Humacyte Leadership to Present at Multiple Scientific Events in November
November 08 2021 - 6:30AM
Humacyte, Inc. (Nasdaq: HUMA), a clinical-stage biotechnology
platform company developing universally implantable bioengineered
human tissue at commercial scale, today announced that leadership
will present new data and additional information on its programs at
several scientific events in November 2021.
“Humacyte is creating off-the-shelf universally implantable
bioengineered human tissues to potentially transform the treatment
of chronic disease and injuries. We’re pleased to share data on
both our late- and early-stage development programs which
contribute to our understanding of the broad applicability of our
platform,” said Laura Niklason, M.D., Ph.D., Founder, President and
Chief Executive Officer of Humacyte. “Notably, we will share new
data on our LUNA200 commercial-scale manufacturing system, which is
our groundbreaking bioengineering platform for producing human
tissue at large scale. The advancement of the LUNA200 system
supports our efforts toward commercialization of our Human
Acellular Vessel (HAV). In addition, we will present the first data
from our pre-clinical primate work using a small diameter HAV as a
Blalock-Taussig (BT) shunt, to address congenital heart
defects.”
The details of the events are as follows:
Mayo Clinic Regenerative Medicine and Surgery
SymposiumSession: Advanced Biomanufacturing:
Considerations for Biologic TherapeuticsTitle: Innovations in
Tissue Engineering - A Promising New Potential for Patients The
presentation summarized Humacyte’s ongoing HAV development program
in vascular repair, reconstruction and replacement and potential
future applications.Location: Virtual webcastDate / time: Friday,
Nov. 5, 2021, 9:05-9:20 a.m. MDTPresenter: Juliana Blum, Ph.D.,
Co-founder and Executive Vice President of Corporate Development,
Humacyte
Session: Advanced Biomanufacturing: Considerations for Biologic
TherapeuticsTitle: The Human Acellular Vessel (HAV) as a Vascular
Implant for Limb Salvage: A Mayo FDA Collaborative Under Expanded
Access IND ProvisionsThe presentation highlighted the successful
implantation of Humacyte’s HAV to restore blood circulation in the
leg of a patient suffering from severe peripheral arterial disease,
completed at Mayo Clinic under an expanded access approval by the
U.S FDA. Location: Virtual webcastDate / time: Friday, Nov. 5,
2021, 9:20-9:35 a.m. MDTPresenter: Col. Todd E. Rasmussen, M.D.,
Professor and Senior Associate Consultant, Division of Vascular and
Endovascular Surgery, Mayo Clinic
American Heart Association Scientific Sessions
2021Session: Therapeutic Cells, Genes, and Drugs for
Cardiovascular TranslationTitle: Evaluation of Tissue Engineered
Human Acellular Vessels as a Blalock-Taussig-Thomas Shunt in a
Juvenile Primate ModelA presentation of new preclinical data on the
development of Humacyte’s small diameter HAV for use as a BTT shunt
in pediatric heart disease. Location: Virtual webcast Date / time:
Monday, Nov. 15, 2021, 11 a.m. – 12 p.m. ESTPresenter: Kevin Nash,
Ph.D., Preclinical Scientist, Humacyte
6th World Congress of the Tissue Engineering and
Regenerative Medicine International Society
(TERMIS2021)Session: Keynote—Industry Day Session 3:
Innovation from idea to market in regenerative medicine Title:
Industrialization of Regenerative MedicineThe one-year safety and
efficacy data from the Phase 2 study of Humacyte’s HAVs
manufactured using the in-house commercial manufacturing system,
LUNA200, will be reported for the first time.Location: Virtual
webcastDate / time: Monday, Nov. 15, 2021, 3:30-5 p.m. CET /
10:30-11 a.m. ESTPresenter: Laura Niklason, M.D., Ph.D., Founder,
President and Chief Executive Officer, Humacyte
Session: In Vivo Animal Models and Clinical TrialsTitle: Safety,
Efficacy, and Immunogenicity Assessment of Humacyte’s Human
Acellular Vessel for Dialysis Vascular Access: LUNA SystemAn
overview of the Humacyte’s commercial-scale manufacturing system,
LUNA200, capable of producing ~40,000 HAVs annually, and data from
the Phase 2 study of HAVs manufactured using the LUNA200 system,
will be discussed. Location: Virtual webcastDate / time: Wednesday,
Nov. 17, 2021, 12 p.m. CET / 7 a.m. ETPresenter: Justin Strader,
Senior Process Engineer, Humacyte
About HAVHuman Acellular Vessels (HAV) are
engineered off-the-shelf replacement vessels initially being
developed for vascular repair, reconstruction and replacement. HAV
is intended to overcome long-standing limitations in vessel tissue
repair and replacement – it can be manufactured at commercial
scale, it eliminates the need for harvesting a vessel from a
patient, and clinical evidence suggests that it is non-immunogenic,
infection-resistant, and can become durable living tissue. HAV is
currently being evaluated in two Phase 3 trials in AV access and a
Phase 2/3 trial for vascular trauma, and has been used in more than
460 patient implantations. It is the first product to receive
Regenerative Medicine Advanced Therapy (RMAT) designation from the
U.S. Food and Drug Administration, and has also received FDA Fast
Track designation.
About HumacyteHumacyte, Inc., (Nasdaq: HUMA) is
developing a disruptive biotechnology platform to deliver
universally implantable bioengineered human tissues and organs
designed to improve the lives of patients and transform the
practice of medicine. The Company develops and manufactures
acellular tissues to treat a wide range of diseases, injuries and
chronic conditions. Humacyte’s initial opportunity, a portfolio of
human acellular vessels (HAVs), is currently in late-stage clinical
trials targeting multiple vascular applications, including vascular
trauma repair, arteriovenous access for hemodialysis, and
peripheral arterial disease. Pre-clinical development is also
underway in coronary artery bypass grafts, pediatric heart surgery,
treatment of type 1 diabetes, and multiple novel cell and tissue
applications. Humacyte’s HAVs were the first product to receive the
FDA’s Regenerative Medicine Advanced Therapy (RMAT) expedited
review designation and received priority designation for the
treatment of vascular trauma by the U.S. Secretary of Defense. For
more information, visit www.Humacyte.com.
Humacyte Investor
Contact:investors@humacyte.com
Humacyte Media Contact: media@humacyte.com
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