Earnings Call Summary | Co-diagnostics(CODX.US) Q3 2024 Earnings Conference
Earnings Call Summary | Co-diagnostics(CODX.US) Q3 2024 Earnings Conference
The following is a summary of the Co-Diagnostics, Inc. (CODX) Q3 2024 Earnings Call Transcript:
以下是Co-Diagnostics, Inc. (CODX) 2024年第三季度业绩会的摘要:
Financial Performance:
财务表现:
Total revenue for Q3 2024 decreased to $0.6 million from $2.5 million in the same period last year.
Gross profit for the quarter decreased to $0.3 million from $2.2 million year over year.
Net loss for the quarter increased to $9.7 million, or a loss of $0.32 per fully diluted share, compared to a net loss of $6.0 million, or $0.20 per fully diluted share in the prior year.
2024年第三季度的营业收入从去年同期的250万美元减少到60万美元。
本季度的毛利润从去年同期的220万美元减少到30万美元。
本季度的净亏损增加至970万美元,或每股摊薄亏损0.32美元,而去年同期的净亏损为600万美元,或每股摊薄亏损0.20美元。
Business Progress:
业务进展:
Co-Diagnostics is progressing with the FDA review of its Co-Dx PCR platform for over-the-counter use.
The company is expanding international regulatory submissions and preparing for clinical evaluations in diverse markets like India and South Africa.
Engagement in global trade shows to promote the platform and readiness for manufacturing expansion in India for oligonucleotide synthesis.
Co-Diagnostics正在推进其Co-Dx PCR平台的FDA审查,以便进行非处方使用。
该公司正在扩大国际监管申报,并为印度和南非等多样市场的临床评估做准备。
参与全球交易会以推广平台,并准备在印度扩大制造业-半导体以进行寡核苷酸合成。
Opportunities:
机会:
Co-Diagnostics is targeting large unmet needs internationally with its innovative testing platforms for diseases like tuberculosis and HPV, particularly in markets like India, Africa, and South America.
The company sees potential in leveraging FDA clearance to streamline registrations across Latin American regions.
Co-Diagnostics 正在通过其创新检测平台来满足国际上对结核病和人乳头瘤病毒等疾病的巨大未满足需求,特别是在印度、非洲和南美等市场。
该公司看到利用FDA批准来简化拉丁美洲各地区注册的潜力。
Risks:
风险:
There's uncertainty in the FDA's remaining review timeline and decisions, impacting the commercial launch and adoption of the platform in the U.S.
The company faces challenges in aligning new test developments with varied international regulatory requirements.
FDA剩余审核时间表和决定的不确定性影响平台在美国的商业推出和采用。
该公司在将新测试开发与各种国际监管要求对齐方面面临挑战。
More details: Co-diagnostics IR
更多详情:Co-Diagnostics IR
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