| Breakdown | TTM | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| Gross Profit | -1.08M | 0.00 | -3.64M | -6.33M | -7.01M | -8.89M |
| EBITDA | -8.09M | 0.00 | -7.38M | -10.64M | -11.39M | -13.44M |
| Net Income | -7.95M | -8.70M | -7.15M | -10.83M | -11.48M | -13.29M |
Balance Sheet | ||||||
| Total Assets | 11.51M | 21.49M | 5.74M | 9.36M | 12.81M | 25.17M |
| Cash, Cash Equivalents and Short-Term Investments | 10.71M | 21.03M | 5.38M | 8.49M | 11.78M | 24.06M |
| Total Debt | 0.00 | 0.00 | 0.00 | 35.00K | 170.00K | 295.00K |
| Total Liabilities | 1.67M | 1.34M | 1.01M | 1.63M | 1.97M | 3.24M |
| Stockholders Equity | 9.84M | 20.15M | 4.72M | 7.73M | 10.84M | 21.93M |
Cash Flow | ||||||
| Free Cash Flow | -7.28M | -8.71M | -7.11M | -10.75M | -12.25M | -11.91M |
| Operating Cash Flow | -7.27M | -8.70M | -7.11M | -10.75M | -12.13M | -11.86M |
| Investing Cash Flow | -4.00K | -12.00K | 8.00K | -5.00K | -121.00K | -51.00K |
| Financing Cash Flow | 12.59M | 23.64M | 4.00M | 7.41M | -26.00K | 21.72M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
53 Neutral | $12.59M | -0.72 | -107.58% | ― | ― | 83.95% | |
53 Neutral | $91.20M | -5.32 | -70.22% | ― | 185.71% | 79.03% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
44 Neutral | $4.55M | -1.09 | -207.73% | ― | 1.70% | -111.67% | |
43 Neutral | $6.86M | 0.64 | ― | ― | -29.78% | 88.96% | |
39 Underperform | $468.55K | ― | ― | ― | ― | 99.09% |
On February 17, 2026, Phio Pharmaceuticals Corp. amended the employment agreement of its President and CEO, Robert J. Bitterman, revising key severance and incentive terms. The change increases his severance to 12 months of base salary if he is terminated without cause or resigns for good reason, aligning his protection with typical biotech executive packages.
The amendment also raises Bitterman’s annual target bonus opportunity to 50% of his base salary from the prior 40% level. The move signals the board’s effort to strengthen executive retention and incentive alignment as the company navigates its ongoing strategic and operational priorities.
The most recent analyst rating on (PHIO) stock is a Buy with a $14.00 price target. To see the full list of analyst forecasts on Phio Pharmaceuticals stock, see the PHIO Stock Forecast page.
On February 10, 2026, Phio Pharmaceuticals reported that an independent Safety Monitoring Committee completed its review of the Phase 1b trial of PH-762 in skin cancers with a positive safety conclusion, finding no serious adverse events or dose-limiting toxicities among 22 patients across five dose-escalation cohorts. The company said the highest dose cohort showed an 85% pathological response rate, with four of six responders achieving complete tumor clearance, supporting continued evaluation of this dose in subsequent studies.
Updated efficacy data from the trial showed a 65% overall response rate in cutaneous squamous cell carcinoma, with 13 of 20 patients classified as pathologic responders and no cases of disease progression reported among any participants. Phio also noted that chemistry, manufacturing and controls work is progressing, with active pharmaceutical ingredient material expected in March 2026 to enable a non-human primate study and plans to begin cGMP manufacturing in the second half of 2026, marking a key step toward potential pivotal trials and reinforcing its development trajectory in immuno-oncology.
The most recent analyst rating on (PHIO) stock is a Hold with a $1.00 price target. To see the full list of analyst forecasts on Phio Pharmaceuticals stock, see the PHIO Stock Forecast page.
On January 20, 2026, Phio Pharmaceuticals reported pathology and safety data from all five cohorts in its Phase 1b intratumoral PH-762 dose-escalation trial in cutaneous carcinomas, showing favorable safety and tolerability across a 20-fold dose range with no dose-limiting toxicities or clinically relevant treatment-emergent adverse effects. Among 20 patients with cSCC, 14 were pathologic responders, including 10 with complete responses (100% clearance), two with major responses (over 90% clearance) and two with partial responses (over 50% clearance), contributing to a 70% overall response rate for squamous cell carcinomas, while one patient with metastatic Merkel cell carcinoma achieved a partial response and no patients experienced disease progression, positioning PH-762 as a promising non-surgical candidate in skin cancer treatment and informing the design of follow-on clinical trials.
The most recent analyst rating on (PHIO) stock is a Hold with a $1.00 price target. To see the full list of analyst forecasts on Phio Pharmaceuticals stock, see the PHIO Stock Forecast page.
On December 23, 2025, Phio Pharmaceuticals announced that the U.S. Food and Drug Administration had accepted the nonclinical protocol study design for PH-762, allowing the company to begin an FDA-required toxicology study in the first quarter of 2026 ahead of a potential pivotal human trial. The company is simultaneously working to secure commercially viable PH-762 drug product that meets current Good Manufacturing Practices in 2026, funded in part by recent financing, and reported encouraging interim data from its ongoing Phase 1b dose-escalation trial in skin cancer patients, with multiple complete and partial responses, no clinical disease progression, and no dose-limiting toxicities observed to date, underscoring both the clinical potential of PH-762 and a meaningful de-risking step in its development pathway.
The most recent analyst rating on (PHIO) stock is a Buy with a $14.00 price target. To see the full list of analyst forecasts on Phio Pharmaceuticals stock, see the PHIO Stock Forecast page.