Iterum Therapeutics Reports Fourth Quarter and Full Year 2022 Financial Results
Iterum Therapeutics (Nasdaq: ITRM) reported its financial results for Q4 and full year 2022, showing a net loss of $5.1 million for Q4 and $44.4 million for the entire year, improving from a net loss of $4.2 million and $91.6 million in 2021. The company focuses on developing oral and IV antibiotics to combat multi-drug resistant infections. Enrollment in the REASSURE clinical trial for uUTI treatment is ongoing, with an interim analysis expected later in 2023. Cash reserves as of December 31, 2022, stand at $60.8 million, projected to sustain operations until mid-2024. The company also received two new patents extending its portfolio until at least 2039.
- Ongoing enrollment in the pivotal REASSURE trial, significant step towards NDA resubmission.
- Cash reserves of $60.8 million expected to fund operations until mid-2024.
- Issuance of two new patents extending market exclusivity until at least 2039.
- Shareholder lawsuit dismissed with prejudice, removing potential legal risks.
- Net loss increased to $44.4 million for 2022 from $91.6 million in 2021, indicating ongoing financial challenges.
- R&D expenses significantly increased to $17.6 million driven by trial costs, raising concern over cash burn.
--Registration Trial for uUTI Ongoing and On Track--
--Cash Runway until Mid-2024--
--Company to host conference call today at 8:30amET--
DUBLIN, Ireland and CHICAGO, March 16, 2023 (GLOBE NEWSWIRE) -- Iterum Therapeutics plc (Nasdaq: ITRM), a clinical-stage pharmaceutical company focused on developing next generation oral and IV antibiotics to treat infections caused by multi-drug resistant pathogens in both community and hospital settings, today reported financial results for the fourth quarter and year ended December 31, 2022.
“We made significant progress in 2022 to move the clinical development of oral sulopenem forward leading to a potential resubmission of our new drug application (“NDA”) next year,” said Corey Fishman, Iterum’s Chief Executive Officer. “Enrollment in our REASSURE trial, which is being conducted under a Special Protocol Assessment (“SPA”) agreement with the U.S. Food and Drug Administration (“FDA”), is expected to be completed in the first half of 2024.”
Highlights and Recent Events
- Enrollment in REASSURE Clinical Trial Ongoing: Iterum began enrollment in its pivotal Phase 3 clinical trial, REASSURE (REnewed ASsessment of Sulopenem in uUTI caused by Resistant Enterobacterales), for the treatment of uncomplicated urinary tract infections (“uUTI”) in adult women in October 2022. Enrollment is ongoing and expected to be completed in the first half of 2024. An interim analysis at
50% patient enrollment is expected to occur in the second half of 2023. This trial is being conducted under a SPA agreement with the FDA. The SPA agreement provides that the design and planned analysis of the trial, as set out in the protocol submitted to the FDA, adequately addresses the objectives necessary to support the potential resubmission of Iterum’s NDA for oral sulopenem.
- Two New U.S. Patents Issued: The United States Patent and Trademark Office has issued Iterum two new patents: 1) US Patent No. 11,478,428, directed to the composition of the bilayer tablet of sulopenem etzadroxil and probenecid (“oral sulopenem”) and its related uses, and 2) US Patent No. 11,554,112 directed to the method of use of oral sulopenem in treating multiple diseases, including uncomplicated urinary tract infections. These U.S. patents are scheduled to expire no earlier than 2039, excluding any additional term for patent adjustments or patent term extensions. Existing patent protection for sulopenem etzadroxil is scheduled to expire in 2029, subject to potential extension. Iterum’s patent portfolio also contains pending patent applications outside the U.S., including Europe and China, submitted following receipt of the Written Opinion of the International Search Authority indicating that several claims directed to the composition of the bilayer tablet of oral sulopenem are novel and inventive.
- Shareholder Lawsuit Dismissed: On January 25, 2023, the putative class action lawsuit filed against Iterum, its Chief Executive Officer and Chief Financial Officer in the United States District Court for the Northern District of Illinois on August 5, 2021, was dismissed and cannot be brought back to court (dismissed with prejudice).
Fourth Quarter and Full Year 2022 Financial Results
Cash, cash equivalents and short-term investments were
Research and development (R&D) expenses for the fourth quarter and full year 2022 were
General and administrative (G&A) expenses for the fourth quarter and full year 2022 were
2023.
Adjustments to the fair value of derivatives for the fourth quarter and full year 2022 were
Cancellation of share options for the full year 2022 was
Net loss for the fourth quarter and full year 2022 was
Conference Call Details
- Iterum will host a conference call today, Thursday, March 16, 2023 at 8:30 a.m. Eastern Time. The dial-in information for the call is as follows: United States: 1 844 200 6205; International: 1 929 526 1599; Access code: 846586
About Iterum Therapeutics plc
Iterum Therapeutics plc is a clinical-stage pharmaceutical company dedicated to developing differentiated anti-infectives aimed at combatting the global crisis of multi-drug resistant pathogens to significantly improve the lives of people affected by serious and life-threatening diseases around the world. Iterum is currently advancing its first compound, sulopenem, a novel penem anti-infective compound, in Phase 3 clinical development with an oral formulation. Sulopenem also has an IV formulation. Sulopenem has demonstrated potent in vitro activity against a wide variety of gram-negative, gram-positive and anaerobic bacteria resistant to other antibiotics. Iterum has received Qualified Infectious Disease Product (QIDP) and Fast Track designations for its oral and IV formulations of sulopenem in seven indications. For more information, please visit http://www.iterumtx.com.
Non-GAAP Financial Measures
To supplement Iterum’s financial results presented in accordance with U.S. generally accepted accounting principles (“GAAP”), Iterum presents non-GAAP net loss and non-GAAP net loss per share to exclude from reported GAAP net loss and GAAP net loss per share, intangible asset amortization (
Iterum believes that the presentation of non-GAAP net loss and non-GAAP net loss per share, when viewed with its results under GAAP and the accompanying reconciliation, provides useful supplementary information to, and facilitates additional analysis by, investors, analysts, and Iterum’s management in assessing Iterum’s performance and results from period to period. These non-GAAP financial measures closely align with the way management measures and evaluates Iterum’s performance. These non-GAAP financial measures should be considered in addition to, and not a substitute for, or superior to, net (loss) / income or other financial measures calculated in accordance with GAAP. Non-GAAP net loss and non-GAAP net loss per share are not based on any standardized methodology prescribed by GAAP and represents GAAP net (loss) / income, which is the most directly comparable GAAP measure, adjusted to exclude intangible asset amortization; share-based compensation expense; the non-cash expense for the cancellation of share options; the interest expense associated with accrued interest on the Exchangeable Notes payable in cash, shares or a combination of both upon exchange, redemption or at the Maturity Date, whichever is earlier; the non-cash amortization of the Exchangeable Notes and Royalty- Linked Notes; and the non-cash adjustments to the fair value of derivatives and Royalty-Linked Notes for the three and twelve months ended December 31, 2022 and December 31, 2021. Because of the non-standardized definitions of non-GAAP financial measures, non-GAAP net loss and non-GAAP net loss per share used by Iterum Therapeutics in this press release and accompanying tables has limits in its usefulness to investors and may be calculated differently from, and therefore may not be directly comparable to, similarly titled measures used by other companies. A reconciliation of non-GAAP net loss to GAAP net (loss) / income and non-GAAP net loss per share to GAAP net (loss) / income per share have been provided in the tables included in this press release.
1 Definition and reconciliations of applicable GAAP reported to non-GAAP adjusted information are included at the end of this press release
Special Note Regarding Forward Looking Statements
This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. These forward-looking statements include, without limitation, statements regarding Iterum’s plans, strategies and prospects for its business, including the development, therapeutic and market potential of sulopenem, the timing, conduct, progress and results of Iterum’s ongoing REASSURE clinical trial, the expected timing of resubmission of the NDA, the term and coverage provided by Iterum’s patent and other intellectual property rights, and the sufficiency of Iterum’s cash resources. In some cases, forward-looking statements can be identified by words such as “may,” “believes,” “intends,” “seeks,” “anticipates,” “plans,” “estimates,” “expects,” “should,” “assumes,” “continues,” “could,” “would,” “will,” “future,” “potential” or the negative of these or similar terms and phrases. Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause Iterum’s actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Forward-looking statements include all matters that are not historical facts. Actual future results may be materially different from what is expected due to factors largely outside Iterum’s control, including uncertainties inherent in the design, initiation and conduct of clinical and non-clinical development, including the REASSURE clinical trial, availability and timing of data from the REASSURE clinical trial, changes in regulatory requirements or decisions of regulatory authorities, the timing or likelihood of regulatory filings and approvals, including the potential resubmission of the NDA for oral sulopenem, changes in public policy or legislation, commercialization plans and timelines, if oral sulopenem is approved, the actions of third-party clinical research organizations, suppliers and manufacturers, the accuracy of Iterum’s expectations regarding how far into the future Iterum’s cash on hand will fund Iterum’s ongoing operations, , Iterum’s ability to maintain its listing on the Nasdaq Capital Market, risks and uncertainties concerning the outcome, impact, effects and results of Iterum’s evaluation of corporate, strategic, financial and financing alternatives, including the terms, timing, structure, value, benefits and costs of any corporate, strategic, financial or financing alternative and Iterum’s ability to complete one at all and other factors discussed under the caption “Risk Factors” in its Annual Report on Form 10-K filed with the SEC on March 16, 2023, and other documents filed with the SEC from time to time. Forward-looking statements represent Iterum’s beliefs and assumptions only as of the date of this press release. Except as required by law, Iterum assumes no obligation to update these forward-looking statements publicly, or to update the reasons actual results could differ materially from those anticipated in the forward-looking statements, even if new information becomes available in the future.
Investor Contact:
Judy Matthews
Chief Financial Officer 312-778-6073
IR@iterumtx.com
ITERUM THERAPEUTICS PLC | |||||||||||||||
Condensed Consolidated Statement of Operations | |||||||||||||||
(In thousands except share and per share data) | |||||||||||||||
(Unaudited) | |||||||||||||||
For the three months ended | Year ended | ||||||||||||||
December 31, | December 31, | ||||||||||||||
2022 | 2021 | 2022 | 2021 | ||||||||||||
Operating expenses: | |||||||||||||||
Research and development | (5,840 | ) | (3,702 | ) | (17,617 | ) | (10,712 | ) | |||||||
General and administrative | (2,086 | ) | (3,127 | ) | (12,766 | ) | (13,825 | ) | |||||||
Total operating expenses | (7,926 | ) | (6,829 | ) | (30,383 | ) | (24,537 | ) | |||||||
Operating loss | (7,926 | ) | (6,829 | ) | (30,383 | ) | (24,537 | ) | |||||||
Interest income / (expense), net | 80 | (772 | ) | (2,361 | ) | (5,553 | ) | ||||||||
Adjustments to fair value of derivatives | 2,960 | 3,562 | 5,458 | (60,964 | ) | ||||||||||
Cancellation of share options | - | - | (17,350 | ) | - | ||||||||||
Other (expense) income, net | (103 | ) | 28 | 503 | 195 | ||||||||||
Income tax expense | (101 | ) | (171 | ) | (301 | ) | (705 | ) | |||||||
Net loss attributable to ordinary shareholders | $ | (5,090 | ) | $ | (4,182 | ) | $ | (44,434 | ) | $ | (91,564 | ) | |||
Net loss per share attributable to ordinary shareholders – basic and diluted | $ | (041 | ) | $ | (0.34 | ) | $ | (3.63 | ) | $ | (8.41 | ) | |||
Weighted average ordinary shares outstanding – basic and diluted | 12,294,865 | 12,185,019 | 12,236,607 | 10,891,178 | |||||||||||
Reconciliation of non-GAAP net loss to GAAP net loss | |||||||||||||||
Net loss - GAAP | $ | (5,090 | ) | $ | (4,182 | ) | $ | (44,434 | ) | $ | (91,564 | ) | |||
Intangible asset amortization | 429 | 1,713 | 1,716 | 1,713 | |||||||||||
Share based compensation | 457 | 1,967 | 4,758 | 4,319 | |||||||||||
Cancellation of share options | - | - | 17,350 | - | |||||||||||
Interest expense - accrued interest and amortization on Exchangeable Notes and Royalty-Linked Notes | 786 | 796 | 3,154 | 5,175 | |||||||||||
Adjustments to fair value of derivatives | (2,960 | ) | (3,562 | ) | (5,458 | ) | 60,964 | ||||||||
Non-GAAP net loss | $ | (6,378 | ) | $ | (3268 | ) | $ | (22,914 | ) | $ | (19,393 | ) | |||
Net loss per share attributable to ordinary shareholders – basic and diluted | $ | (0.41 | ) | $ | (0.34 | ) | $ | (3.63 | ) | $ | (8.41 | ) | |||
Non-GAAP net loss per share attributable to ordinary shareholders – basic and diluted | $ | (0.52 | ) | $ | (0.27 | ) | $ | (1.87 | ) | $ | (1.78) |
ITERUM THERAPEUTICS PLC | ||||
Condensed Consolidated Balance Sheet Data (In thousands) | ||||
(Unaudited) | ||||
As of | As of | |||
December 31, | December 31, | |||
2022 | 2021 | |||
Cash, cash equivalents and short-term investments | $ | 60,838 | $ | 81,344 |
Other assets | 5,995 | 10,165 | ||
Total assets | $ | 66,833 | $ | 91,509 |
Long-term debt, less current portion | $ | 10,094 | $ | 6,930 |
Royalty-linked notes | 18,372 | 17,968 | ||
Derivative liabilities | 196 | 6,058 | ||
Other liabilities | 10,172 | 10,319 | ||
Total liabilities | 38,834 | 41,275 | ||
Total shareholders' equity | 27,999 | 50,234 | ||
Total liabilities and shareholders' equity | $ | 66,833 | $ | 91,509 |
FAQ
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