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Earnings Call Summary | Acurx Pharmaceuticals(ACXP.US) Q1 2024 Earnings Conference

Earnings Call Summary | Acurx Pharmaceuticals(ACXP.US) Q1 2024 Earnings Conference

業績電話會議摘要 | Acurx Pharmicals (ACXP.US) 2024 年第一季度業績會議
moomoo AI ·  05/15 14:31  · 電話會議

The following is a summary of the Acurx Pharmaceuticals, Inc. (ACXP) Q1 2024 Earnings Call Transcript:

以下是Acurx製藥公司(ACXP)2024年第一季度業績電話會議記錄摘要:

Financial Performance:

財務業績:

  • Acurx Pharmaceuticals ended Q1 2024 with a cash balance of $8.9 million, up from $7.5 million at end of December 2023.

  • The ATM Financing Program generated gross proceeds of approximately $4.4 million through an additional sale of 1,121,793 shares.

  • Research and Development (R&D) expenses for the quarter totaled $1.6 million, increasing from $1 million from the same period last year due to a rise in manufacturing related costs.

  • General and administrative expenses were at $2.8 million, compared to $1.9 million for Q1 2023, largely due to a $0.7 million increase in professional fees and a $0.2 million increase in non-cash share-based compensation.

  • Q1 2024 saw a net loss of $4.4 million, or $0.28 per diluted share, an increase from a net loss of $2.9 million, or $0.25 per diluted share from the prior year period.

  • 截至2024年第一季度,Acurx Pharmicals的現金餘額爲890萬美元,高於2023年12月底的750萬美元。

  • 自動櫃員機融資計劃通過額外出售1,121,793股股票產生了約440萬美元的總收益。

  • 由於製造相關成本的上升,該季度的研發(R&D)支出總額爲160萬美元,高於去年同期的100萬美元。

  • 一般和管理費用爲280萬美元,而2023年第一季度爲190萬美元,這主要是由於專業費用增加了70萬美元,非現金股票薪酬增加了20萬美元。

  • 2024年第一季度淨虧損440萬美元,攤薄每股虧損0.28美元,較上年同期淨虧損290萬美元或攤薄每股虧損0.25美元有所增加。

Business Progress:

業務進展:

  • Acurx Pharmaceuticals shared positive comparative microbiology and microbiome data for ibezapolstat, their premier antibiotic candidate, indicating its superiority to the standard treatment, vancomycin.

  • After securing robust preclinical, clinical, and manufacturing data, the company has been approved by the FDA to proceed to Phase 3 trials and follow the regulatory pathway for a new drug application filing for marketing approval in the U.S.

  • The company also received approval from the European Medicines Agency for their SME recognition application in Europe.

  • Planning for two Phase 3 trials is set to begin in Q4 2024, with estimated total enrollments of 900 Modified Intent-to-Treat (MITT) patients.

  • A strategic transaction, possibly including a partnership for further development and potential commercialization of ibezapolstat, is being actively sought by the company.

  • The continuation of a blinded trial and discussions on the PASTEUR Act, which if approved, could unlock additional funding for late-stage clinical trials, are notable undertakings by the company.

  • Acurx Pharmicals分享了其首屈一指的抗生素候選藥物ibezapolstat的正面比較微生物學和微生物組數據,這表明其優於標準療法萬古黴素。

  • 在獲得可靠的臨床前、臨床和生產數據後,該公司已獲得 FDA 的批准,可以繼續進行三期試驗,並遵循監管途徑在美國申請上市批准的新藥申請。

  • 該公司在歐洲的中小企業認可申請也獲得了歐洲藥品管理局的批准。

  • 兩項3期試驗的計劃將於2024年第四季度開始,估計總入組人數爲900名改良意向治療(MITT)患者。

  • 該公司正在積極尋求一項戰略交易,可能包括就ibezapolstat的進一步開發和潛在商業化建立合作伙伴關係。

  • 繼續進行盲目試驗和討論《巴斯德法案》是該公司取得的顯著成果,該法案如果獲得批准,可能會爲後期臨床試驗騰出更多資金。

更多詳情: Acurx 製藥 IR

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