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NeuroSense Announces Second Quarter 2023 Financial Results and Provides Business Update

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Rhea-AI Summary
NeuroSense Therapeutics completed patient enrollment for its Phase 2b ALS study and expects topline results in Q4 2023. The company raised $4.5 million in capital, providing funding until Q2 2024. NeuroSense also announced a strategic scientific agreement with Biogen and is preparing for a Phase 2 AD trial and exploring co-development for PD indication.
Positive
  • NeuroSense completed patient enrollment for its Phase 2b ALS study, with topline results expected in Q4 2023.
  • The company raised $4.5 million in capital, extending its cash runway until Q2 2024.
  • NeuroSense announced a strategic scientific agreement with Biogen to evaluate the impact of PrimeC on neurofilament levels in ALS patients.
  • The company is preparing for a Phase 2 AD trial and published data from a biomarker study in Parkinson's disease.
Negative
  • None.
  • ALS Phase 2b PARADIGM Trial Completed Patient Enrollment
  • Topline results expected in Q-4 2023
  • Cash runway beyond topline clinical study readouts, into Q-2 2024

CAMBRIDGE, Mass., Aug. 16, 2023 /PRNewswire/ -- NeuroSense Therapeutics Ltd. (NASDAQ: NRSN) ("NeuroSense"), a company developing treatments for severe neurodegenerative diseases, today published its financial results for the quarter ended June 30, 2023 and provided a business update.

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"Throughout this quarter NeuroSense achieved multiple milestones, including the completion of patient enrollment of our Phase 2b ALS study. Results observed from several biomarker studies are promising, especially in that they support our clinical strategy. The findings, along with the data we collect from our Phase 2b study, could inform the optimization of a pivotal Phase 3 study of PrimeC in ALS," stated NeuroSense's CEO, Alon Ben-Noon. "We are well positioned to complete our Phase 2b study and report topline results in Q-4 2023."

Business Update

Capital Raise of $4.5 Million

In Q-2 2023, NeuroSense raised $4.5 million in capital and based on our current expense projections is now funded into Q-2 2024, well beyond the expected timing for the release of topline results from the PARADIGM study.

Phase 2b Amyotrophic Lateral Sclerosis (ALS) PARADIGM Trial Completed Patient Enrollment

In Q-2 2023, NeuroSense completed enrollment of its double-blind, placebo-controlled, multi-center Phase 2b clinical trial using a unique upgraded formulation of PrimeC, which is designed to maximize the synergistic effect between the compounds in its combination drug. The clinical trial endpoints include assessment of ALS biomarkers, evaluation of clinical efficacy, and improvement in quality of life to demonstrate an attenuation in disease progression. Elucidation of the mechanism of action of PrimeC utilizing data from the upcoming Phase 2b trial may enable patient stratification and increase the likelihood of success in a pivotal trial. Topline results are expected in Q-4 2023. Significantly, over 96% of participants who completed the trial chose to continue in the study and be treated with PrimeC through a 12-month open-label extension.

Strategic Scientific Agreement with Biogen

In May 2023, NeuroSense announced a collaboration agreement with Biogen to evaluate the impact of PrimeC on neurofilament levels in the plasma of participants in NeuroSense's Phase 2b ALS PARADIGM trial. Biogen will fund this meaningful neurofilament biomarker study and upon receipt of results has the right of first refusal to co-develop and/or commercialize PrimeC for the treatment of ALS for a limited time.

Phase 2 Alzheimer's Disease (AD) Trial Under Preparation

In Q-1 2023, NeuroSense published data from a biomarker study, which revealed elevated levels of novel biomarker TDP-43 in AD as compared to healthy controls. NeuroSense believes these results support the therapeutic potential of its combination drug platform for AD. NeuroSense is preparing to commence a Phase 2 double-blind proof-of-concept clinical study, with regulatory submissions and site readiness ongoing during Q-2 2023 and first patient enrolled expected in the next few weeks.

Parkinson's Disease (PD) Biomarker Study Completed

In Q-2 2023, NeuroSense published data from a biomarker study in Parkinson's disease, which observed a statistically significant decrease in levels of AGO2, a novel PD biomarker, in newly diagnosed PD patients when compared to the healthy control group. The Company is exploring potential co-development for the PD indication.

Key Industry Conferences

In addition, NeuroSense joined EverythingALS in the EverythingALS Digital Biomarkers Summit in July 2023.

Financial Summary 

Six Months Ended June 30, 2023

  • Research and development expenses for the six months ended June 30, 2023 increased to $4.0 million compared to $3.17 million for the six months ended June 30, 2022. This increase was primarily attributable to subcontractors and consultants with respect to our Phase 2b clinical study that started in May 2022. NeuroSense expects research and development expenses to remain steady until the end of 2023, and then slightly decrease as a result of completing the double blind stage of the clinical study.  
  • General and administrative expenses for the six months ended June 30, 2023 decreased to $3.11 million compared to $3.69 million for the six months ended June 30, 2022. This decrease was primarily attributable to lower share-based compensation and insurance expenses. NeuroSense expects that general and administrative expenses will remain at the same level through 2023.
  • Financing expenses for the six months ended June 30, 2023 and 2022, were $2.2 million and $58,000, respectively. The increase of $2.14 million, or 3,686%, was mainly attributed to liability with respect to warrants and prefunded warrants.
  • Financing income for the six months ended June 30, 2023 and 2022 were $200,000 and $716,000, respectively. The decrease of $516,000, or 72%, was mainly attributed to change in rate differentials and warrants.
  • Operating expenses for the six months ended June 30, 2023 were $7.12 million compared to $6.85 million for the six months ended June 30, 2022 due to the reasons described above.

As of June 30, 2023, NeuroSense had cash and short-term deposits of $7.1 million. NeuroSense reported a $1.55 million deficit in shareholder equity as of June 30, 2023, resulting from the required accounting treatment under IFRS related to the pre-funded warrants and warrants that the Company issued as part of the $4.5 million financing completed on June 26, 2023. A summary of the Company's unaudited financial results is included in the tables below.

Condensed Interim Unaudited Statements of Financial Position
U.S. dollars in thousands


June 30,
2023

December 31,
2022

Assets






Current assets:



Cash

7,089

3,543

Short term deposits

-

3,547

Other receivables

434

255

Restricted deposit

38

36

Total current assets

7,561

7,381




Non-current assets:



Property, plant and equipment, net

93

77

Right of use assets

191

229

Non-current restricted deposit

23

23

Total non-current assets

307

329




Total assets

7,868

7,710




Liabilities and Equity






Current liabilities:



Trade payables

1,090

498

Other payables

1,915

1,228

Total current liabilities

3,005

1,726




Non Current liabilities:



Long term lease liability

104

147

Liability in respect of warrants and pre-funded warrants                                         

6,304

218


6,408

365




Total liabilities

9,413

2,091




Shareholders' equity: 



Ordinary shares

-

-

Share premium and capital reserve                                                                         

28,355

26,405

Accumulated deficit

(29,900)

(20,786)

Total Shareholders' equity (deficit)

(1,545)

5,619




Total liabilities and shareholders' equity (deficit)

7,868

7,710

 

 

Condensed Interim Unaudited Statements of Income and Comprehensive Loss
U.S. dollars in thousands except share and per share data


Six months

ended 
June 30,

2023

Six months

ended 

June 30, 

2022

For the year

ended 

December 31, 

2022








Research and development expenses

(4,005)

(3,166)

(6,416)





General and administrative expenses

(3,113)

(3,688)

(7,136)





Operating loss

(7,118)

(6,854)

(13,552)





Financing expenses

(2,196)

(58)

(45)





Financing income

200

716

1,257





Financing income (expenses), net

(1,996)

658

1,212





Net loss and comprehensive loss

(9,114)

(6,196)

(12,340)

Basic and diluted net loss per share

(0.77)

(0.55)

(1.07)









Weighted average number of shares

outstanding used in 

computing basic and diluted net loss

per share

 

13,623,042

11,294,701

11,504,521

 

 

Condensed Interim Unaudited Statements of Changes in Equity
U.S. dollars in thousands



 

 

 

Ordinary

Shares

 

 

Share
Premium
And

Capital 

Reserve

 

 

 

Accumulated

Deficit

 

 

 

Total Equity

(Deficit)

Six months ended June 30, 2023:












Balance as at January 1, 2023


-

26,405

(20,786)

5,619

Share-based compensation


-

1,945

-

1,945

Exercise of options


-

5

-

5

Net loss and comprehensive loss


-

-

(9,114)

(9,114)







Balance as at June 30, 2023


-

28,355

(29,900)

(1,545)







Six months ended June 30, 2022:












Balance as at January 1, 2022


-

17,452

(8,446)

9,006

Share-based compensation


-

2,808

-

2,808

Net loss and comprehensive loss


-

-

(6,196)

(6,196)

Cancelation of options



(96)

-

(96)

Exercise of warrants


-

4,314

-

4,314







Balance as at June 30, 2022


-

24,478

(14,642)

9,836







For the year ended December 31, 2022:












Balance as at January 1, 2022


-

17,452

(8,446)

9,006







Share-based compensation


-

4,735

-

4,735

Net loss and comprehensive loss


-

-

(12,340)

(12,340)

Cancelation of options


-

(96)

-

(96)

Exercise of warrants


-

4,314

-

4,314







Balance as at December 31, 2022


-

26,405

(20,786)

5,619

 

 

Condensed Interim Unaudited Statements of Cash Flows 
U.S. dollars in thousands


Six months

ended

June 30,

2023

Six months

ended

June 30,

2022

For the year

ended

December 31,

2022





Cash flows from operating activities




Net loss for the period

(9,114)

(6,196)

(12,340)





Adjustments:








Depreciation and Amortization

47

41

89

Share-based compensation

1,784

2,808

5,105

Revaluation of liability in respect to warrants and pre-

funded warrants

 

(73)

 

(693)

(1,166)

Loss from financial instruments issuance as of the date of

issuance

1,659







Finance expenses (income), net

365

65

(24)





Changes in assets and liabilities:




Decrease (increase) in other receivables

(179)

(397)

55

Increase in trade payables

592

81

459

Increase in other payables

841

5

236





Net cash used in operating activities

(4,078)

(4,286)

(7,586)





Cash flows from investing activities




Interest received

47

-

49

Change in short term deposit

3,500

(6,000)

(3,500)

Investment in restricted deposit

(2)

(19)

(20)

Purchase of property, plant and equipment

(25)

(30)

(70)

Net cash provided by (used in) investing activities

3,520

(6,049)

(3,541)





Cash flows from financing activities




Payment in respect of cancellation of options

-

(96)

(96)

Exercise of warrants and options

5

3,870

3,870

Issuance of shares, warrants and pre-funded warrants, net

4,142

-

-

Repayment of lease liability

(44)

(67)

(79)

Net cash provided by financing activities

4,103

3,707

3,695





Effects of exchange rate changes on cash and cash equivalents

1

(86)

(88)





Net increase (decrease) in cash and cash equivalents

3,546

(6,714)

(7,520)





Cash and cash equivalents at beginning of the period

3,543

11,063

11,063





Cash and cash equivalents at end of the period

7,089

4,349

3,543

About NeuroSense
NeuroSense Therapeutics, Ltd. is a clinical-stage biotechnology company focused on discovering and developing treatments for patients suffering from debilitating neurodegenerative diseases. NeuroSense believes that these diseases, which include amyotrophic lateral sclerosis (ALS), Alzheimer's disease and Parkinson's disease, among others, represent one of the most significant unmet medical needs of our time, with limited effective therapeutic options available for patients to date. Due to the complexity of neurodegenerative diseases and based on strong scientific research on a large panel of related biomarkers, NeuroSense's strategy is to develop combined therapies targeting multiple pathways associated with these diseases.

For additional information, we invite you to visit our website and follow us on LinkedIn and Twitter.

Forward-Looking Statements

This press release contains "forward-looking statements" that are subject to substantial risks and uncertainties. All statements, other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use of words such as "anticipate," "believe," "contemplate," "could," "estimate," "expect," "intend," "seek," "may," "might," "plan," "potential," "predict," "project," "target," "aim," "should," "will" "would," or the negative of these words or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements are based on NeuroSense Therapeutics' current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict and include statements regarding the timing of top-line results of, and the results of, the PARADIGM clinical trial, cash runway estimate and the timing of patient enrollment in our Alzheimer's Disease (AD) clinical trial.    Further, forward-looking statements are subject to a number of risks and uncertainties as a result of which actual results could differ materially and adversely from those anticipated or implied in the forward looking statements. These risks include a delay in the reporting of top-line results from PARADIGM clinical trial and a delay in patient enrollment in our AZ clinical trial; greater than anticipated costs and expenses; the potential for PrimeC to safely and effectively target ALS; preclinical and clinical data for PrimeC; the timing of current and future clinical trials, timing for reporting data; the nature, strategy and focus of the company and further updates with respect thereto; the development and commercial potential of any product candidates of the company; and other risks and uncertainties set forth in NeuroSense's filings with the Securities and Exchange Commission (SEC), including NeuroSense's Annual Report on Form 20-F filed with the SEC on March 22, 2023. Forward-looking statements contained in this announcement are made as of this date, and NeuroSense Therapeutics Ltd. undertakes no duty to update such information except as required under applicable law.

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SOURCE NeuroSense

FAQ

What is the latest update from NeuroSense Therapeutics?

NeuroSense completed patient enrollment for its Phase 2b ALS study and expects to release topline results in Q4 2023.

How much capital did NeuroSense raise?

NeuroSense raised $4.5 million in capital.

What is the strategic scientific agreement announced by NeuroSense?

NeuroSense announced a collaboration agreement with Biogen to evaluate the impact of PrimeC on neurofilament levels in ALS patients.

What clinical trials is NeuroSense preparing for?

NeuroSense is preparing for a Phase 2 AD trial and exploring potential co-development for the PD indication.

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