently envisaged timelines
or at all, the inherent uncertainties associated with competitive
developments, clinical trial and product development activities and
regulatory approval requirements (including that data from the
ongoing and planned clinical research programs may not support
registration or further development of GLPG5201 and GLPG5101 due to
safety, efficacy or other reasons), Galapagos' reliance on
collaborations with third parties (including its collaboration
partner Lonza) and that Galapagos’ estimations regarding its
GLPG5201 and GLPG5101 development programs and regarding the
commercial potential of GLPG5201 and GLPG5101, may be incorrect, as
well as those risks and uncertainties identified in Galapagos’
Annual Report on Form 20-F for the year ended 31 December 2022
filed with the U.S. Securities and Exchange Commission (SEC) and
its subsequent filings with the SEC. All statements other than
statements of historical fact are statements that could be deemed
forward-looking statements. The forward-looking statements
contained herein are based on management’s current expectations and
beliefs and speak only as of the date hereof, and Galapagos makes
no commitment to update or publicly release any revisions to
forward-looking statements in order to reflect new information or
subsequent events, circumstances, or changes in expectations.
1 Acting via Stoffels IMC BC
- Galapagos to Host KOL Event on December 10 2023, at 1100 AM PST
to discuss new data presented at ASH 2023
Grafico Azioni Galapagos (TG:GXE)
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Da Ott 2024 a Nov 2024
Grafico Azioni Galapagos (TG:GXE)
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Da Nov 2023 a Nov 2024