Tigris Trial Enrollment Reaches 106 Patients
Bought Deal Financing Expected to Fund Completion of Tigris Trial Enrollment
Spectral has continued its significant progress throughout the first quarter of 2024 both clinically and operationally and year-to-date enrolled 25 patients for a total of 106 patients out of the 150 total patients target. The Company is focused on the final push to fully enroll and finish the Tigris trial and believes that the continued onboarding of new Tigris sites since the fourth quarter of 2023 could further accelerate enrollment and allow Spectral to rapidly reach the 150-patients target, 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,
Dr.
“I am pleased with the increased level of activity across the Company and its impact on establishing robust trial sites, thus resulting in a significant ramp up of patient enrollment. The recent pace of enrollment, combined with the quality and focus of the current and planned trial sites provide us with confidence in continued robust enrollment activity. The potential to sustain our current pace of enrollment could see us rapidly advance the trial towards completion in the late 2024 to early 2025 timeframe,” said
Corporate Highlights
Tigris:
- Total of 106 patients randomized to date out of the 150 total patients to be enrolled in the Tigris trial.
- accelerated enrollment experienced in 2024 to date, with 25 patients enrolled so far – represents the most robust enrollment rates since the start of the Tigris trial.
- Currently 22 Tigris sites onboarded
- addition of three new trial sites in the first quarter – the
University of Texas Health Sciences Center atHouston ,The Institute for Extracorporeal Life Support (San Antonio, TX ), andUCLA . - subsequent to the first quarter, the Company added one new site –
University of Virginia Health Sciences .
- addition of three new trial sites in the first quarter – the
- Investigator Meeting held March 12th and 13th
- The Company held a Tigris trial Investigator Meeting in conjunction with the 29th
International Conference on Advances in Critical Care Nephrology inSan Diego . - In-person meeting well-attended with multiple stakeholders present, including principal investigators and clinical research coordinators from existing and new trial sites, CRO, Beaufort, and representatives from the Spectral’s strategic partner
Baxter . - Focus of the meeting was on the practical aspects of diagnosing endotoxic septic shock and treating with PMX, as well as featuring several talks from trial sites on how EAA and PMX could be implemented into routine clinical practice after potential regulatory approval of PMX.
- The Company held a Tigris trial Investigator Meeting in conjunction with the 29th
PMX Commercialization:
- 90 patient enrollment interim milestone achieved
- On
February 15, 2024 , Spectral announced that it had reached the 90-patient enrollment threshold and provided written notification toBaxter of this achievement. Subsequently,Baxter exercised its option to maintain exclusive distribution rights and paid Spectral an~C$2 million non-dilutive payment. - Since inception of partnership, funding support from
Baxter has amounted to~C$15 million – comprised of non-dilutive payments and convertible notes subscriptions.
- On
- Amendment of Initial Term of Exclusive Distribution Agreement
- In
February 2024 , the Company andBaxter mutually agreed to amend the initial term of the exclusive distribution agreement to 10 years post-FDA approval; the Company believes the 10-year term provides mutually beneficial runway to maximize PMX commercial economics.
- In
- Commercialization 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 numerousBaxter 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. - 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 theU.S. , is anticipated to be the primary ICU device utilized for PMX treatments on commercial launch.
- In anticipation of a positive Tigris trial outcome, the Company has been working closely with
Funding:
- On
May 9, 2024 , Spectral announced a bought deal private placement of convertible notes for gross proceeds of$8,500,000 .- Based on recent enrollment rates, provides funding beyond full Tigris enrollment of 150 patients.
Financial Review
Revenue for the three-months ended
Operating expenses for the three-months ended
Clinical development and regulatory program costs were
Loss for the three-months ended
The Company concluded the first quarter of 2024 with cash of
The total number of common shares outstanding for the Company was 279,394,428 at
About Spectral
Spectral is a Phase 3 company seeking
PMX is approved for therapeutic use in
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
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:
Capital Markets & Investor Relations | CEO | |
416-962-3300 | ||
am@spinnakercmi.com | cseto@spectraldx.com |
Condensed Interim Consolidated Statements of Financial Position In CAD (000s), except for share and per share data (Unaudited) | |||
Notes | |||
2024 | 2023 | ||
$ | $ | ||
Assets | |||
Current assets | |||
Cash | 2,074 | 2,952 | |
Trade and other receivables | 482 | 186 | |
Inventories | 319 | 366 | |
Prepayments and other assets | 980 | 621 | |
3,855 | 4,125 | ||
Non-current assets | |||
Right-of-use-asset | 536 | 567 | |
Property and equipment | 314 | 326 | |
Intangible asset | 189 | 193 | |
Investment in iDialco | 5 | - | - |
Total assets | 4,894 | 5,211 | |
Liabilities | |||
Current liabilities | |||
Trade and other payables | 2,611 | 2,820 | |
Current portion of contract liabilities | 6 | 496 | 727 |
Current portion of lease liability | 123 | 121 | |
Notes payable | 7 | 278 | 264 |
Derivative Liability | 7 | 7,250 | 6,310 |
10,758 | 10,242 | ||
Non-current liability | |||
Lease liability | 468 | 500 | |
Non-current portion of contract liabilities | 6 | 5,412 | 3,342 |
Notes payable | 7 | 8,393 | 7,676 |
Total liabilities | 25,031 | 21,760 | |
Shareholders' (deficiency) equity | 9 | ||
Share capital | 87,561 | 87,061 | |
Contributed surplus | 8,916 | 8,916 | |
Share-based compensation | 10,547 | 10,385 | |
Warrants | 2,436 | 2,526 | |
Deficit | (129,597) | (125,437) | |
Total shareholders' (deficiency) equity | (20,137) | (16,549) | |
Total liabilities and shareholders' (deficiency) equity | 4,894 | 5,211 |
Condensed Interim Consolidated Statements of Loss and Comprehensive Loss In CAD (000s), except for share and per share data (Unaudited) | |||||
Notes | Three months ended March 31, 2024 | Revised (Refer Note 15) Three months ended 2023 | |||
$ | $ | ||||
Revenue | 668 | 530 | |||
Expenses | |||||
Raw materials and consumables used | 279 | 137 | |||
Salaries and benefits | 13 | 1,000 | 956 | ||
Consulting and professional fees | 925 | 628 | |||
Regulatory and investor relations | 175 | 108 | |||
Travel and entertainment | 76 | 84 | |||
Facilities and communication | 120 | 83 | |||
Insurance | 105 | 87 | |||
Depreciation and amortization | 131 | 61 | |||
Interest expense | 7 | 540 | 247 | ||
Foreign exchange loss | 464 | (51 | ) | ||
Share-based compensation | 177 | (26 | ) | ||
Other expense | (12 | ) | (28 | ) | |
Net loss on joint arrangement | 5 | - | 85 | ||
Fair value adjustment derivative liabilities | 7 | 845 | (746 | ) | |
4,825 | 1,625 | ||||
Loss and comprehensive loss for the period from continuing operations | (4,157 | ) | (1,095 | ) | |
Loss from discontinued operations | 5 | (3 | ) | (43 | ) |
Loss and comprehensive loss for the period | (4,160 | ) | (1,138 | ) | |
Basic and diluted loss from continuing operations per common share | 9 | (0.01 | ) | (0.01 | ) |
Basic and diluted loss from discontinued operations per common share | 9 | 0.00 | 0.00 | ||
Basic and diluted loss per common share | 9 | (0.01 | ) | (0.01 | ) |
Weighted average number of common shares outstanding - basic and diluted | 9 | 279,472,325 | 278,547,804 |
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 | 278,547,804 | 87,050 | 8,773 | 8,908 | 2,490 | (109,744 | ) | (2,523 | ) | |||||||
Loss and comprehensive loss for the year | - | - | - | - | (1,138 | ) | (1,138 | ) | ||||||||
Share-based compensation | 9 | - | - | (26 | ) | - | - | (26 | ) | |||||||
Revised (Refer note 15) Balance, | 278,547,804 | 87,050 | 8,773 | 8,882 | 2,490 | (110,882 | ) | (3,687 | ) | |||||||
RSU released | 28,457 | 11 | (11 | ) | - | - | ||||||||||
Warrants issued | 179 | 179 | ||||||||||||||
Warrants expired | - | - | 143 | - | (143 | ) | - | - | ||||||||
Loss and comprehensive loss for the period | - | - | - | - | - | (14,555 | ) | (14,555 | ) | |||||||
Share-based compensation | - | - | - | 1,514 | - | - | 1,514 | |||||||||
Balance | 278,576,261 | 87,061 | 8,916 | 10,385 | 2,526 | (125,437 | ) | (16,549 | ) | |||||||
Balance | 278,576,261 | 87,061 | 8,916 | 10,385 | 2,526 | (125,437 | ) | (16,549 | ) | |||||||
Warrants exercised | 750,000 | 463 | - | - | (90 | ) | - | 373 | ||||||||
Share options exercised | 68,167 | 37 | - | (15 | ) | - | - | 22 | ||||||||
Loss and comprehensive loss for the period | - | - | - | - | - | (4,160 | ) | (4,160 | ) | |||||||
Share-based compensation | 9 | - | - | - | 177 | - | - | 177 | ||||||||
Balance | 279,394,428 | 87,561 | 8,916 | 10,547 | 2,436 | (129,597 | ) | (20,137 | ) |
Condensed Interim Consolidated Statements of Cash Flows In CAD (000s) (Unaudited) | |||||
Notes | Three months ended 2024 | Revised (Refer note 15) Three months ended 2023 | |||
$ | $ | ||||
Cash flow provided by (used in) | |||||
Operating activities | |||||
Loss for the period | (4,160 | ) | (1,138 | ) | |
Adjustments for: | |||||
Depreciation on right-of-use asset | 31 | 24 | |||
Depreciation on property and equipment | 27 | 24 | |||
Amortization of intangible asset | 4 | 11 | |||
Amortization of deferred financing fee | 69 | 24 | |||
Unrealized foreign exchange gain/loss | 464 | (24 | ) | ||
Interest expense on lease liability | 9 | 10 | |||
Accreted interest on notes payable | 531 | 238 | |||
Share-based compensation (reversal) | 177 | (26 | ) | ||
Net loss on joint venture arrangement | - | 85 | |||
Fair value adjustment derivative liabilities | 846 | (746 | ) | ||
Changes in items of working capital: | |||||
Trade and other receivables | (296 | ) | 174 | ||
Inventories | 47 | (9 | ) | ||
Prepayments and other assets | (359 | ) | (577 | ) | |
Trade and other payables | (453 | ) | (1,371 | ) | |
Contract liabilities | 1,839 | (194 | ) | ||
Net cash used in operating activities | (1,224 | ) | (3,495 | ) | |
Investing activities | |||||
Purchase of property and equipment | (16 | ) | - | ||
Net cash used in investing activities | (16 | ) | - | ||
Financing activities | |||||
Lease liability payments | (33 | ) | (33 | ) | |
Proceeds from share options exercised | 22 | - | |||
Proceeds from warrants exercised | 373 | - | |||
Net cash provided by financing activities | 362 | (33 | ) | ||
Change in cash | (878 | ) | (3,528 | ) | |
Cash, beginning of period | 2,952 | 8,414 | |||
Cash, end of period | 2,074 | 4,886 |
Source:
2024 GlobeNewswire, Inc., source