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CervoMed Inc.
CRVO · Nasdaq · ·
下次财报：2026年11月6日
US$2.88+8.7%9月29日 收盘
- 1M
- +12.1%
- 6M
- -28.0%
- 1Y
- -64.1%
- 5Y
- -92.6%
CRVO · Nasdaq · ·
下次财报：2026年11月6日
US$2.88+8.7%9月29日 收盘
CervoMed Inc. 预定于 2026年11月6日发布下一份财报。日期来自 Nasdaq 财报日历，公司有时会调整。
截至 2026年6月30日 的季度，与去年同季度相比。
| 指标 | 截至该日的 3 个月2026年6月30日 | 截至该日的 3 个月2025年6月30日 | 变动 |
|---|---|---|---|
| 营业收入合计 | US$0.00 | US$1.8M | -100.00% |
| 利润 | -US$6.6M | -US$6.3M | -5.01% |
| 每股收益 | -US$0.55 | -US$0.05 | -905.48% |
| 自由现金流 | -US$2.3M | -US$1.4M | -62.04% |
这些是单季度数字，不是滚动一年——本站其他地方的数字覆盖十二个月，会大得多。季节性业务在两者之间摆动很大：ServiceNow 在十二月季度赚 20 亿美元自由现金流，在六月季度只有 5 亿。
对比对象是去年同一季度，而不是分析师预测。要说“超预期”或“不及预期”需要一致预期数据，那是我们没有的授权数据——而搞错它比不提更糟。
暂无 CervoMed Inc. 的业绩电话会文字记录。
“The second quarter was marked by meaningful progress across both our business and pipeline. The additional analyses presented at AAIC 2026 further strengthen our conviction in neflamapimod's potential as a meaningful, disease-modifying treatment for DLB. These findings provide important insight into the RewinD-LB results, reinforce the treatment effect observed in patients with pure DLB, and support selection of the 50 mg three-times-daily (TID) dose for our planned Phase 3 trial. Looking ahead, our primary strategic objective is securing a partner to support the advancement of neflamapimod into Phase 3 and realize its potential for patients living with DLB,”
逐字引自公告，且只在文件将其归于具名人士时才展示。
公告在收盘后或开盘前发布，因此这里的变动是随后的那个交易日。
CervoMed is a clinical-stage company developing treatments for age-related brain disorders. Its lead drug candidate, neflamapimod, is an oral small molecule targeting critical disease processes underlying degenerative disorders of the brain by inhibiting a key enzyme involved in neuroinflammation and neurodegeneration. CervoMed’s recently completed Phase 2b RewinD-LB trial evaluated neflamapimod in patients with DLB, enriched for those without AD co-pathology. In November 2025, CervoMed announced alignment with the FDA on a potential registration path for neflamapimod in DLB, and the Company is currently focused on identifying a strategic partner to advance neflamapimod into a Phase 3 trial in DLB. CervoMed also recently completed enrollment in its ongoing Phase 2a clinical trial evaluating neflamapimod in nfvPPA, a subtype of frontotemporal disorders, from which interim biomarker data is anticipated in the early fourth quarter of 2026, and expects the first patient to be dosed with neflamapimod in the EXPERTS-ALS Phase 2a clinical trial in the fourth quarter of 2026.
公司自己的描述，取自公告末尾。
引述和公司简介来自 CervoMed Inc. 于 2026年8月10日 提交的第 2.02 项 8-K 文件；表格根据其季度报告编制。 在 EDGAR 上阅读公告 股价已按拆股和分红复权。