GlycoMimetics Announces Results of Pivotal Phase 3 Study of Uproleselan in Relapsed/Refractory (R/R) Acute Myeloid Leukemia (AML)
06 Maggio 2024 - 12:00PM
Business Wire
- Study of uproleselan combined with chemotherapy did not meet
its primary endpoint of overall survival in the intent to treat
population
- Adverse events were consistent with known side effect profiles
of chemotherapy used in the study
- Comprehensive data analysis with medical, statistical, and
regulatory experts underway and will be shared as appropriate;
company will submit results for presentation at an upcoming medical
meeting
- National Cancer Institute (NCI) Phase 2/3 study in newly
diagnosed AML patients remains ongoing
- Conference call and webcast to be hosted today, May 6, 2024, at
8:30 a.m. ET.
GlycoMimetics, Inc. (Nasdaq: GLYC), a late clinical-stage
biotechnology company discovering and developing glycobiology-based
therapies for cancers and inflammatory diseases, today announced
topline results from its Phase 3 global pivotal study of
uproleselan in 388 patients with R/R AML. In the study, uproleselan
combined with chemotherapy did not achieve a statistically
significant improvement in overall survival in the intent to treat
population versus chemotherapy alone.
Patients treated with uproleselan had a median overall survival
of 13 months, compared to 12.3 months in the placebo arm. Adverse
events were consistent with known side effect profiles of
chemotherapy used in the study.
“While the outcome of our Phase 3 study in R/R AML is not what
we hoped, we wish to thank the investigators, the participating
patients and their families for their dedication to this large,
well-controlled randomized study,” said Harout Semerjian, Chief
Executive Officer of GlycoMimetics. “We are thoroughly analyzing
the data in collaboration with medical, statistical and regulatory
experts and are committed to submitting a comprehensive data
analysis for presentation at an upcoming medical meeting.”
The randomized, double-blind, placebo-controlled Phase 3
clinical study evaluated uproleselan in combination with MEC
(mitoxantrone, etoposide and cytarabine) or FAI (fludarabine,
cytarabine and idarubicin) in patients with R/R AML. Patients
received either uproleselan or placebo for 8 days over 1 cycle of
an induction and, if applicable, up to 3 cycles of consolidation.
The primary endpoint of the study was overall survival without
censoring for transplant. Secondary endpoints included incidence of
severe oral mucositis, complete remission rate and remission rate.
A total of 388 patients across 70 sites in nine countries were
randomized 1:1 between treatment and placebo arms.
The NCI and the Alliance for Clinical Trials in Oncology are
conducting an adaptive Phase 2/3 study of uproleselan in adults
with newly diagnosed AML who are 60 years or older and fit for
intensive chemotherapy. The randomized, controlled study is
evaluating the addition of uproleselan to a standard
cytarabine/daunorubicin regimen (7+3) versus chemotherapy alone.
The Phase 2 portion of the study completed enrollment of 267
patients in December 2021. Results of the pre-planned Phase 2 event
free survival interim analysis will be reported when available.
First Quarter 2024 Preliminary Financial Results
Today, the company also disclosed its preliminary financial
results for the first quarter of 2024.
- Cash position: As of March 31, 2024, GlycoMimetics had cash and
cash equivalents of $31.3 million, compared to $41.8 million as of
December 31, 2023.
- R&D Expenses: The company’s research and development
expenses increased to $6.0 million for the quarter ended March 31,
2024, as compared to $5.4 million for the same period in 2023.
These increases were due to raw material acquisition costs for
future manufacturing batches.
- G&A Expenses: The company’s general and administrative
expenses decreased to $5.1 million for the quarter ended March 31,
2024, compared to $5.5 million for the same period in 2023. The
decrease was due to lower personnel-related and external consulting
expenses.
- Shares Outstanding: Shares of common stock outstanding as of
March 31, 2024, were 64,450,835.
Conference Call Information
The company will host a conference call and webcast today at
8:30 a.m. ET. To access the call by phone, please go to this
registration link and you will be provided with dial in details.
Participants are encouraged to connect 15 minutes in advance of the
scheduled start time.
A live webcast of the call will be available on the “Investors”
tab on the GlycoMimetics website. A webcast replay will be
available for 30 days following the call.
Please note this call will replace the previously announced
First Quarter 2024 Financial Results call scheduled for May 9, 2024
at 8:30 a.m. ET.
About AML
AML is the most common acute leukemia in adults. A cancer of the
bone marrow, nearly 21,000 people in the United States are
diagnosed with AML each year. Despite the availability of multiple
treatments, disease prognosis is poor, and new treatment options
are needed to improve outcomes. Newly diagnosed AML has the lowest
5-year survival rate of all leukemias at 31.7%. The five-year
survival rate for people with relapsed/refractory disease is only
10%.
About Uproleselan
Discovered and developed by GlycoMimetics, uproleselan (yoo’ pro
le’se lan) is an investigational, first-in-class E-selectin
antagonist. GlycoMimetics has received Breakthrough Therapy and
Fast Track designations from the U.S. Food and Drug Administration
(FDA) and Breakthrough Therapy designation from the Chinese
National Medical Products Administration for uproleselan as a
potential treatment for adult AML patients with relapsed or
refractory disease. E-selectin is a leukocyte adhesion molecule
constitutively expressed on endothelial cells of the vasculature
and bone marrow. In AML, there is evidence that E-selectin–ligand
interaction between endothelial cells in the protective niche of
the Bone Marrow microEnvironment (BME) and leukemic stem cells and
blasts promotes leukemic cell survival and hides them from AML
therapies. Uproleselan is designed to disrupt E-selectin binding
and prevent leukemic myeloid cells using the protective niche of
the BME.
About GlycoMimetics, Inc.
GlycoMimetics is a late clinical-stage biotechnology company
discovering and developing glycobiology-based therapies for
cancers, including AML, and for inflammatory diseases. The
company’s scientific approach is based on an understanding of the
role that carbohydrates play in cell recognition. Its specialized
chemistry platform is being deployed to discover small molecule
drugs, known as glycomimetics, that alter carbohydrate-mediated
recognition in diverse disease states, including cancers and
inflammation. GlycoMimetics is leveraging its differentiated
expertise with this scientific approach in order to advance its
pipeline of wholly owned drug candidates. The company’s goal is to
develop transformative therapies for diseases with high unmet
medical need. GlycoMimetics is headquartered in Rockville, MD in
the BioHealth Capital Region. Learn more at
www.glycomimetics.com.
Forward-Looking Statements
This press release contains forward-looking statements. These
forward-looking statements may include, but are not limited to,
statements regarding the conduct of, and timing for analysis and
presentation of data from, clinical trials; potential development
and regulatory activities; and the potential benefits and impact of
uproleselan. Actual results may differ materially from those
described in these forward-looking statements. For a further
description of the risks associated with these statements, as well
as other risks facing GlycoMimetics, please see the risk factors
described in the company’s Annual Report on Form 10-K filed with
the U.S. Securities and Exchange Commission (SEC) on March 27,
2024, and other filings GlycoMimetics makes with the SEC from time
to time. Forward-looking statements speak only as of the date of
this release, and GlycoMimetics undertakes no obligation to update
or revise these statements, except as may be required by law.
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version on businesswire.com: https://www.businesswire.com/news/home/20240506092613/en/
Investor Contact: Argot
Partners Leo Vartorella 212-600-1902
Glycomimetics@argotpartners.com
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