IN8bio Doses First Patient in Phase 2 Clinical Trial of INB-400 in Newly Diagnosed Glioblastoma
30 Aprile 2024 - 12:05PM
IN8bio, Inc. (Nasdaq: INAB), a clinical-stage biopharmaceutical
company advancing innovative gamma-delta T cell therapies,
announced today that the first patient in its Phase 2 clinical
trial evaluating INB-400 in patients with newly diagnosed
glioblastoma multiforme (GBM) has been successfully dosed at the
Cleveland Clinic in Ohio.
INB-400 is the Company’s first autologous
gamma-delta T cell therapy product candidate genetically engineered
to survive chemotherapy and maintain the natural ability to
recognize, engage and kill cancer cells when dosed along with
current, standard-of-care treatments such as temozolomide (Temodar,
or TMZ). Arm A of the INB-400 trial is expected to enroll up to 40
patients. INB-400 was granted Orphan Drug Designation by the FDA in
2023.
“The initiation of patient dosing in our Phase 2
trial of INB-400 represents an important milestone for both IN8bio
and patients with newly diagnosed GBM who have limited therapeutic
options,” said William Ho, CEO and co-founder of IN8bio. “Our novel
approach combines engineered, chemotherapy-resistant gamma-delta T
cells with standard-of-care treatments to potentially drive deeper
responses and improved patient outcomes in difficult-to-treat
cancers. We look forward to advancing INB-400 at multiple leading
medical centers across the United States for patients with GBM and
sharing updates, including long-term follow up data from the Phase
1 INB-200 program, at medical meetings this year.”
Gamma-delta T cells are naturally occurring
immune cells with unique properties enabling them to naturally
differentiate between healthy and cancerous tissues. They serve to
bridge between the innate and adaptive immune system, contributing
to direct tumor cell killing as well as immune memory, cell
recruitment and activation to drive deeper immune responses.
The Phase 2 study will evaluate the safety and
tolerability of INB-400 in patients with newly diagnosed GBM in
combination with TMZ. In Arm A of the trial, investigators will
administer T cells to patients on the first day of each of six
28-day maintenance cycles concurrent with TMZ for up to six doses.
The primary endpoint of the study is overall survival rate at 12
months. Secondary endpoints include safety and tolerability,
overall response rate, time to progression, and progression-free
survival.
Since 2005, the standard-of-care treatment for
GBM has been surgical resection followed by radiation and
chemotherapy and six cycles of maintenance temozolomide therapy,
referred to as the Stupp regimen. Most patients relapse in six to
seven months, with very few patients surviving beyond five years.
INB-400 is engineered to be resistant to alkylating chemotherapy,
enabling it to be used in combination with the current
standard-of-care TMZ to amplify immune signals, maximize tumor
killing, and eliminate cancer cells.
More information about the Phase 2 study
(NCT05664243) can be found at www.clinicaltrials.gov.
About INB-400
INB-400 is IN8bio’s DeltEx chemotherapy
resistant autologous drug-resistant immunotherapy (DRI). INB-400
was granted Orphan Drug Designation for the treatment of
glioblastoma multiforme (GBM) by the FDA in April 2023, marking the
first genetically modified gamma-delta T cell therapy to receive
this regulatory designation. GBM remains a significant unmet need,
treatment options and associated outcomes for GBM, highly
aggressive and difficult-to-treat brain cancer, have remained
largely unchanged for more than 18 years, with a median progression
free survival of 6-7 months and overall survival of 14-16 months.
Allogeneic INB-400 will expand the application of DRI gamma-delta T
cells into other solid tumor types through the development of
allogeneic or “off-the-shelf” DeltEx DRI.
About IN8bio
IN8bio is a clinical-stage biopharmaceutical
company developing gamma-delta T cell-based immunotherapies for
cancer patients. Gamma-delta T cells are a specialized population
of T cells that possess unique properties, including the ability to
differentiate between healthy and diseased tissue. The company’s
lead program INB-400 is in a Phase 2 trial in glioblastoma
multiforme (GBM). Additional programs include Phase 1 trials in
solid and hematologic tumors, including INB-200 for GBM and INB-100
for patients with hematologic malignancies undergoing
transplantation. For more information about IN8bio, visit
www.IN8bio.com.
Company Contact
IN8bio, Inc.
Patrick McCall+1 646.600.6GDT (6438)info@IN8bio.com
Investors
Meru AdvisorsLee M. Sternlstern@meruadvisors.com
Media Contact
Kimberly HaKKH
Advisors917.291.5744kimberly.ha@kkhadvisors.com
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