Iterum Therapeutics Regains Full Nasdaq Compliance
Iterum Therapeutics (Nasdaq: ITRM) has regained full compliance with Nasdaq listing requirements, resolving its previous deficiency under Listing Rule 5550(b). The company received written confirmation from Nasdaq's Listing Qualifications Staff, and the previously scheduled hearing before the Hearings Panel on November 21 has been cancelled. As a result, Iterum will continue to be traded on The Nasdaq Capital Market. The company focuses on developing next-generation oral and IV antibiotics for treating multi-drug resistant pathogen infections in both community and hospital settings.
Iterum Therapeutics (Nasdaq: ITRM) ha riacquisito la piena conformità ai requisiti di quotazione del Nasdaq, risolvendo la sua precedente carenza ai sensi della Regola di Quotazione 5550(b). L'azienda ha ricevuto una conferma scritta dal personale delle Qualifiche di Quotazione del Nasdaq, e l'udienza precedentemente programmata davanti al Panell degli Auditi il 21 novembre è stata cancellata. Di conseguenza, Iterum continuerà a essere quotata sul Nasdaq Capital Market. L'azienda si concentra sullo sviluppo di antibiotici orali e IV di nuova generazione per il trattamento delle infezioni da patogeni multi-resistenti sia in contesti comunitari che ospedalieri.
Iterum Therapeutics (Nasdaq: ITRM) ha recuperado el cumplimiento total de los requisitos de cotización del Nasdaq, resolviendo su anterior deficiencia bajo la Regla de Cotización 5550(b). La empresa recibió una confirmación escrita del personal de Calificaciones de Cotización del Nasdaq, y la audiencia programada previamente ante el Panel de Audiencias para el 21 de noviembre ha sido cancelada. Como resultado, Iterum continuará siendo negociada en el Nasdaq Capital Market. La empresa se enfoca en el desarrollo de antibióticos orales e IV de nueva generación para tratar infecciones por patógenos resistentes a múltiples fármacos tanto en comunidades como en entornos hospitalarios.
Iterum Therapeutics (Nasdaq: ITRM)는 나스닥 상장 요건을 완전히 충족하여 이전의 5550(b) 상장 규정 부적합 문제를 해결했습니다. 회사는 나스닥의 상장 자격 직원으로부터 서면 확인을 받았으며, 11월 21일에 예정되었던 청문회가 취소되었습니다. 그 결과, Iterum은 나스닥 캐피탈 마켓에서 계속 거래될 것입니다. 이 회사는 지역사회와 병원 환경에서 다제내성 병원체 감염을 치료하기 위한 차세대 경구 및 IV 항생제 개발에 집중하고 있습니다.
Iterum Therapeutics (Nasdaq: ITRM) a retrouvé sa pleine conformité aux exigences de cotation du Nasdaq, résolvant ainsi son précédent manquement en vertu de la règle de cotation 5550(b). L'entreprise a reçu une confirmation écrite du personnel des Qualifications de Cotation du Nasdaq, et l'audience initialement prévue devant le Comité des Audiences le 21 novembre a été annulée. En conséquence, Iterum continuera d'être coté sur le Nasdaq Capital Market. L'entreprise se concentre sur le développement d'antibiotiques oraux et IV de nouvelle génération pour traiter les infections causées par des pathogènes multi-résistants tant dans les collectivités que dans les hôpitaux.
Iterum Therapeutics (Nasdaq: ITRM) hat die vollständige Einhaltung der Nasdaq-Börsenanforderungen wiedererlangt und somit seine vorherige Mängel gemäß der Listing-Regel 5550(b) behoben. Das Unternehmen erhielt eine schriftliche Bestätigung vom Listing Qualifications Staff von Nasdaq, und die zuvor angesetzte Anhörung vor dem Hearings Panel am 21. November wurde abgesagt. Infolgedessen wird Iterum weiterhin am Nasdaq Capital Market gehandelt. Das Unternehmen konzentriert sich auf die Entwicklung von Antibiotika der nächsten Generation zur oralen und intravenösen Anwendung zur Behandlung von Infektionen durch multiresistente Krankheitserreger in Gemeinschafts- und Krankenhausumgebungen.
- Regained full Nasdaq compliance, avoiding potential delisting
- Maintains Nasdaq Capital Market listing status
- None.
Insights
The regaining of Nasdaq compliance is a important development for Iterum Therapeutics, removing a significant near-term risk of delisting. For a small-cap biotech company with a market cap of just
Iterum will Continue to be Listed and Traded on the Nasdaq Stock Market
DUBLIN and CHICAGO, Nov. 21, 2024 (GLOBE NEWSWIRE) -- Iterum Therapeutics plc (Nasdaq: ITRM), (the Company), a company focused on delivering next generation oral and IV antibiotics to treat infections caused by multi-drug resistant pathogens in both community and hospital settings, today announced receipt of written notice from the Listing Qualifications Staff of The Nasdaq Stock Market LLC informing the Company that its deficiency under Listing Rule 5550(b) has been cured and that the Company is in compliance with applicable continued listing requirements.
Based on the foregoing, the previously scheduled Nasdaq hearing before the Hearings Panel on November 21, has been cancelled. The Company will continue to be traded on The Nasdaq Capital Market.
“We are pleased to have addressed this very important matter to us and our shareholders,” said Corey Fishman, Iterum’s Chief Executive Officer. “We will continue to do everything we can to adhere to the Nasdaq listing requirements as we move forward with executing our business strategy.”
About Iterum Therapeutics plc
Iterum Therapeutics plc is focused on delivering 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 advancing the development of its first compound, sulopenem, a novel penem anti-infective compound, with an oral formulation and 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 approval of its NDA for ORLYNVAH™ (oral sulopenem) for the treatment of uncomplicated urinary tract infections caused by the designated microorganisms Escherichia coli, Klebsiella pneumoniae, or Proteus mirabilis in adult women with limited or no alternative oral antibacterial treatment options by the U.S. Food and Drug Administration and 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 www.iterumtx.com.
About ORLYNVAH™
ORLYNVAH™ is a novel oral penem antibiotic for the treatment of uUTI. ORLYNVAH™ possesses potent activity against species of Enterobacterales including those that encode extended spectrum beta-lactamase (ESBL) or AmpC-type beta-lactamases that confer resistance to third generation cephalosporins.
Cautionary 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. 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 risks and uncertainties concerning the outcome, impact, effects and results of Iterum’s evaluation of strategic alternatives, including the terms, timing, structure, value, benefits and costs of any strategic alternatives, Iterum’s ability to complete a strategic alternative transaction, Iterum’s ability to successfully prepare and implement commercialization plans for ORLYNVAH™ with a commercial partner or directly, including the Iterum’s ability to build and maintain a sales force and prepare for commercial launch of ORLYNVAH™, if Iterum is unsuccessful at entering into or completing a strategic transaction, the ability of shareholders and other stakeholders to realize any value or recovery as part of a wind down process if Iterum is unsuccessful at entering into or completing a strategic transaction or preparing and implementing commercialization plans for ORLYNVAH™, the market opportunity for and the potential market acceptance of ORLYNVAH™ for uUTIs caused by certain designated microorganisms in adult women who have limited or no alternative oral antibacterial treatment options, uncertainties inherent in the conduct of clinical and non-clinical development, changes in regulatory requirements or decisions of regulatory authorities, the timing or likelihood of regulatory filings and approvals, changes in public policy or legislation, commercialization plans and timelines, 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 and other factors discussed under the caption “Risk Factors” in its Quarterly Report on Form 10-Q filed with the SEC on November 14, 2024, 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
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