| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 0.00 | 1.89M | 19.94M | 16.40M | 0.00 | 0.00 |
| Gross Profit | -832.00K | 71.00K | 18.18M | 13.89M | 0.00 | -777.00K |
| EBITDA | -66.69M | -64.05M | -32.47M | -51.30M | -49.87M | -14.26M |
| Net Income | -72.84M | -70.52M | -37.37M | -53.81M | -49.98M | -14.94M |
Balance Sheet | ||||||
| Total Assets | 79.63M | 126.93M | 174.83M | 160.25M | 179.25M | 96.40M |
| Cash, Cash Equivalents and Short-Term Investments | 65.71M | 111.00M | 134.34M | 129.31M | 157.53M | 92.57M |
| Total Debt | 37.30M | 37.09M | 51.92M | 14.68M | 15.66M | 2.54M |
| Total Liabilities | 50.01M | 53.54M | 63.46M | 37.91M | 26.46M | 7.18M |
| Stockholders Equity | 29.61M | 73.39M | 111.37M | 122.34M | 152.79M | 89.22M |
Cash Flow | ||||||
| Free Cash Flow | -63.64M | -56.44M | -33.38M | -44.21M | -43.37M | -19.18M |
| Operating Cash Flow | -63.52M | -56.19M | -32.61M | -40.60M | -42.88M | -18.62M |
| Investing Cash Flow | -123.00K | -254.00K | -769.00K | -3.61M | -498.00K | -560.00K |
| Financing Cash Flow | 6.21M | 13.08M | 58.43M | 15.91M | 109.43M | 93.86M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
66 Neutral | $307.14M | -2.41 | -172.70% | ― | ― | 5.51% | |
52 Neutral | $78.46M | -2.93 | -71.42% | ― | -38.81% | -76.96% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
45 Neutral | $32.06M | -0.41 | -122.43% | ― | -100.00% | -8.30% | |
45 Neutral | $72.24M | -1.04 | ― | ― | ― | -9.32% | |
28 Underperform | $160.35M | -1.30 | -63.45% | ― | ― | 63.31% |
On December 18, 2025, Werewolf Therapeutics reported a pipeline update and 2026 business priorities centered on its INDUKINE and INDUCER platforms, highlighting preliminary clinical data and a shift toward partnering for late‑stage development. The company showcased Phase 1/1b results for WTX‑124, an IL‑2 INDUKINE, showing objective and durable responses as monotherapy in melanoma, cutaneous squamous cell carcinoma, and gastroesophageal junction cancer and in combination with pembrolizumab across multiple solid tumors as of October 30, 2025, with a 21% objective response rate in heavily pretreated advanced cutaneous melanoma and 30% in patients who had previously responded to immunotherapy; the FDA has accepted 18 mg as the recommended Phase 2 dose and provided initial guidance for a monotherapy registration path in post‑ICI relapsed or refractory melanoma. Werewolf also detailed early Phase 1b/2 data for its IL‑12 INDUKINE WTX‑330 through October 31 and December 2, 2025, indicating improved safety, favorable pharmacokinetics versus recombinant IL‑12 and antitumor activity including a confirmed partial response in metastatic gall bladder cancer, supported by an optimized manufacturing process. Looking ahead, the company expects to complete the WTX‑124 Phase 1/1b trial and deliver further data in the first half of 2026 and to provide an update from the dose‑finding Part A of the WTX‑330 Phase 1b/2 trial over the same period, but it signaled that additional funding and strategic partnerships will be required to advance both programs into registration‑enabling or combination studies, affecting the pace and scope of future clinical development. In parallel, Werewolf is advancing its INDUCER T‑cell engager platform, reporting preclinical data on WTX‑1011 and the newly announced WTX‑2022 that showed strong tumor‑specific activation, antitumor activity in xenograft models, and low cytokine release in non‑human primates, with cell line development and IND‑enabling studies underway and planned investigational filings around mid‑2027, subject to financing, positioning the company to compete as a differentiated player in next‑generation T‑cell engager therapies.
Werewolf Therapeutics announced the passing of Dr. Alon Lazarus, a Board member, on September 30, 2025. His death left the company’s Audit Committee noncompliant with Nasdaq’s listing rules, prompting the company to plan for appointing a new independent director to regain compliance.