MARKET

ALLR

ALLR

Allarity
NASDAQ
0.9400
+0.1429
+17.93%
After Hours: 0.9348 -0.0052 -0.55% 19:57 04/17 EDT
OPEN
0.8000
PREV CLOSE
0.7971
HIGH
0.9500
LOW
0.7799
VOLUME
1.92M
TURNOVER
--
52 WEEK HIGH
103.80
52 WEEK LOW
0.6138
MARKET CAP
15.99M
P/E (TTM)
-0.0601
1D
5D
1M
3M
1Y
5Y
1D
Allarity Therapeutics Restructures Board of Directors
TipRanks · 3d ago
Weekly Report: what happened at ALLR last week (0407-0411)?
Weekly Report · 6d ago
Weekly Report: what happened at ALLR last week (0331-0404)?
Weekly Report · 04/07 10:20
US Stocks Likely To Open Mixed After Disappointing Q1 Performance: 'April Does Better After A Weak Q1,' Says Expert
Benzinga · 04/01 08:59
XPeng, Ultralife And 3 Stocks To Watch Heading Into Tuesday
Benzinga · 04/01 07:36
Based on the provided financial report articles, the title of the article is likely: "Annual Report (Form 10-K) for the fiscal year ended December 31, 2024 of Allarity Therapeutics, Inc." This title is inferred from the presence of the following information in the text: * The report is an annual report (Form 10-K) filed with the Securities and Exchange Commission (SEC). * The report covers the fiscal year ended December 31, 2024. * The company is Allarity Therapeutics, Inc.
Press release · 03/31 23:16
Allarity Therapeutics GAAP EPS of -$15.65
Seeking Alpha · 03/31 21:50
Allarity Therapeutics FY 2025 GAAP EPS $(15.65) Beats $(46.80) Estimate
Benzinga · 03/31 20:12
More
About ALLR
Allarity Therapeutics, Inc. is a clinical-stage biopharmaceutical company dedicated to developing personalized cancer treatments. It is focused on development of stenoparib, a PARP/tankyrase inhibitor for advanced ovarian cancer patients, using its DRP technology to develop a companion diagnostic that can be used to select those patients expected to derive clinical benefit from stenoparib. Its therapeutic candidate, stenoparib, is a dual inhibitor of the key DNA damage repair enzyme PARP, as well as Tankyrases, critical enzymes involved in the WNT signaling pathway commonly activated in many cancers. Inhibition of key DNA damage repair enzymes, such as PARP, has clinically demonstrated to be therapeutically beneficial in the treatment of cancers (ovarian cancers). The DRP method builds on the comparison of sensitive vs. resistant human cancer cell lines, including transcriptomic information from cell lines, combined with clinical tumor biology filters and prior clinical trial outcomes.

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