Valuation: Allarity Therapeutics, Inc.

Market Cap 2.04Cr 1.79Cr 1.66Cr 1.53Cr 2.87Cr 197.23Cr 2.92Cr 20Cr 7.76Cr 96Cr 7.65Cr 7.48Cr 333.74Cr P/E 2026 *
-1.39x
P/E 2027 * -1.32x
Enterprise Value 2.04Cr 1.79Cr 1.66Cr 1.53Cr 2.87Cr 197.23Cr 2.92Cr 20Cr 7.76Cr 96Cr 7.65Cr 7.48Cr 333.74Cr EV / Sales 2026 *
815x
EV / Sales 2027 * -
Free-Float
79.71%
Yield 2026 *
-
Yield 2027 * -
Manager TitleAgeSince
Chief Executive Officer 47 08/12/2023
Chief Tech/Sci/R&D Officer 65 01/07/2021
Director of Finance/CFO 48 01/07/2025
Director TitleAgeSince
Director/Board Member 47 07/07/2022
Chairman 58 19/01/2023
Director/Board Member 60 01/01/2023
Change 5-day change 1-year change 3-year change Capi.($)
-26.54%-10.92% - - 2.04Cr
+1.23%-3.08%+53.96%+87.98% 5.53TCr
+5.09%+6.24%+63.15%+66.42% 5.42TCr
+0.49%-0.47%+3.40%+422.75% 2.31TCr
-0.14%+0.11%-20.02%-14.36% 2.32TCr
+1.03%-0.76%+40.14%-3.59% 2.03TCr
-0.37%+0.71%+31.36%-29.32% 1.79TCr
+0.87%-2.80%+37.96%+600.00% 1.58TCr
-2.54%-12.88%+168.62%+289.45% 1.5TCr
+0.95%-0.61%+21.89%+178.23% 1.38TCr
Average -1.99%-0.37%+44.50%+177.51% 2.65TCr
Weighted average by Cap. +1.48%+1.19%+45.37%+140.67%

Financials

2026 *2027 *
Net sales 25T 21.99T 20.43T 18.79T 35.23T 24.21L 35.86T 2L 95.27T 11.81L 93.86T 91.82T 40.97L -
Net income -1.49Cr -1.31Cr -1.21Cr -1.12Cr -2.09Cr -143.93Cr -2.13Cr -15Cr -5.66Cr -70Cr -5.58Cr -5.46Cr -243.55Cr -1.61Cr -1.42Cr -1.32Cr -1.21Cr -2.28Cr -156.4Cr -2.32Cr -16Cr -6.15Cr -76Cr -6.06Cr -5.93Cr -264.65Cr
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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