ProMIS Neurosciences Inc. (Nasdaq: PMN), a clinical-stage
biotechnology company focused on the generation and development of
antibody therapeutics targeting toxic misfolded proteins in
neurodegenerative diseases such as Alzheimer’s disease (AD),
amyotrophic lateral sclerosis (ALS) and multiple system atrophy
(MSA), today announced financial results for the fiscal year ended
December 31, 2023 and provided a corporate update.
“I am pleased to have taken the helm of ProMIS at the beginning
of 2024 and am proud of the meaningful progress the team has made
to date as ProMIS made the transition to a clinical development
company. Importantly, we are nearing the initial read out from our
first-in-human studies of our lead product candidate, PMN310, as a
potential treatment for AD,” stated Neil Warma, Interim Chief
Executive Officer of ProMIS Neurosciences.
“As previously noted, we are nearing completion of the Phase 1a
single ascending dose (SAD) clinical trial of PMN310 in AD and
remain on track to report top-line data midyear, which will include
safety data and PMN310 exposure levels in blood and cerebrospinal
fluid (CSF). Moving forward, our goal is to advance PMN310 into a
Phase 1b multiple ascending dose (MAD) study in AD patients, which
could provide the first proof-of-concept data demonstrating that
PMN310 has the potential to positively benefit patients with AD.
This is a very exciting opportunity for both ProMIS and the AD
patients we aim to serve. In addition, it may have the potential to
lead the way for us to advance our differentiated platform in other
neurodegenerative diseases, such as ALS, MSA and Parkinson’s
disease,” stated Mr. Warma.
“We are diligently identifying ways to explore the potential
application of our differentiated platform while not distracting
our focus from our lead development program, PMN310, and our tight
control on cash management. Specific to our pipeline candidates, we
have and will continue to publish and present key data as each
progresses and remain excited about the early data generated across
a number of neurodegenerative diseases. We look forward to the
ongoing development of our novel antibody therapies and to
achieving a number of potentially value-creating milestones
throughout the balance of the year.”
Recent Highlights
Alzheimer’s Disease Program (PMN310)
PMN310, ProMIS’ lead compound, is a humanized IgG1 antibody
directed against toxic amyloid beta oligomers (AβO) that are
believed to be a major driver of AD.
- ProMIS dosed the
first participants in a first-in-human Phase 1a clinical trial of
PMN310 as a potential treatment for AD in November 2023 (Study
NCT06105528). The Phase 1a clinical trial is a double-blind,
placebo-controlled, single ascending dose study of the safety,
tolerability, and pharmacokinetics of PMN310 infusions in up to
five cohorts of eight healthy volunteers. PMN310 exposure levels in
blood and cerebrospinal fluid (CSF) will be evaluated as well as
safety.
- The Company
expects to report top-line data from the Phase 1a portion of the
study in mid-2024, which will include safety data and exposure
levels of antibodies in blood and CSF.
Discovery Programs
ProMIS continues to advance its amyloid beta vaccine program in
AD based on its oligomer target epitope(s).
- In January 2024, ProMIS announced
the selection of a lead vaccine candidate, PMN400, against multiple
synucleinopathies including MSA, Parkinson’s disease and Lewy Body
Dementia.
- Using a proprietary computational
platform, ProMIS identified potential conformational epitopes
(misfolded portions) unique to toxic alpha-synuclein involved in
synucleinopathies. Formulations of several of these epitopes were
tested in mouse vaccination studies leading to PMN400’s selection
as a lead vaccine candidate for testing in mouse models replicating
cognitive and motor deficits of human disease.
- In December 2023, ProMIS reported
data identifying Receptor for Activated C-Kinase 1 (RACK1) as a
novel misfolded protein target for the potential treatment of ALS
and frontotemporal lobar degeneration (FTLD), which data were
published in Acta Neuropathologica Communications.
Corporate
- In January 2024, the Company
announced the appointment of Neil Warma as the interim Chief
Executive Officer. Mr. Warma is a seasoned biotechnology executive
with more than 25 years of leadership experience. Mr. Warma has
served on the Company’s Board of Directors for the past two years
and remains as a director.
- In March 2024, ProMIS added key
U.S. and international patent allowances to further protect the
Company’s monoclonal antibody therapeutic for the treatment of
AD.
Full Year 2023 Financial Highlights
- Cash and cash equivalents were $12.6
million as of December 31, 2023, compared to $5.9 million as of
December 31, 2022. During the third quarter of 2023, the Company
raised $20.4 million in gross proceeds from a private investment in
public equity financing, less $2.7 million of issuance costs.
- Research and development expenses
were $7.9 million for the fiscal year ended December 31, 2023,
compared to $16.1 million for the same period in 2022. The decrease
was primarily attributable to a decrease in direct and external
research and development expenses as the Company focused on
advancing its lead program, PMN310, which entered the clinic in
November 2023.
- General and administrative expenses
modestly decreased to $6.4 million for the year ended December 31,
2023, compared to $7.3 million for the same period in 2022.
- Net loss was $13.2 million for the
full year ended December 31, 2023, compared to a net loss of $18.1
million for full year in 2022.
About ProMIS Neurosciences Inc.
ProMIS Neurosciences Inc. is a clinical-stage biotechnology
company focused on generating and developing antibody therapeutics
selectively targeting toxic misfolded proteins in neurodegenerative
diseases such as Alzheimer’s disease (AD), amyotrophic lateral
sclerosis (ALS) and multiple system atrophy (MSA). The Company’s
proprietary target discovery engine is based on the use of two
complementary techniques. The Company applies its thermodynamic,
computational discovery platform - ProMIS™ and Collective
Coordinates - to predict novel targets known as Disease Specific
Epitopes on the molecular surface of misfolded proteins. Using this
unique approach, the Company is developing novel antibody
therapeutics for AD, ALS and MSA. ProMIS has offices in Toronto,
Ontario and Cambridge, Massachusetts. To learn more, visit the
Company’s website at www.promisneurosciences.com.
Forward-looking Statements
Nasdaq has not reviewed and does not accept responsibility for
the adequacy or accuracy of this release. Certain information in
this news release constitutes forward-looking statements and
forward-looking information (collectively, “forward-looking
information”) within the meaning of applicable securities laws. In
some cases, but not necessarily in all cases, forward-looking
information can be identified by the use of forward-looking
terminology such as “plans”, “targets”, “expects” or “does not
expect”, “is expected”, “excited about”, “an opportunity exists”,
“is positioned”, “estimates”, “intends”, “assumes”, “anticipates”
or “does not anticipate” or “believes”, or variations of such words
and phrases or state that certain actions, events or results
“may”, “could”, “would”, “might”, “will” or “will be taken”,
“occur” or “be achieved”. In addition, any statements that refer
to expectations, projections or other characterizations of future
events or circumstances contain forward-looking information.
Specifically, this news release contains forward-looking
information relating to targeting of toxic misfolded proteins in
neurodegenerative diseases that the Company believes may directly
address fundamental AD pathology (including the belief and
understanding that toxic oligomers of amyloid-beta are a major
driver of AD) and have greater therapeutic potential due to
reduction of off-target activity, the progress of the Company’s
Phase 1a study, plans to advance PMN310 into a Phase 1b MAD study
in AD patients, the potential for such studies to provide the first
proof-of-concept data for PMN310, the potential that PMN310 has the
potential to positively benefit patients with AD, statements
related to the presentation of data, including the timing thereof,
and the significance of such data, information on the Company’s
beliefs regarding the significance of preclinical data, the
Company’s pipeline, including application of its platform to other
diseases, statements regarding a computationally-derived
amyloid-beta (Aβ) vaccine for AD and the Company’s PMN310 antibody
and vaccine candidate, management’s belief that its patented
platform technology has created an antibody candidate specific to
toxic misfolded oligomers known to be present in Alzheimer’s
disease, the anticipated use of proceeds from the private
placement, the progression of earlier stage antibody candidates for
multiple synucleinopathies including MSA, Parkinson’s disease and
Lewy Body Dementia (PMN400), the ability to continue its growth and
realize the anticipated contribution of the members of its board of
directors and executives to its operation and progress, the ability
to optimize the impact of its collaborations on its development
programs, statements regarding the timing of regulatory filings
regarding its development programs, use of capital expenses, future
accumulated deficit and other financial results in the future,
ability to fund operations, the ability to maintain enough
liquidity to execute its business plan and its ability to continue
as a going concern. Statements containing forward-looking
information are not historical facts but instead represent
management's current expectations, estimates and projections
regarding the future of our business, future plans, strategies,
projections, anticipated events and trends, the economy and other
future conditions. Forward-looking information is necessarily based
on a number of opinions, assumptions and estimates that, while
considered reasonable by the Company as of the date of this news
release, are subject to known and unknown risks, uncertainties and
assumptions and other factors that may cause the actual results,
level of activity, performance or achievements to be materially
different from those expressed or implied by such forward-looking
information, including, but not limited to, the Company’s ability
to fund its operations and continue as a going concern, its
accumulated deficit and the expectation for continued losses and
future financial results. Important factors that could cause actual
results to differ materially from those indicated in the
forward-looking information include, among others, the factors
discussed throughout the “Risk Factors” section of the Company's
most recently filed Annual Report on Form 10-K for the year ended
December 31, 2023 and in its subsequent filings filed with the
United States Securities and Exchange Commission. Except as
required by applicable securities laws, the Company undertakes no
obligation to publicly update any forward-looking information,
whether written or oral, that may be made from time to time,
whether as a result of new information, future developments or
otherwise.
For Investor Relations, please contact:Stern
Investor RelationsAnne Marie Fields, Managing
Directorannemarie.fields@sternir.com
--Tables to Follow--PROMIS
NEUROSCIENCES INC.Consolidated Balance
Sheets(expressed in US dollars, except share
amounts)(unaudited)
|
|
|
|
|
|
|
|
|
December 31, |
|
|
2023 |
|
|
2022 |
|
Assets |
|
|
|
|
|
|
Current assets: |
|
|
|
|
|
|
Cash |
|
$ |
12,598,146 |
|
|
$ |
5,875,796 |
|
Short-term investments |
|
|
32,358 |
|
|
|
31,009 |
|
Prepaid expenses and other current assets |
|
|
988,641 |
|
|
|
996,682 |
|
Total current assets |
|
|
13,619,145 |
|
|
|
6,903,487 |
|
Property and equipment,
net |
|
|
— |
|
|
|
321 |
|
Intangible assets, net |
|
|
— |
|
|
|
20,838 |
|
Total assets |
|
$ |
13,619,145 |
|
|
$ |
6,924,646 |
|
Liabilities and
Shareholders' Equity (Deficit) |
|
|
|
|
|
|
Current liabilities: |
|
|
|
|
|
|
Accounts payable |
|
$ |
7,843,136 |
|
|
$ |
2,975,398 |
|
Accrued liabilities |
|
|
1,506,526 |
|
|
|
3,437,646 |
|
Total current liabilities |
|
|
9,349,662 |
|
|
|
6,413,044 |
|
Share-based compensation
liability |
|
|
422,002 |
|
|
|
— |
|
Warrant liability |
|
|
94,185 |
|
|
|
1,859,374 |
|
Total liabilities |
|
|
9,865,849 |
|
|
|
8,272,418 |
|
Commitments and
contingencies |
|
|
|
|
|
|
Shareholders' equity
(deficit): |
|
|
|
|
|
|
Series 1 Convertible Preferred Shares, no par value, 70,000,000
shares authorized, 0 and 70,000,000 shares issued and outstanding
as of December 31, 2023 and December 31, 2022,
respectively |
|
|
— |
|
|
|
— |
|
Series 2 Convertible Preferred Shares, no par value, unlimited
shares authorized, 1,166,667 and 0 shares issued and outstanding as
of December 31, 2023 and December 31, 2022,
respectively |
|
|
— |
|
|
|
— |
|
Common shares, no par value, unlimited shares authorized,
18,885,254 and 8,579,284 shares issued and outstanding as of
December 31, 2023 and December 31, 2022,
respectively |
|
|
— |
|
|
|
— |
|
Additional paid-in capital |
|
|
97,590,426 |
|
|
|
79,101,061 |
|
Accumulated other comprehensive loss |
|
|
(371,184 |
) |
|
|
(195,369 |
) |
Accumulated deficit |
|
|
(93,465,946 |
) |
|
|
(80,253,464 |
) |
Total shareholders' equity
(deficit) |
|
|
3,753,296 |
|
|
|
(1,347,772 |
) |
Total liabilities and
shareholders' equity (deficit) |
|
$ |
13,619,145 |
|
|
$ |
6,924,646 |
|
PROMIS
NEUROSCIENCES INC.Consolidated Statements of
Operations and Comprehensive Loss(expressed in US
dollars, except share
amounts)(unaudited)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Years Ended December 31, |
|
|
2023 |
|
|
2022 |
|
Operating expenses: |
|
|
|
|
|
|
Research and development |
|
$ |
7,883,165 |
|
|
$ |
16,087,168 |
|
General and administrative |
|
|
6,379,568 |
|
|
|
7,292,744 |
|
Total operating expenses |
|
|
14,262,733 |
|
|
|
23,379,912 |
|
Loss from operations |
|
|
(14,262,733 |
) |
|
|
(23,379,912 |
) |
|
|
|
|
|
|
|
Other income (expense): |
|
|
|
|
|
|
Change in fair value of financial instruments |
|
|
866,738 |
|
|
|
4,176,767 |
|
Other interest expense |
|
|
(201,390 |
) |
|
|
— |
|
Interest expense on convertible debt |
|
|
— |
|
|
|
(282,064 |
) |
Gain on extinguishment of convertible debt and derivative
liability |
|
|
— |
|
|
|
1,307,421 |
|
Other income |
|
|
384,903 |
|
|
|
115,525 |
|
Total other income (expense), net |
|
|
1,050,251 |
|
|
|
5,317,649 |
|
|
|
|
|
|
|
|
Net loss |
|
|
(13,212,482 |
) |
|
|
(18,062,263 |
) |
Other comprehensive loss |
|
|
|
|
|
|
Foreign currency translation adjustment |
|
|
— |
|
|
|
(7,450 |
) |
Comprehensive loss |
|
$ |
(13,212,482 |
) |
|
$ |
(18,069,713 |
) |
|
|
|
|
|
|
|
Net loss per share, basic and
diluted |
|
$ |
(1.07 |
) |
|
$ |
(2.41 |
) |
|
|
|
|
|
|
|
Weighted-average shares
outstanding of common shares, basic and diluted |
|
|
12,292,707 |
|
|
|
7,502,609 |
|
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