LAVA Therapeutics to Present Updated Data from the Phase 1/2a Clinical Trial of LAVA-051 at the 64th American Society of Hematology (ASH) Annual Meeting and Exposition
03 Noviembre 2022 - 7:00AM
LAVA Therapeutics N.V. (Nasdaq: LVTX), a clinical-stage
immuno-oncology company focused on developing its proprietary
Gammabody™ platform of bispecific gamma delta T cell engagers to
transform the treatment of cancer, today announced the Company will
present updated data including safety, pharmacodynamics and
pharmacokinetics from the ongoing Phase 1/2a clinical trial of
LAVA-051 during the 64th American Society of Hematology (ASH®)
Annual Meeting and Exposition, taking place in New Orleans,
Louisiana and virtually December 10-13, 2022. First data from
subcutaneous administration will be presented, along with updates
on the intravenous dosing-cohorts.
The details of the poster presentation session are as
follows:
Abstract #: 2014Abstract
Title: LAVA-051, a Novel Bispecific Gamma-Delta
T-Cell Engager (Gammabody), in Relapsed/Refractory MM and CLL:
Pharmacodynamic and Early Clinical DataSession
Name: Cellular Immunotherapies: Early Phase and
Investigational Therapies: Poster ISession #:
704Session Date: Saturday, December 10,
2022Session Time: 5:30 p.m.–7:30 p.m.
ESTPresenter: Arnon P. Kater, M.D., Ph.D.,
chairman of the Dutch/Belgium HOVON CLL working group and professor
of translational hematology at the Amsterdam University Medical
Center
About LAVA TherapeuticsLAVA Therapeutics N.V.
is a clinical-stage immuno-oncology company utilizing its
proprietary Gammabody™ platform to develop a portfolio of
bispecific gamma delta T cell engagers for the potential treatment
of solid and hematologic malignancies. The Company utilizes
bispecific antibodies engineered to selectively kill cancer cells
by triggering Vγ9Vδ2 (Vgamma9 Vdelta2) T cell antitumor effector
functions upon cross-linking to tumor-associated antigens.
LAVA-051, the Company’s lead candidate for the treatment of
multiple myeloma, chronic lymphocytic leukemia, and acute myeloid
leukemia, is enrolling patients in a Phase 1/2a clinical study
(NCT04887259). A Phase 1/2a clinical study to evaluate LAVA-1207 in
patients with metastatic castration-resistant prostate cancer
(mCRPC) is also enrolling (NCT05369000). For more information,
please visit www.lavatherapeutics.com, and follow us
on LinkedIn, Twitter and YouTube.
LAVA’s Cautionary
Note on
Forward-Looking StatementsThis
press release contains forward-looking statements, including with
respect to the company’s anticipated growth and clinical
development plans, including the timing of clinical trials. Words
such as “anticipate,” “believe,” “could,” “will,” “may,” “expect,”
“should,” “plan,” “intend,” “estimate,” “potential” and similar
expressions (as well as other words or expressions referencing
future events, conditions or circumstances) are intended to
identify forward-looking statements. These forward-looking
statements are based on LAVA’s expectations and assumptions as of
the date of this press release and are subject to various risks and
uncertainties that may cause actual results to differ materially
from these forward-looking statements. Forward-looking statements
contained in this press release include, but are not limited to,
statements about the preclinical data, clinical development and
scope of clinical trials, and the potential use of our product
candidates to treat various tumor targets. Many factors, risks and
uncertainties may cause differences between current expectations
and actual results including, among other things, the timing and
results of our research and development programs and preclinical
and clinical trials, our ability to obtain regulatory approval for
and commercialize our product candidates, our ability to leverage
our initial programs to develop additional product candidates using
our Gammabody™ platform, and the failure of LAVA’s collaborators to
support or advance collaborations or our product candidates. The
COVID-19 pandemic may disrupt our business and that of the third
parties on which we depend, including delaying or otherwise
disrupting our clinical trials and preclinical studies,
manufacturing and supply chain, or impairing employee productivity.
In addition, there may be adverse effects on our business condition
and results from general economic and market conditions and overall
fluctuations in the United States and international equity markets,
including deteriorating market conditions due to investor concerns
regarding inflation and hostilities between Russia and Ukraine.
LAVA assumes no obligation to update any forward-looking statements
contained herein to reflect any change in expectations, even as new
information becomes available.
CONTACTSInvestor
Relationsir@lavatherapeutics.com
Argot Partners (IR/Media)212-600-1902lava@argotpartners.com
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