Valuation: Allarity Therapeutics, Inc.

Market Cap 18.93M 16.55M 15.27M 14.07M 26.53M 1.82B 27.12M 182M 71.78M 893M 71.11M 69.55M 3.07B P/E 2026 *
-1.29x
P/E 2027 * -1.23x
Enterprise Value 18.93M 16.55M 15.27M 14.07M 26.53M 1.82B 27.12M 182M 71.78M 893M 71.11M 69.55M 3.07B EV / Sales 2026 *
757x
EV / Sales 2027 * -
Free-Float
79.71%
Yield 2026 *
-
Yield 2027 * -
Manager TitleAgeSince
Chief Executive Officer 47 07/12/2023
Chief Tech/Sci/R&D Officer 65 30/06/2021
Director of Finance/CFO 48 30/06/2025
Director TitleAgeSince
Director/Board Member 47 06/07/2022
Chairman 58 18/01/2023
Director/Board Member 60 31/12/2022
Change 5-day change 1-year change 3-year change Capi.($)
-26.54%-10.92% - - 18.93M
-0.56%-1.58%+54.78%+56.14% 53.83B
-7.17%-4.39%+42.72%+73.70% 52.1B
+0.80%-6.31%+5.62%+413.12% 23.48B
-0.09%-0.01%-16.85%-16.17% 23.13B
+3.35%+2.25%+36.29%-5.66% 19.36B
+0.07%-1.81%+34.32%-32.50% 17.56B
-5.16%-7.00%+168.44%+291.24% 15.2B
+3.52%-0.10%+33.34%+643.17% 14.83B
+0.43%-1.03%+25.75%+186.18% 14.06B
Average -3.15%-2.62%+42.71%+178.80% 25.95B
Weighted average by Cap. -1.48%-2.36%+41.27%+137.40%

Financials

2026 *2027 *
Net sales 25K 21.85K 20.16K 18.58K 35.02K 2.41M 35.8K 241K 94.78K 1.18M 93.89K 91.83K 4.06M -
Net income -14.86M -12.99M -11.98M -11.05M -20.82M -1.43B -21.28M -143M -56.34M -701M -55.81M -54.59M -2.41B -16.15M -14.11M -13.02M -12M -22.63M -1.56B -23.13M -156M -61.23M -762M -60.65M -59.32M -2.62B
Net Debt - -
Logo Allarity Therapeutics, Inc.
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.
Employees
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