Affimed Announces Acceptance of Three Abstracts at the 2024 ASH Annual Meeting Including an Oral Presentation Underscoring Advancing Clinical Pipeline in Leukemia and Lymphoma
05 Noviembre 2024 - 8:00AM
Affimed N.V. (Nasdaq: AFMD) (“Affimed”, or the “Company”), a
clinical-stage immuno-oncology company committed to giving patients
back their innate ability to fight cancer, today announced three
abstracts on two of its innate cell engagers (ICE®) are accepted
for presentation at the 66th ASH Annual Meeting and Exposition
taking place December 7-10, 2024, in San Diego, California. An oral
presentation will feature clinical results including promising
efficacy and safety data from the AFM28 phase 1 dose escalation
study in relapsed/refractory acute myeloid leukemia (AML). A poster
with preclinical data will highlight the in vitro efficacy of AFM28
in combination with both patient-derived autologous NK cells and
healthy volunteer-derived allogeneic NK cells against leukemic
blasts.
Updated clinical results from all 4 cohorts of the run-in phase
from the LuminICE-203 study evaluating acimtamig (AFM13) in
combination with AlloNK® (AB-101) for relapsed/ refractory Hodgkin
Lymphoma will be shared in a poster session.
Details for the oral presentation and poster sessions are as
follows:
Abstract Title |
Date / Time / Presenter |
Session Name / Location |
“Investigating the Novel Combination of the Innate Cell Engager
(ICE®) Acimtamig with Off-the-Shelf Allogeneic Natural Killer Cells
AlloNK® in Relapsed or Refractory Classical Hodgkin Lymphoma (R/R
cHL): Initial Results of the Phase 2 Luminice-203 Study” |
December 8, 2024 6:00 PM - 8:00 PM PTJoseph Maakaron, MDDivision of
Hematology, Oncology and Transplantation, Department of Medicine,
Masonic Cancer Center, University of Minnesota, Minneapolis, MN,
USA |
- Session Name: 624. Hodgkin Lymphomas: Clinical and
Epidemiological: Poster II
- Location: San Diego Convention Center, Halls G-H
- Publication Number: 3052
|
“Engaging Innate Immunity by AFM28, an Innate Cell Engager (ICE®)
Targeting CD123-Positive Leukemic Cells in Patients with
Relapsed/Refractory Acute Myeloid Leukemia: Safety and Efficacy
Results of a First-in-Human Phase 1 Study” |
December 9, 2024 10:30 AM - 12:00 PM PTOral Presentation Time:
11:45 AM PTPau Montesinos, MD, PhDHospital Universitari i
Politècnic La Fe, Valencia, Spain |
- Session Name: 616. Acute Myeloid Leukemias: Investigational
Drug and Cellular Therapies: New Treatment Approaches for AML
- Room: Manchester Grand Hyatt San Diego, Grand Hall B
|
“The Bispecific Innate Cell Engager AFM28 Can Leverage AML
Patient’s NK Cells in Addition to Allogeneic NK Cells, Enabling
Elimination of CD123+ Leukemic Stem and Progenitor Cells in AML and
MDS” |
December 9, 2024 6:00 PM - 8:00 PM PTNanni Schmitt, Dr. sc.
hum.Department of Hematology and Oncology, Medical Faculty
Mannheim, Heidelberg University, Mannheim, Germany |
- Session: 604. Molecular Pharmacology and Drug Resistance:
Myeloid Neoplasms: Poster III
- Location: San Diego Convention Center, Halls G-H
|
The abstracts are available online at the 66th ASH Annual
Meeting and Exposition – Hematology.
The final oral presentation and clinical poster will be
available after the congress on Affimed’s website at Publications
& Posters.
About Acimtamig
Acimtamig (AFM13) is a first-in-class ICE® that uniquely
activates the innate immune system to destroy CD30-positive
hematologic tumors. Acimtamig induces specific and selective
killing of CD30-positive tumor cells, leveraging the power of the
innate immune system by engaging and activating natural killer (NK)
cells and macrophages. Acimtamig is a tetravalent bispecific innate
cell engager designed to act as a bridge between the innate immune
cells and the tumor, creating the necessary proximity for the
innate immune cells to destroy the tumor cells.
About LuminICE-203 (AFM13-203)
LuminICE-203 (AFM13-203) is a Phase 2 open-label, multicenter,
multi-cohort study. The trial is evaluating the safety and efficacy
of the combination of acimtamig (AFM13) with Artiva
Biotherapeutics’ allogeneic NK cell AlloNK® (AB-101) in patients
with relapsed/refractory classical Hodgkin lymphoma and
CD30-positive peripheral T cell lymphoma (NCT05883449).
The study builds on the unprecedented efficacy results from an
investigator sponsored study, AFM13-104, which investigated
acimtamig in combination with cord blood-derived NK cells in
patients with refractory/recurrent CD30-positive Hodgkin or
non-Hodgkin lymphoma (NCT04074746).
About AFM28
AFM28, a tetravalent, bispecific CD123- and
CD16A-binding ICE®, is designed to bring our immunotherapeutic
approach to patients with acute myeloid leukemia (AML). It engages
NK cells to initiate tumor cell killing via antibody-dependent
cellular cytotoxicity, even at low CD123 expression levels. AFM28
is currently in clinical development as monotherapy in patients
with AML (NCT05817058).
About AFM28-101
AFM28-101 is a first-in-human Phase 1 open-label, nonrandomized,
multicenter, multiple ascending dose escalation study evaluating
AFM28 monotherapy in patients with relapsed/refractory
CD123-positive AML (NCT05817058).
About Affimed N.V.
Affimed (Nasdaq: AFMD) is a clinical-stage immuno-oncology
company committed to giving patients back their innate ability to
fight cancer by actualizing the untapped potential of the innate
immune system. The Company’s innate cell engagers (ICE®) enable a
tumor-targeted approach to recognize and kill a range of
hematologic and solid tumors. ICE® are generated on the Company’s
proprietary ROCK® platform which predictably generates customized
molecules that leverage the power of innate immune cells to destroy
tumor cells. A number of ICE® molecules are in clinical
development, being studied as mono- or combination therapy.
Headquartered in Mannheim, Germany, Affimed is led by an
experienced team of biotechnology and pharmaceutical leaders united
by the bold vision to stop cancer from ever derailing patients’
lives. For more about the Company’s people, pipeline and partners,
please visit: www.affimed.com.
Forward-Looking Statements
This press release contains forward-looking statements. All
statements other than statements of historical fact are
forward-looking statements, which are often indicated by terms such
as “anticipate,” “believe,” “could,” “estimate,” “expect,” “goal,”
“intend,” “look forward to,” “may,” “plan,” “potential,” “predict,”
“project,” “should,” “will,” “would” and similar expressions.
Forward-looking statements appear in a number of places throughout
this release and include statements regarding the Company’s
intentions, beliefs, projections, outlook, analyses and current
expectations concerning, among other things, the potential of
acimtamig (AFM13), AFM24, AFM28 and the Company’s other product
candidates; the value of its ROCK® platform; its ongoing and
planned clinical trials; its corporate restructuring, the
associated headcount reduction and the impact this may have on
Company’s anticipated savings and total costs and expenses; its
collaborations and development of its products in combination with
other therapies; the timing of and its ability to make regulatory
filings and obtain and maintain regulatory approvals for its
product candidates; its intellectual property position; its
collaboration activities; its ability to develop commercial
functions; clinical trial data; its results of operations, cash
needs, financial condition, liquidity, prospects, future
transactions, growth and strategies; the industry in which it
operates; the macroeconomic trends that may affect the industry or
the Company, such as the instability in the banking sector
experienced in the first quarter of 2023; impacts of the COVID-19
pandemic, the benefits to Affimed of orphan drug designation; the
impact on its business by political events, war, terrorism,
business interruptions and other geopolitical events and
uncertainties, such as the Russia-Ukraine conflict; the fact that
the current clinical data of acimtamig in combination with NK cell
therapy is based on acimtamig precomplexed with fresh allogeneic
cord blood-derived NK cells from The University of Texas MD
Anderson Cancer Center, as opposed to Artiva’s AB-101; and other
uncertainties and factors described under the heading “Risk
Factors” in Affimed’s filings with the SEC. Given these risks,
uncertainties, and other factors, you should not place undue
reliance on these forward-looking statements, and the Company
assumes no obligation to update these forward-looking statements,
even if new information becomes available in the future.
Investor Relations
Alexander FudukidisDirector, Investor
RelationsE-Mail: a.fudukidis@affimed.comTel.: +1 (917)
436-8102
Media Contact
Mary Beth Sandin Vice President, Marketing and
CommunicationsE-Mail: m.sandin@affimed.com
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