Curis to Report First Quarter 2025 Financial and Operating Results and Host Conference Call and Webcast on May 6, 2025
Rhea-AI Summary
Curis (NASDAQ: CRIS), a biotechnology company developing emavusertib (CA-4948), has scheduled its first quarter 2025 financial results announcement for May 6, 2025, at 8:00 a.m. ET.
The company will host a conference call and webcast at 8:30 a.m. ET on the same day. Investors can participate through:
- U.S. dial-in: (800)-836-8184
- International dial-in: (646)-357-8785
- Live audio webcast: Available on the Curis website's events & presentations section
Emavusertib, their key drug candidate, is an oral small molecule IRAK4 inhibitor. A replay of the conference call will be accessible at www.curis.com.
Positive
- Curis maintains its NASDAQ listing status (CRIS)
- Company continues development of emavusertib, a key IRAK4 inhibitor drug candidate
Negative
- No preliminary financial results provided ahead of the earnings call
- Focus on single drug candidate (emavusertib) suggests limited pipeline diversity
News Market Reaction 1 Alert
On the day this news was published, CRIS declined 2.69%, reflecting a moderate negative market reaction.
Data tracked by StockTitan Argus on the day of publication.
Participants may join by dialing (800)-836-8184 from the United States or (646)-357-8785 from other locations or a live audio webcast can be accessed here or from the events & presentations section of the Curis website. A replay of the conference call will be available at www.curis.com.
About Curis, Inc.
Curis is a biotechnology company focused on the development of emavusertib, an orally available, small molecule IRAK4 inhibitor. Emavusertib is currently being evaluated in the Phase 1/2 TakeAim Lymphoma study (CA-4948-101) in patients with relapsed/refractory primary central nervous system lymphoma (PCNSL) in combination with the BTK inhibitor ibrutinib, as a monotherapy in the Phase 1/2 TakeAim Leukemia study (CA-4948-102) in patients with relapsed/refractory acute myeloid leukemia (AML) and relapsed/refractory high risk myelodysplastic syndrome (hrMDS), and as a frontline combination therapy with venetoclax and azacitidine in patents with AML (CA-4948-104). Emavusertib has received Orphan Drug Designation from the
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SOURCE Curis, Inc.