Spectral Medical Announces Third Quarter Results and Provides Corporate Update

Spectral Medical Announces Third Quarter Results and Provides Corporate Update




Spectral Medical Announces Third Quarter Results and Provides Corporate Update

Tigris Trial Enrollment at 135 Patients
Strengthened Balance Sheet with Expected Funds to Complete Tigris Trial Enrollment

TORONTO, Nov. 08, 2024 (GLOBE NEWSWIRE) — Spectral Medical Inc. (“Spectral” or the “Company”) (TSX: EDT), a late-stage theranostic company advancing therapeutic options for sepsis and septic shock, today announced its financial results for the third quarter ended September 30, 2024, and provided a corporate update.

Spectral has continued its significant progress throughout the third quarter of 2024 both clinically and operationally and year-to-date enrolled 54 patients for a total of 135 patients out of the 150 total patients target. The Company is focused on the final push to fully enroll and finish the Tigris trial, bringing the Company closer to FDA submission and potential FDA approval. In parallel to its clinical trial, the Company continues to work closely with its commercialization partner, Baxter.

Dr. John Kellum, Chief Medical Officer of Spectral Medical, stated, “We continue to witness robust enrollment activity in 2024, with record enrollment rates over several months of the year. Screening rates have been at approximately 50% higher throughout the year compared to 2023. Tigris is approaching the final phase of the trial, and we have very dedicated investigators who believe in the project. In October, we experienced some disruptions due to Hurricane Helene – mainly the national saline shortage (required to prepare the device for treatment). Our clinical team is focused on trial site support and is working to help resolve this issue. We are committed alongside our trial sites to advancing Tigris and believe PMX, if ultimately approved, will play a major role in reducing the tragic rates of mortality caused by sepsis.”

“I am pleased with the increased level of activity across the Company and the resultant ramp up of patient enrollment throughout 2024. With the recent medical supply chain events negatively impacting enrollment, we anticipate a slight shift in finalizing Tigris enrollment into the early 2025 timeframe,” said Chris Seto, Chief Executive Officer of Spectral. “That being said, with the receipt of gross proceeds of approximately $11 million since the beginning of April, we believe we have secured funding to finalize Tigris enrollment.”

Corporate Highlights During & Subsequent to Third Quarter 2024

Tigris Trial and Regulatory Program

  • Patient Enrollment
    Total of 135 patients randomized to date out of the target 150 total patients to be enrolled in the Tigris trial.
    • Year-to-date enrollment experienced in 2024 has been robust with 54 patients enrolled so far.
    • Record monthly enrollment to start Q3 2024, with nine patients enrolled in July; followed by anticipated slowdown in August and September with lighter enrollment activity due to site vacation schedules.
    • Experienced significantly lower patient enrollment in October due to the impact of Hurricane Helene on the medical supply chain. The disruption in production of critical intravenous fluids has led to a rationing of saline, which is required to prepare PMX for treatment, negatively impacted patient enrollment, despite record patient screening levels. Our clinical team is working to help sites resolve this issue.
    • For more information on Hurricane Helene’s impact on the supply of critical intravenous fluids, see the following link: Letter to Health Care Leaders and Stakeholders on Impacts of Hurricane Helene from Secretary Becerra | HHS.gov
  • Tigris Sites
    Currently 22 Tigris sites participating.
    • Spectral clinical team focused on trial site management activities to ensure that Tigris sites have the support and resources to enroll patients as efficiently as possible.
  • Timing
    The Company continues to focus on finalizing the Tigris trial within the reasonably shortest timelines. Based on the current rate of enrollment, management believes Tigris should be completed in first quarter of 2025.

PMX Commercialization

  • Baxter Partnership Activities
    In anticipation of a positive Tigris trial outcome, the Company has been working closely with Baxter on post-approval marketing plans for PMX commercialization. This includes developing product branding, pricing and roll-out plans with numerous Baxter departments, including marketing, regulatory, clinical and reimbursement. Baxter has communicated its intention to undertake a broad marketing campaign on day one of FDA approval for PMX.
  • Prismax Sub-study
    The Company is also working with Baxter on a sub-study to obtain FDA clearance for hemoperfusion for Baxter’s Prismax device. The Prismax, with its leading installed base in ICUs throughout the U.S., is anticipated to be the primary ICU device utilized for PMX treatments on commercial launch.

Funding

  • Exercise of Anti-Dilution Pre-emptive Rights
    On July 19, 2024 the Company completed an additional non-brokered offering of US$1 million of 9% convertible notes of the Company (the “Notes”) at a price of US$1,000 per convertible note due on May 1, 2028 (the “Offering”). The Notes were sold to one of the Company’s largest shareholders pursuant to the exercise of their anti-dilution pre-emptive rights relating to the closing of the offering of the approximately CAD$8.5 million offering of Notes that was completed on May 30, 2024.
  • Share Warrant Exercise / Expired Warrants
    In the third quarter 232,500 share warrants were exercised for gross proceeds of approximately $114,250. These warrants were issued in conjunction with the Company’s July 27, 2021 and November 2, 2022 unit offerings.

    On July 29, 2024, 10,982,500 share warrants expired. These expired share warrants were issued in conjunction with the Company’s approximately $10 million unit offering which closed on July 27, 2021. As at the time of this MD&A, the Company has 7,730,464 share warrants outstanding.

  • Early conversion of Convertible notes issued on September 7, 2023
    On August 19, 2024, 150 Notes having a face value of USD $1,000 were converted into 509,850 Common Shares at a conversion rate of 3,399 Common Shares per USD$1,000 principal amount of the Notes.

    On September 25, 2024, 225 Notes having a face value of USD $1,000 were converted into 764,755 Common Shares at a conversion rate of 3,399 Common Shares per USD $ 1,000 principal amount of the Notes.

Change of Auditors

  • On July 11, 2024, the Company announced that MNP had been appointed as the auditors of the Company following the decision by PricewaterhouseCoopers LLP (“PWC”) to resign as the auditor of Spectral. The PWC resignation was not the result of any disagreement between the Company and PWC on any matter of accounting principles or practices, financial statement disclosure, or auditing scope or procedure.

Financial Review

Revenue for the three-months ended September 30, 2024 was $502,000 compared to $397,000 for the same three-month period last year, representing an increase of $105,000 or 26%. Revenue for nine months ended September 30, 2024, was $1,641,000 and $1,233,000 for the same period last year, representing an increase of $408,000 or 33%. Royalty revenue for the three-months ended September 30, 2024 was $NIL and $NIL for the same period prior year. Royalty revenue for the nine months ended September 30, 2024 was $135,000 compared to $126,000 for the same nine-month period last year. This is due to an increase in usage of the Company’s IP from one customer. Product Revenue for the three-months ended September 30, 2024 was $274,000 compared to $186,000 for the same three-month period last year, representing an increase of $88,000 or 47% Product revenue for nine months ended September 30, 2024 was $841,000 and $562,000, representing an increase of $279,000 or 50%.

Operating expenses for the three-months ended September 30, 2024, were $10,497,000, compared to $4,072,000 for the same period in the preceding year, an increase of $6,425,000 or 158%. The increase is majorly due to the change in Fair value adjustment for derivative liabilities which increased by $6,075,000 and also the Interest expense increased by $628,000 due to convertible notes payable issued on September 7, 2023, May 30, 2024 and July 19, 2024.

Operating expenses for the nine months ended September 30, 2024 were $20,194,000 compared to $10,292,000 for the same period in the preceding year, an increase of $9,902,000 or 96%. The change is primarily due to an increase in interest expense by $1,339,000 and Fair value adjustment in derivative liability increased by $6,530,000. All these increases are due to the funding received during September 2023, May 2024 and July 19, 2024. In addition, share-based compensation expense increased by $197,000. Lastly, consulting and professional fees increased by $352,000 due to increased site and patient fees related to the Tigris trial.

Clinical development and regulatory program costs (as disclosed in Note 13 of the condensed interim consolidated financial statements) were $638,000 for the three-months ended September 30, 2024 compared to $1,263,000 for the same period in the prior year. For the nine months ended September 30, 2024, clinical development costs are $3,015,000 compared to $3,258,000 for the corresponding period in the prior year. A significant portion of clinical trial and regulatory costs consists of consulting and professional fees paid to contract research organizations, clinical sites, and other clinical and regulatory consultants. The decrease in costs reflects decreased start up activity with respect to the initialization of new clinical sites and the absence of upfront CRO switching costs which were experienced in 2023.

Loss for the three-months ended September 30, 2024 was $9,995,000, $(0.04) per share compared to a loss of $3,804,000, $(0.01) per share for the same period in the prior year. The increased loss of $6,191,000 was due to increased operating expenses, partially offset by a reduction in loss from discontinued operations of $130,000 related to the reduction in Dialco operating expenses.

Loss for the nine months ended September 30, 2024 was $18,556,000, $(0.07) per share, compared to a loss of $9,184,000 $(0.03) per share, for the same period in the prior year. The increased loss of $9,372,000 was due to operating expenses, partially offset by a reduction in loss from discontinued operations of $122,000 related to the reduction in Dialco operating expenses.

The Company concluded the third quarter of 2024 with cash of $5,759,000 compared to $2,952,000 of cash on hand as of December 31, 2023.

The total number of common shares outstanding for the Company was 282,815,223 at September 30, 2024.

About Spectral 

Spectral is a Phase 3 company seeking U.S. FDA approval for its unique product for the treatment of patients with septic shock, Toraymyxin™ (“PMX”). PMX is a therapeutic hemoperfusion device that removes endotoxin, which can cause sepsis, from the bloodstream and is guided by the Company’s Endotoxin Activity Assay (EAA™), the only FDA cleared diagnostic for the risk of developing sepsis.

PMX is approved for therapeutic use in Japan and Europe and has been used safely and effectively on more than 340,000 patients to date. In March 2009, Spectral obtained the exclusive development and commercial rights in the U.S. for PMX, and in November 2010, signed an exclusive distribution agreement for this product in Canada. In July 2022, the U.S. FDA granted Breakthrough Device Designation for PMX for the treatment of endotoxic septic shock. Approximately 330,000 patients are diagnosed with septic shock in North America each year.

The Tigris Trial is a confirmatory study of PMX in addition to standard care vs standard care alone and is designed as a 2:1 randomized trial of 150 patients using Bayesian statistics. Endotoxic septic shock is a malignant form of sepsis https://www.youtube.com/watch?v=6RANrHHi9L8.

The trial methods are detailed in “Bayesian methods: a potential path forward for sepsis trials”.

Spectral is listed on the Toronto Stock Exchange under the symbol EDT. For more information, please visit www.spectraldx.com.

Forward-looking statement

Information in this news release that is not current or historical factual information may constitute forward-looking information within the meaning of securities laws. Implicit in this information, particularly in respect of the future outlook of Spectral and anticipated events or results, are assumptions based on beliefs of Spectral’s senior management as well as information currently available to it. While these assumptions were considered reasonable by Spectral at the time of preparation, they may prove to be incorrect. Readers are cautioned that actual results are subject to a number of risks and uncertainties, including the availability of funds and resources to pursue R&D projects, the successful and timely completion of clinical studies, the ability of Spectral to take advantage of business opportunities in the biomedical industry, the granting of necessary approvals by regulatory authorities as well as general economic, market and business conditions, and could differ materially from what is currently expected.

The TSX has not reviewed and does not accept responsibility for the adequacy or accuracy of this statement.

For further information, please contact:

Ali Mahdavi Chris Seto
Capital Markets & Investor Relations CEO
Spinnaker Capital Markets Inc. Spectral Medical Inc.
416-962-3300  
am@spinnakercmi.com cseto@spectraldx.com

Spectral Medical Inc.
Condensed Interim Consolidated Statements of Financial Position
In CAD (000s), except for share and per share data
(Unaudited)
           
  Notes September 30,
2024
December 31,
2023
(Refer Note 3)
January 1,
2023
(Refer Note 3)
 
  $ $ $  
Assets          
Current assets          
Cash   5,759 2,952 8,414  
Trade and other receivables   337 186 1,056  
Inventories   318 366 340  
Prepayments and other assets   882 621 276  
    7,296 4,125 10,086  
Non-current assets          
Right-of-use-asset   475 567 464  
Property and equipment   268 326 237  
Intangible asset   180 193 211  
Investment in Dialco   998  
Total assets   8,219 5,211 11,996  
Liabilities          
Current liabilities          
Trade and other payables   3,004 2,820 3,087  
Current portion of contract liabilities 7 502 727 696  
Current portion of lease liability   126 121 96  
Notes Payable 8&3 12,890 7,940 3,566  
Derivative Liability 8&4 17,405 6,310 2,674  
    33,927 17,918 10,119  
Non-current liability          
Lease liability   404 500 420  
Non-current portion of contract liabilities 7 5,170 3,342 4,011  
Total liabilities   39,501 21,760 14,550  
Shareholders’ (deficiency) equity 10        
Share capital   89,871 87,061 87,050  
Contributed surplus   10,148 8,916 8,773  
Share-based compensation   11,308 10,385 8,908  
Warrants   1,384 2,526 2,490  
Deficit   (143,993) (125,437) (109,775)  
Total shareholders’ (deficiency) equity   (31,282) (16,549) (2,554)  
Total liabilities and shareholders’ (deficiency) equity   8,219 5,211 11,996  

Spectral Medical Inc.
Condensed Interim Consolidated Statements of Loss and Comprehensive Loss
In CAD (000s), except for share and per share data
(Unaudited)
             
      Revised   Revised  
    (Refer Note 16)   (Refer Note 16)  
Notes Three months
ended Sep 30,
2024
Three months
ended Sep 30,
2023
Nine months
ended Sep 30,
2024
Nine months
ended Sep 30,
2023
 
    $ $ $  
Revenue 7&12  502 397 1,641 1,233  
Expenses            
Raw materials and consumables used   327 305 994 722  
Salaries and benefits 14 1,078 986 3,101 2,918  
Consulting and professional fees   1,282 1,198 3,652 3,300  
Regulatory and investor relations   284 110 585 414  
Travel and entertainment   136 63 407 245  
Facilities and communication   90 81 353 245  
Insurance   105 102 315 290  
Depreciation and amortization   64 57 191 172  
Interest expense 8 970 342 2,178 839  
Foreign exchange loss   (399) 46 129 (205)  
Share-based compensation   241 340 1,497 1,300  
Other expense   163 320 704 289  
Net loss on joint arrangement 6 41 205  
Fair value adjustment derivative liabilities 8 6,156 81 6,088 (442)  
    10,497 4,072 20,194 10,292  
Loss and comprehensive loss for the period from continuing operations   (9,995) (3,675) (18,553) (9,059)  
Gain (loss) from discontinued operations 5 (130) (3) (125)  
Loss and comprehensive loss for the period   (9,995) (3,805) (18,556) (9,184)  
Basic and diluted loss from continuing operations per common share 11 (0.04) (0.01) (0.07) (0.03)  
Basic and diluted loss from discontinued operations per common share 11 (0.00) (0.00) (0.00) (0.00)  
Basic and diluted loss per common share 11 (0.04) (0.01) (0.07) (0.03)  
Weighted average number of common shares outstanding – basic and diluted 11 281,705,359 278,604,718 280,269,516 278,569,902  

Spectral Medical Inc.
Condensed Interim Consolidated Statements of Changes in Shareholders’ Deficiency
In CAD (000s)
(Unaudited)
                     
  Notes Number of
Shares
Share
Capital
Contributed
surplus
  Share-based compensation Warrants Deficit   Total Shareholders’ (deficiency) equity
      $ $   $ $ $   $  
Balance January 1, 2023   278,547,804 87,050 8,773   8,908 2,490 (109,775)   (2,554)  
RSU released 10 28,457 11   (11)    
Warrants issued 10   179   179  
Warrants expired 10 143   (143)    
Loss and comprehensive loss for the period

    (9,184)   (9,184)  
Share-based compensation 10 –    1,300   1,300  
Revised (Refer note 16) Balance, September 30, 2023   278,576,261 87,061 8,916   10,197 2,526 (118,959)   (10,259)  
Loss and comprehensive loss for the period     (6,478)   (6,478)  
Share-based compensation 10   188   188  
Balance December 31, 2023   278,576,261 87,061 8,916   10,385 2,526 (125,437)   (16,549)  
Balance January 1, 2024   278,576,261 87,061 8,916   10,385 2,526 (125,437)   (16,549)  
Warrants exercised 10 982,500 618   (121)   497  
Warrants issued 10   211   211  
Warrants expired 10 1,232   (1,232)    
Share Options Exercised 10 1,867,627 1,163   (524)   639  
RSU released 10 114,210 50   (50)    
Notes Conversion 10 1,274,625 979     979  
Loss and comprehensive loss for the period     (18,556)   (18,556)  
Share-based compensation 10  –   1,497   1,497  
Balance September 30, 2024   282,815,223 89,871 10,148   11,308 1,384 (143,993)   (31,282)  

Spectral Medical Inc.
Condensed Interim Consolidated Statements of Cash Flows
In CAD (000s)
(Unaudited)
     
    Revised  
    (Refer note 16)  
  Nine months
ended
September 30,
2024
Nine months
ended
September 30,
2023
 
Cash flow provided by (used in)    
Operating activities    
Loss and comprehensive loss for the period (18,556) (9,184)  
Adjustments for:    
Depreciation on right-of-use asset 92 73  
Depreciation on property and equipment 85 87  
Amortization of intangible asset 13 19  
Amortization of deferred financing fee 788 373  
Unrealized foreign exchange gain/loss 76 (155)  
Interest expense on lease liability 25 30  
Accreted interest on notes payable 2,154 809  
Share-based compensation expense 1,497 1,300  
Net loss on joint venture arrangement 205  
Fair value adjustment derivative liabilities 6,088 (442)  
Changes in items of working capital:    
Trade and other receivables (151) 337  
Inventories 48 36  
Prepayments and other assets (261) (636)  
Trade and other payables (24) (781)  
Contract liabilities 1,603 (647)  
Net cash used in operating activities (6,523) (8,576)  
Investing activities    
Purchase of property and equipment (28) (15)  
Net cash used in investing activities (28) (15)  
Financing activities    
Financing charges paid (766) (641)  
Interest expense paid (794) (472)  
Lease liability payments (115) 110  
Proceeds from share options exercised 639  
Proceeds from share warrants exercised 497  
Proceeds from 9% convertible notes issued 9,897 6,212  
Net cash provided by financing activities 9,358 5,209  
Change in cash 2,807 (3,383)  
Cash, beginning of period 2,952 8,414  
Cash, end of period 5,759 5,031