NextCure Reports Preclinical Data for LNCB74 and Additional Clinical Biomarker Data for NC410 Combo at Society for Immunotherapy of Cancer Annual Meeting
05 Novembro 2024 - 6:05PM
NextCure, Inc. (Nasdaq: NXTC), a clinical-stage
biopharmaceutical company committed to discovering and developing
novel, first-in-class and best-in-class therapies to treat cancer,
today reports pre-clinical data from LNCB74, a B7-H4-targeting
antibody-drug conjugate (ADC) being developed in partnership with
LigaChem Biosciences (LCB) (KOSDAQ: 141080), and biomarker data
from the NC410 combination study with pembrolizumab in patients
with immune checkpoint inhibitor (ICI) naïve and refractory
microsatellite stable (MSS)/microsatellite instability-low (MSI-L)
colorectal cancer (CRC). The data will be presented during poster
sessions at the Society for Immunotherapy of Cancer (SITC) annual
meeting.
“The preclinical data reported for LNCB74, our B7-H4
antibody-drug conjugate program, continue to reinforce its promise
as a potential best-in-class therapeutic with advantages over other
B7-H4 ADCs,” said Michael Richman, NextCure’s president and CEO.
“We remain on track to submit an IND application to the FDA by
year-end and intend to rapidly advance the program into clinical
development.”
Preclinical Data on LNCB74 B7-H4 Antibody Drug Conjugate
(ADC)
LNCB74 is a B7-H4 antibody conjugated to the microtubule
disrupting payload monomethyl auristatin E (MMAE) with a
drug-to-antibody ratio of 4 (DAR4). The ADC employs a
glucuronidase-cleavable, site-specific linkage conjugated to an
engineered cysteine in the antibody light chain via LigaChem
Biosciences’ ConjuAllTM technology to increase stability in
circulation, improve selective release of payload in tumor cells,
and reduce payload release in non-tumor cells. LNCB74 incorporates
an Fc mitigating mutation to minimize binding and uptake of LNCB74
by Fc receptor expressing immune cells. The ConjuAll technology,
with its selective cleavage and release within tumor cells,
combined with mitigation of off-target uptake via disabled Fc
interactions, is engineered to improve the safety profile and
therapeutic index of LNCB74 compared to other B7-H4 targeted
ADCs.
Key findings:
- B7-H4 protein is highly expressed in multiple tumor
indications. B7-H4 expression limited in normal healthy human
tissues, providing a potential broad therapeutic index for a B7-H4
targeting ADC.
- LNCB74 shows specific binding to B7-H4 expressing tumor cells
and is rapidly internalized in a target-dependent manner by cancer
cells.
- LNCB74 mediates potent cytotoxicity, with sub-nanomolar to low
nanomolar EC50 values on multiple B7-H4-positive cancer cell
lines.
- LNCB74 demonstrates strong anti-tumor activity in multiple CDX
and PDX tumor models. A single dose of 3 mg/kg resulted in durable
tumor regression in multiple tumor models, suggesting activity
comparable or superior to published B7-H4 targeting ADCs.
- LNCB74 demonstrates favorable PK and stability in rodents.
- LNCB74 was well tolerated in cynomolgus monkeys up to 10
mg/kg.
Phase 1b Study of NC410 in Combination with
Pembrolizumab
The presentation includes additional clinical data for CRC
patients from the Phase 1b portion of a Phase 1b/2 study evaluating
NC410, a LAIR-2 fusion protein, in combination with pembrolizumab.
The trial is evaluating the combination in ovarian cancer and
ICI-naïve MSS/MSI-L CRC. Overall, the combination of NC410 and
pembrolizumab continues to demonstrate clinical activity against
MSS/MSI-L CRC, which is generally unresponsive to immunotherapy.
Subjects who achieved clinical benefit of partial response or
stable disease demonstrated durability of their responses that was
clinically meaningful in this patient population.
Key findings:
- Of the 43 evaluable ICI-naïve MSS/MSI-L CRC patients without
liver metastasis, there were 3 PRs as of the data cut-off of
October 14, 2024.
- Disease control rates were 86% and 47% for the 200 mg and 100
mg NC410 doses, respectively.
- Biomarker data support proposed mechanism of action of NC410,
showing remodeling of the tumor microenvironment, promotion of
immune infiltration and anti-tumor activity.
- Treatment was well tolerated.
Poster Presentation Details:
Title: LNCB74 is a B7-H4 antibody-drug
conjugate with a β-glucuronide linker-MMAE payload system to
enhance therapeutic index in B7-H4 expressing cancersLead
Author: Shannon M. KahanAbstract Number:
1051Session Date & Time: Friday, November 8,
2024, 5:30 – 7:00 PM
Title: NC410 in combination with pembrolizumab
improves anti-tumor responses by promoting collagen remodeling and
tumor immunity in advanced ICI naive MSS/MSI-L CRCLead
Author: Alina BarbuAbstract Number:
632Session Date & Time: Saturday, November 9,
2024, 7:10 – 8:30 PM
About NextCure, Inc.
NextCure is a clinical-stage biopharmaceutical company that is
focused on advancing innovative medicines that treat cancer
patients that do not respond to, or have disease progression on,
current therapies, through the use of differentiated mechanisms of
actions including antibody-drug conjugates, antibodies and
proteins. We focus on advancing therapies that leverage our core
strengths in understanding biological pathways and biomarkers, the
interactions of cells, including in the tumor microenvironment, and
the role each interaction plays in a biologic
response. http://www.nextcure.com
Cautionary Statement Regarding Forward-Looking
Statements
Statements made in this press release that are not historical
facts are forward-looking statements. Words such as “expects,”
“believes,” “intends,” “hope,” “forward” and similar expressions
are intended to identify forward-looking statements.
Forward-looking statements involve substantial risks and
uncertainties that could cause actual results to differ materially
from those projected in any forward-looking statement. Such risks
and uncertainties include, among others: our limited operating
history and no products approved for commercial sale; our history
of significant losses; our need to obtain additional financing;
risks related to clinical development, including that early
clinical data may not be confirmed by later clinical results; risks
that pre-clinical research may not be confirmed in clinical trials;
risks related to marketing approval and commercialization; and
NextCure’s dependence on key personnel. More detailed information
on these and additional factors that could affect NextCure’s actual
results are described in NextCure’s filings with the Securities and
Exchange Commission (the “SEC”), including NextCure’s most recent
Form 10-K and subsequent Form 10-Q. You should not place undue
reliance on any forward-looking statements. NextCure assumes no
obligation to update any forward-looking statements, even if
expectations change.
Investor InquiriesTimothy Mayer, Ph.D.NextCure,
Inc.Chief Operating Officer(240) 762-6486IR@nextcure.com
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