Autonomix Medical, Inc. (NASDAQ: AMIX) (“Autonomix” or the
“Company”), a medical device company focused on advancing precision
nerve-targeted treatments, today highlighted positive preliminary
results from the first five “lead-in” patients in the Company’s
ongoing proof-of-concept human clinical trial (the “Trial”)
evaluating the safety and effectiveness of delivering transvascular
energy to ablate relevant problematic nerves and mitigate pain in
patients with pancreatic cancer pain. Three patients were treated
with femoral access and two were treated with brachial access.
Patients treated with brachial access showed no improvement in
their pain scores (or worsened) while all patients treated with
femoral access positively responded to treatment. The results
presented here reflect the three patients in the responder group.
Data, as previously reported, show a reduction in pain assessed
using the Visual Analog Scale (“VAS”) from a mean pre-procedure
score of 8.0 to a mean score of 1.33 at 4-6 weeks post-procedure.
Additionally, all responding patients were able to completely
eliminate their opioid use at 4-6 weeks post-procedure. The Trial
is expected to complete enrollment by year-end 2024.
“Late-stage pancreatic cancer patients with
chronic pain are often dependent on opioids, resulting in
significant side effects with risk of addiction and opioid
overdose,” commented Brad Hauser, Chief Executive Officer of
Autonomix. “Preliminary data from responding subjects in our
ongoing first-in-human trial have demonstrated a substantial,
sustained reduction in pain scores that eliminated the need for
opioid drugs for these patients. This underscores a potential
breakthrough in interventional pain management, and we look forward
to continuing evaluations of our differentiated approach and
providing meaningful benefit to patients.”
Opioid‐based pharmacotherapy is currently the
primary strategy used to manage moderate and severe pain for
patients with progressive and advanced pancreatic cancer.2
Additionally, as sited in the manuscript titled “Pancreas
Cancer‐Associated Pain Management”3, several reports have
established that cancer‐related pain affects patient survival in
pancreatic and other cancers.4,5,6,7 Inadequately treated pain can
significantly affect a patient's eligibility and tolerance for
chemotherapy. Conversely, patients with less pain intensity and
pain of shorter duration are reported to have a better quality of
life and longer survival.8,9
The Company’s first-in-class technology platform
utilizes a catheter-based microchip sensing array antenna that has
the ability to detect and differentiate neural signals with up to
3,000 times greater sensitivity than currently available
technologies. Once target nerves are identified, Autonomix uses its
proprietary radio frequency (RF) ablation technology to kill
targeted nerves, enabling a precision guided sense, treat and
verify approach to addressing a number of disease categories from
chronic pain management to hypertension and cardiology. Current
approaches, primarily relying on opioids or invasive ethanol
injections, can provide only limited relief and may lead to risky
side effects. For more information about the Company’s technology,
please visit autonomix.com.
About the Trial
The goal of the Trial is to assess pain
reduction via radiofrequency (RF) ablation. The Company’s
catheter-based microchip sensing array used to detect and
differentiate neural signaling was not used in this trial and will
be evaluated in future studies.
The first five patients were enrolled and
treated according to protocol in the beginning of the trial to
familiarize the Principal Investigator (“PI”) with the procedure
and will not be included in the analysis of the trial objectives.
These first five “lead-in” patients successfully completed the
procedure per protocol with no immediate procedural-related
complications or significant adverse events. The Company has
reported positive preliminary results at 7-Day post procedure and
for the 4-6 week follow-up.
The primary objective of the Trial is to assess
the success rate of ablating relevant nerves to mitigate pain in
patients with pancreatic cancer pain utilizing RF ablation in a
transvascular approach to the nerves in the region. Secondary
objectives include assessing the incidence of device- and
procedure-related adverse events up to 4-6 weeks post-procedure;
estimating the change in pain levels from pre- to post-procedure;
and estimating the change in quality of life from pre- to
post-procedure. All patients who have had a successful procedure
will be evaluated at 7 days, 4–6 weeks and at 3 months
post-procedure. All patients entered the study with severe
abdominal pain from unresectable pancreatic cancer and a life
expectancy of 3 months or less. Following the successful completion
of the procedure, two patients have since succumbed to their
disease. Both events were expected outcomes and not related to the
trial procedure.
As previously announced, Autonomix has amended
the Trial protocol to include the gathering of additional
information on tumor encroachment on the vessels, as well as other
key bio-measurements that may correlate with effective nerve
ablation. Additionally, the Company has further defined severe pain
for inclusion criteria as a 7 or above on the VAS scale as
indicated by the patient rather than physician determination. A
total of twenty (20) additional patients will be enrolled in the
Trial that will be formally included in the Trial data results and
analysis of Trial objectives. Suitability is determined by the
primary oncologist caring for the patients with the treating PI
confirming eligibility for the Trial. Autonomix commenced patient
screening under the amended protocol in May 2024 and remains on
track to complete enrollment in the Trial by year-end.
About Autonomix Medical,
Inc.
Autonomix is a medical device company focused on
advancing innovative technologies to revolutionize how diseases
involving the nervous system are diagnosed and treated. The
Company’s first-in-class platform system technology includes a
catheter-based microchip sensing array that may have the ability to
detect and differentiate neural signals with approximately 3,000
times greater sensitivity than currently available technologies. We
believe this will enable, for the first time ever, transvascular
diagnosis and treatment of diseases involving the peripheral
nervous system virtually anywhere in the body.
We are initially developing this technology for
the treatment of pain, with initial trials focused on pancreatic
cancer, a condition that causes debilitating pain and is without a
reliable solution. Our technology constitutes a platform to address
dozens of indications, including cardiology, hypertension and
chronic pain management, across a wide disease spectrum. Our
technology is investigational and has not yet been cleared for
marketing in the United States.
For more information, visit autonomix.com and
connect with the Company on X, LinkedIn, Instagram and
Facebook.
Forward Looking Statements
Some of the statements in this release are
“forward-looking statements,” which involve risks and
uncertainties. Forward-looking statements in this press release
include, without limitation, the potential of the technology to
treat pain associated with pancreatic cancer, to successfully
enroll patients within the specific timeframe, and to complete its
clinical study in pancreatic cancer pain. Such forward-looking
statements can be identified by the use of words such as “should,”
“might,” “may,” “intends,” “anticipates,” “believes,” “estimates,”
“projects,” “forecasts,” “expects,” “plans,” and
“proposes.”Although Autonomix believes that the expectations
reflected in these forward-looking statements are based on
reasonable assumptions, there are a number of risks and
uncertainties that could cause actual results to differ materially
from such forward-looking statements. You are urged to carefully
review and consider any cautionary statements and other
disclosures, including the statements made under the heading “Risk
Factors” and elsewhere in the Annual Report on Form 10-K filed with
the U.S. Securities and Exchange Commission (SEC) on May 31, 2024.
Forward-looking statements speak only as of the date of the
document in which they are contained and Autonomix does not
undertake any duty to update any forward-looking statements except
as may be required by law.
Investor and Media Contact
JTC Team, LLCJenene
Thomas908-824-0775autonomix@jtcir.com
1 https://pmc.ncbi.nlm.nih.gov/articles/PMC9160802/ 2
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9160802/pdf/CAM4-11-2296.pdf
3https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8176967/#:~:text=Conversely%2C%20patients%20with%20less%20pain,complementary%20and%20alternative%20medicine%20therapies
4 Michalski CW, Oti FE, Erkan M et al. Cannabinoids in pancreatic
cancer: Correlation with survival and pain. Int J Cancer
2008;122:742–750.5 Muller MW, Friess H, Koninger J et al. Factors
influencing survival after bypass procedures in patients with
advanced pancreatic adenocarcinomas. Am J Surg 2008;195:221–228.6
Scarborough BM, Smith CB. Optimal pain management for patients with
cancer in the modern era. CA Cancer J Clin 2018;68:182–196.7
D'Haese JG, Hartel M, Demir IE et al. Pain sensation in pancreatic
diseases is not uniform: The different facets of pancreatic pain.
World J Gastroenterol 2014;20:9154–9161.8 Staats PS, Hekmat H,
Sauter P et al. The effects of alcohol celiac plexus block, pain,
and mood on longevity in patients with unresectable pancreatic
cancer: A double‐blind, randomized, placebo‐controlled study. Pain
Med 2001;2:28–34.9 Hameed M, Hameed H, Erdek M. Pain management in
pancreatic cancer. Cancers (Basel) 2010;3:43–60.
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