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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

财报电话会议摘要 | Acurx Pharmicals (ACXP.US) 2024 年第一季度财报会议
moomoo AI ·  05/15 14:31  · 电话会议

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

以下是Acurx制药公司(ACXP)2024年第一季度财报电话会议记录摘要:

Financial Performance:

财务业绩:

  • 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的现金余额为890万美元,高于2023年12月底的750万美元。

  • 自动柜员机融资计划通过额外出售1,121,793股股票产生了约440万美元的总收益。

  • 由于制造相关成本的上升,该季度的研发(R&D)支出总额为160万美元,高于去年同期的100万美元。

  • 一般和管理费用为280万美元,而2023年第一季度为190万美元,这主要是由于专业费用增加了70万美元,非现金股票薪酬增加了20万美元。

  • 2024年第一季度净亏损440万美元,摊薄每股亏损0.28美元,较上年同期净亏损290万美元或摊薄每股亏损0.25美元有所增加。

Business Progress:

业务进展:

  • 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选药物ibezapolstat的正面比较微生物学和微生物组数据,这表明其优于标准疗法万古霉素。

  • 在获得可靠的临床前、临床和生产数据后,该公司已获得 FDA 的批准,可以继续进行三期试验,并遵循监管途径在美国申请上市批准的新药申请。

  • 该公司在欧洲的中小企业认可申请也获得了欧洲药品管理局的批准。

  • 两项3期试验的计划将于2024年第四季度开始,估计总入组人数为900名改良意向治疗(MITT)患者。

  • 该公司正在积极寻求一项战略交易,可能包括就ibezapolstat的进一步开发和潜在商业化建立合作伙伴关系。

  • 继续进行盲目试验和讨论《巴斯德法案》是该公司取得的显著成果,该法案如果获得批准,可能会为后期临床试验腾出更多资金。

更多详情: Acurx 制药 IR

Tips: This article is generated by AI. The accuracy of the content can not be fully guaranteed. For more comprehensive details, please refer to the IR website. The article is only for investors' reference without any guidance or recommendation suggestions.

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