Valuation: Allarity Therapeutics, Inc.

Market Cap 17.98M 15.73M 14.5M 13.44M 25.51M 1.71B 25.92M 174M 67.61M 842M 67.5M 66.04M 2.91B P/E 2026 *
-1.23x
P/E 2027 * -1.16x
Enterprise Value 17.98M 15.73M 14.5M 13.44M 25.51M 1.71B 25.92M 174M 67.61M 842M 67.5M 66.04M 2.91B EV / Sales 2026 *
719x
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% - - 17.98M
-0.71%+1.64%+73.80%+129.41% 57.72B
-3.80%-6.24%+67.04%+86.36% 52.65B
+1.17%+5.83%+16.39%+468.18% 24.46B
+0.38%+1.33%-14.32%-11.76% 23.84B
-3.05%+3.06%+42.36%-5.66% 19.28B
-0.38%+5.04%+44.15%-26.66% 17.8B
+3.46%+17.72%+206.66%+364.07% 17.29B
-6.73%+9.90%+36.04% - 15.28B
+2.79%+4.91%+29.26%+195.60% 14.35B
Average -3.34%+5.15%+55.71%+149.94% 26.96B
Weighted average by Cap. -1.12%+2.58%+57.67%+139.42%

Financials

2026 *2027 *
Net sales 25K 21.88K 20.16K 18.69K 35.48K 2.37M 36.05K 242K 94.02K 1.17M 93.86K 91.82K 4.05M -
Net income -14.86M -13.01M -11.99M -11.11M -21.09M -1.41B -21.43M -144M -55.89M -696M -55.8M -54.59M -2.41B -16.15M -14.13M -13.02M -12.07M -22.92M -1.53B -23.29M -156M -60.74M -756M -60.63M -59.32M -2.61B
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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