Iterum Therapeutics Reports Second Quarter 2021 Financial Results and Provides Business Update
Iterum Therapeutics (ITRM) reported its Q2 2021 financial results, noting a net income of $7.8 million, significantly improved from a net loss of $12.5 million in Q2 2020. The increase is attributed to a non-cash adjustment related to its Royalty-Linked Notes. Following an FDA Complete Response Letter in July, Iterum is preparing for a Type A meeting with the FDA regarding the approval pathway for oral sulopenem, anticipated by late Q3 2021. The company maintains a strong cash position, with $91.4 million on hand, sufficient to fund operations into the second half of 2023.
- Q2 2021 net income of $7.8 million compared to a net loss of $12.5 million in Q2 2020.
- Cash reserves of $91.4 million expected to fund operations into the second half of 2023.
- FDA's Complete Response Letter indicates that additional data and another clinical trial are needed before approval can be considered.
--Type A meeting with FDA expected late Q3 to define pathway to potential approval for Oral Sulopenem following July’s Complete Response Letter--
--Cash Runway into Second Half of 2023--
--Company to host conference call today at 8:30am ET--
DUBLIN, Ireland and CHICAGO, Aug. 13, 2021 (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 second quarter ended June 30, 2021.
“Despite our disappointment with the FDA’s Complete Response Letter (“CRL”), we’ve begun preparations for the Type A meeting with the FDA expected later this quarter and we hope to receive adequate guidance and agreement with the FDA on a path forward that will lead to resubmission of our New Drug Application (“NDA”) as quickly as possible,” said Corey Fishman, Chief Executive Officer.
Highlights and Recent Events
- FDA completes review of NDA: On July 23, 2021, we received a CRL from the U.S. Food and Drug Administration (“FDA”) with respect to our NDA for oral sulopenem for the treatment of uncomplicated urinary tract infections in patients with a quinolone non-susceptible organism, stating that the FDA could not approve the NDA in its present form. The CRL provided that additional data are necessary to support approval of oral sulopenem and recommended that we conduct at least one additional adequate and well-controlled clinical trial, potentially using a different comparator drug. Additionally, the FDA recommended that we conduct further non-clinical investigation to determine the optimal dosing regimen, although the FDA stated that this recommendation does not raise an approvability issue. We plan to have a Type A meeting with the FDA to identify the next steps as to the potential additional clinical and non-clinical work to support a potential resubmission of the NDA for approval of oral sulopenem. The meeting is expected to take place near the end of the third quarter.
- Cash runway into second half of 2023: Based on the current operating plan and subject to final determination of the design and planned conduct of potential additional clinical and non-clinical development for sulopenem, we believe that we are well positioned financially to fund operations into the second half of 2023. Following receipt of the CRL, in order to reduce operating expenses and conserve cash resources, we halted any remaining pre-commercial activities for oral sulopenem and plan to limit spending to essential costs required in connection with the potential resubmission of the NDA. If and when we believe regulatory approval of oral sulopenem appears likely, we plan to resume pre-commercialization activities and negotiations on a definitive agreement for commercialization services. As of June 30, 2021, we had approximately 182.6 million ordinary shares outstanding.
Second Quarter 2021 Financial Results
As of June 30, 2021, Iterum had cash, cash equivalents and short-term investments of
Research and development expenses for the second quarter of 2021 were
General and administrative (G&A) expenses for the second quarter of 2021 were
Adjustments to the fair value of derivatives for the second quarter 2021 were
For the second quarter of 2021, Iterum reported net income of
Upcoming Investor Presentation
- Corporate presentation at the H.C. Wainwright 23rd Annual Global Investment Conference in New York, NY on September 13, 2021 at 12:00pm ET
Conference Call Details
- Iterum will host a conference call today, Friday, August 13, 2021 at 8:30 a.m. Eastern Time. The dial-in information for the call is as follows: United States: 1 844 200 6205 (Toll Free); United States (Local): 1 646 904 5544 (Local); All Other Locations: + 44 208 0682 558; Access code: 096194
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 Therapeutics is advancing its first compound, sulopenem, a novel penem anti-infective compound, in Phase 3 clinical development with oral and IV formulations. Sulopenem has demonstrated potent in vitro activity against a wide variety of gram-negative, gram-positive and anaerobic bacteria resistant to other antibiotics. Iterum Therapeutics 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 Therapeutics’ financial results presented in accordance with U.S. generally accepted accounting principles (“GAAP”), Iterum Therapeutics presents non-GAAP adjusted net loss and non-GAAP net loss per share to exclude from reported GAAP net income/(loss) and GAAP net income/(loss) per share, the interest expense associated with accrued interest on the Exchangeable Notes (“ ENs”), payable in cash, shares or a combination of both upon exchange, redemption or at January 31, 2025 (“the Maturity Date”), whichever is earlier (
Iterum Therapeutics believes that the presentation of non-GAAP adjusted 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 Therapeutics’ management in assessing Iterum Therapeutics’ performance and results from period to period. These non-GAAP financial measures closely align with the way management measures and evaluates Iterum Therapeutics’ performance. These non-GAAP financial measures should be considered in addition to, and not a substitute for, or superior to, net income/(loss) or other financial measures calculated in accordance with GAAP. Non-GAAP adjusted net loss and non-GAAP net loss per share are not based on any standardized methodology prescribed by GAAP and represents GAAP net income/(loss), which is the most directly comparable GAAP measure, adjusted to exclude the interest expense associated with accrued interest on the ENs 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 ENs and Royalty-Linked Notes; one-time, non-capitalized financing transaction costs and the non-cash adjustments to the fair value of derivatives for the three and six months ended June 30, 2021 and June 30, 2020. Because of the non-standardized definitions of non-GAAP financial measures, non-GAAP adjusted net loss and non-GAAP net loss per share used by Iterum Therapeutics in the accompanying press release and tables therein 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 adjusted net loss to GAAP net income/(loss) and non-GAAP net loss per share to GAAP net income/(loss) per share have been provided in the tables included in the accompanying press release.
Forward Looking Statements
This press release contains forward-looking statements. These forward-looking statements include, without limitation, statements regarding the Company’s plans, strategies and prospects for its business, including with respect to planned interactions and communications with the FDA, the Company’s expectations with regard to its ability to resolve the matters set forth in the CRL and obtain approval for oral sulopenem, the conduct of potential future clinical and non-clinical development of sulopenem, the potential timing for resuming pre-commercialization activities, and the sufficiency of the Company’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 the Company’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 the Company’s control, including uncertainties inherent in the initiation and conduct of clinical and non-clinical development, including any potential additional clinical trials and non-clinical development that may be conducted in response to the CRL, availability and timing of data from such potential clinical and non-clinical development, changes in regulatory requirements or decisions of regulatory authorities, the timing or likelihood of regulatory filings and approvals, including any potential resubmission of the NDA, 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 the Company’s expectations regarding how far into the future the Company’s cash on hand will fund the Company’s ongoing operations, the impact of COVID-19 and related responsive measures thereto, risks and uncertainties concerning the outcome, impact, effects and results of the Company’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 the Company’s ability to complete one at all and other factors discussed under the caption “Risk Factors” in its Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission (the “SEC”) on August 13, 2021, and other documents filed with the SEC from time to time. Forward-looking statements represent the Company’s beliefs and assumptions only as of the date of this press release. Except as required by law, the Company 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) | ||||||||||||||||
| Three months ended June 30, | Six months ended June 30, | |||||||||||||||
| 2021 | 2020 | 2021 | 2020 | |||||||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | (2,714 | ) | (5,043 | ) | (5,165 | ) | (14,786 | ) | ||||||||
| General and administrative | (4,273 | ) | (3,210 | ) | (7,669 | ) | (6,361 | ) | ||||||||
| Total operating expenses | (6,987 | ) | (8,253 | ) | (12,834 | ) | (21,147 | ) | ||||||||
| Operating loss | (6,987 | ) | (8,253 | ) | (12,834 | ) | (21,147 | ) | ||||||||
| Interest expense, net | (980 | ) | (4,075 | ) | (3,932 | ) | (6,671 | ) | ||||||||
| Financing transaction costs | — | — | — | (2,130 | ) | |||||||||||
| Adjustments to fair value of derivatives | 15,794 | (12 | ) | (74,309 | ) | 1,667 | ||||||||||
| Other income / (expense), net | 93 | (3 | ) | 134 | (41 | ) | ||||||||||
| Income tax expense | (122 | ) | (178 | ) | (182 | ) | (299 | ) | ||||||||
| Net income/ (loss) attributable to ordinary shareholders | $ | 7,798 | $ | (12,521 | ) | $ | (91,123 | ) | $ | (28,621 | ) | |||||
| Net income / (loss) per share attributable to ordinary shareholders – basic | $ | 0.04 | $ | (0.80 | ) | $ | (0.63 | ) | $ | (1.87 | ) | |||||
| Net income / (loss) per share attributable to ordinary shareholders – diluted | $ | 0.04 | $ | (0.80 | ) | $ | (0.63 | ) | $ | (1.87 | ) | |||||
| Weighted average ordinary shares outstanding – basic | 180,017,313 | 15,614,767 | 144,608,227 | 15,295,141 | ||||||||||||
| Weighted average ordinary shares outstanding – diluted | 204,600,645 | 15,614,767 | 144,608,227 | 15,295,141 | ||||||||||||
| Reconciliation of non-GAAP net income / (loss) to GAAP net loss | ||||||||||||||||
| Net income / (loss) - GAAP | $ | 7,798 | $ | (12,521 | ) | $ | (91,123 | ) | $ | (28,621 | ) | |||||
| Interest expense - accrued interest and amortization on Exchangeable Notes and Royalty-Linked Notes | 835 | 3,704 | 3,583 | 5,970 | ||||||||||||
| Financing transaction costs - not capitalized | — | — | — | 2,130 | ||||||||||||
| Adjustments to fair value of derivatives | (15,794 | ) | 12 | 74,309 | (1,667 | ) | ||||||||||
| Non-GAAP net loss | $ | (7,161 | ) | $ | (8,805 | ) | $ | (13,231 | ) | $ | (22,188 | ) | ||||
| Net income / (loss) per share attributable to ordinary shareholders – basic | $ | 0.04 | $ | (0.80 | ) | $ | (0.63 | ) | $ | (1.87 | ) | |||||
| Net income / (loss) per share attributable to ordinary shareholders – diluted | $ | 0.04 | $ | (0.80 | ) | $ | (0.63 | ) | $ | (1.87 | ) | |||||
| Non-GAAP net loss per share attributable to ordinary shareholders – basic and diluted | $ | (0.04 | ) | $ | (0.56 | ) | $ | (0.09 | ) | $ | (1.45 | ) | ||||
| ITERUM THERAPEUTICS PLC | ||||||||||||||||
| Condensed Consolidated Balance Sheet Data | ||||||||||||||||
| (In thousands) | ||||||||||||||||
| (Unaudited) | ||||||||||||||||
| As of | As of | |||||||||||||||
| June 30, | December 31, | |||||||||||||||
| 2021 | 2020 | |||||||||||||||
| Cash, cash equivalents and short-term investments | $ | 91,440 | $ | 14,508 | ||||||||||||
| Other assets | 14,605 | 18,284 | ||||||||||||||
| Total assets | $ | 106,045 | $ | 32,792 | ||||||||||||
| Long-term debt, less current portion | $ | 5,339 | 22,462 | |||||||||||||
| Royalty-linked notes, less current portion | 15,315 | 13,389 | ||||||||||||||
| Derivative liabilities | 21,864 | 28,865 | ||||||||||||||
| Other liabilities | 16,332 | 18,635 | ||||||||||||||
| Total liabilities | $ | 58,850 | $ | 83,351 | ||||||||||||
| Total shareholders' equity / (deficit ) | $ | 47,195 | $ | (50,559 | ) | |||||||||||
| Total liabilities and shareholders' equity / (deficit) | $ | 106,045 | $ | 32,792 | ||||||||||||
1 Reconciliations of applicable GAAP reported to non-GAAP adjusted information are included at the end of this press release
FAQ
What are the key financial results reported by Iterum Therapeutics for Q2 2021?
When is the Type A meeting with the FDA expected for Iterum Therapeutics?
What is the current cash position of Iterum Therapeutics?
What does the Complete Response Letter from the FDA mean for Iterum Therapeutics?
