| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 6.96M | 2.82M | 21.05M | 13.54M | 10.14M | 1.08M |
| Gross Profit | 6.25M | 2.82M | -67.10M | 8.40M | 6.81M | -19.49M |
| EBITDA | -130.55M | -119.74M | -80.10M | -59.91M | -45.30M | -25.00M |
| Net Income | -136.78M | -127.50M | -89.22M | -65.81M | -48.63M | -26.02M |
Balance Sheet | ||||||
| Total Assets | 298.56M | 371.12M | 272.15M | 199.09M | 188.11M | 49.74M |
| Cash, Cash Equivalents and Short-Term Investments | 218.04M | 290.11M | 192.04M | 120.03M | 161.41M | 34.79M |
| Total Debt | 64.40M | 97.38M | 92.43M | 85.98M | 6.04M | 7.43M |
| Total Liabilities | 121.85M | 130.15M | 121.28M | 99.66M | 27.33M | 92.20M |
| Stockholders Equity | 176.71M | 240.97M | 150.87M | 99.43M | 160.78M | -42.46M |
Cash Flow | ||||||
| Free Cash Flow | -131.25M | -114.65M | -64.50M | -70.73M | -58.62M | -7.26M |
| Operating Cash Flow | -126.18M | -110.82M | -61.36M | -66.50M | -48.68M | -3.02M |
| Investing Cash Flow | 6.91M | -52.61M | -60.76M | -4.22M | -9.94M | -4.24M |
| Financing Cash Flow | 46.51M | 208.76M | 135.44M | 29.36M | 189.67M | 288.00K |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
46 Neutral | $93.78M | -0.56 | -49.55% | ― | -33.76% | 17.10% | |
46 Neutral | $118.48M | -1.46 | -97.49% | ― | -100.00% | 62.82% | |
43 Neutral | $107.90M | -0.90 | -130.27% | ― | ― | 35.81% | |
41 Neutral | $65.83M | ― | -63.33% | ― | -42.94% | 12.25% | |
39 Underperform | $78.18M | -0.66 | -104.21% | ― | ― | 39.60% | |
34 Underperform | $104.23M | ― | -51.74% | ― | ― | 29.72% |
On November 3, 2025, TScan Therapeutics announced a strategic shift to prioritize its hematologic malignancies program, pausing enrollment in its solid tumor trial and focusing on preclinical efforts for solid tumors and autoimmunity target discovery. This decision, following a positive meeting with the FDA regarding the pivotal trial design for TSC-101, includes a 30% workforce reduction, aiming to save $45 million annually in 2026 and 2027, and extends the company’s cash runway into the second half of 2027.
The most recent analyst rating on (TCRX) stock is a Hold with a $2.00 price target. To see the full list of analyst forecasts on TScan Therapeutics stock, see the TCRX Stock Forecast page.
Study Overview: TScan Therapeutics, Inc. is conducting a Phase 1 basket study titled A Phase 1 Basket Study Evaluating the Safety and Feasibility of T-Plex, Autologous Customized T Cell Receptor-Engineered T Cells Targeting Multiple Peptide/HLA Antigens in Participants With Antigen-positive Locally Advanced (Unresectable) or Metastatic Solid Tumors. The study aims to assess the safety and feasibility of T-Plex therapies in treating various solid tumors, particularly those associated with HPV. This research is significant as it explores personalized cellular therapies, potentially offering new treatment avenues for patients with advanced cancers.
Study Overview: TScan Therapeutics, Inc. is conducting a long-term follow-up study titled A Long-term Follow-up Study to Assess Safety in Participants Who Received an Investigational T-Cell Receptor Engineered T-Cell (TCR-T) Product. The study aims to monitor the long-term safety and efficacy of TSC-100 and TSC-101 TCR-T therapies in participants who previously received treatment in the TSCAN-001 study. This research is significant as it seeks to provide insights into the prolonged effects and safety of these innovative therapies for conditions like AML, ALL, and MDS.
Study Overview: TScan Therapeutics, Inc. is conducting a screening study titled Screening Study to Determine HLA Type, HLA Loss of Heterozygosity Status and Tumor Antigen Expression in Participants With Locally Advanced (Unresectable) or Metastatic Solid Tumors. The study aims to collect samples for HLA genotyping, HLA Loss of Heterozygosity (LOH) assessment, and Tumor-associated Antigens (TAA) testing in patients with various metastatic solid tumors. The significance lies in determining eligibility for potential enrollment in further TScan clinical studies.
Study Overview: TScan Therapeutics, Inc. is conducting a clinical study titled A Controlled Multi-Arm Phase 1 Umbrella Study Evaluating the Safety and Feasibility of T-Cell Receptor Engineered Donor T-Cells Targeting HA1 (TSC-100) or HA2 (TSC-101) in HLA-A0201 Positive Patients Undergoing Allogeneic Peripheral Blood Stem Cell Transplantation. The study aims to assess the safety, feasibility, and preliminary efficacy of TSC-100 and TSC-101 in patients with acute myeloid leukemia (AML), myelodysplastic syndromes (MDS), or acute lymphoblastic leukemia (ALL) undergoing stem cell transplantation. This research is significant as it explores innovative treatments for these serious conditions.
On September 9, 2025, TScan Therapeutics released an updated corporate presentation outlining revised development and operational milestones, including adjusted timelines for its solid tumor program and updates on its pipeline for hematologic malignancies. The presentation, intended for investors and stakeholders, reflects the company’s ongoing efforts in target discovery initiatives in autoimmunity and highlights its strategic focus on advancing its TCR-T therapy candidates. This update is significant for stakeholders as it provides insights into TScan’s future growth strategies and its potential impact on the biotechnology industry.
The most recent analyst rating on (TCRX) stock is a Hold with a $1.50 price target. To see the full list of analyst forecasts on TScan Therapeutics stock, see the TCRX Stock Forecast page.
TScan Therapeutics, Inc. is a clinical-stage biotechnology company specializing in T cell receptor-engineered T cell therapies for cancer treatment, with a focus on hematologic malignancies and solid tumors. In its second quarter 2025 financial report, TScan Therapeutics highlighted significant advancements in its clinical programs, including the anticipated dosing of solid tumor patients with multiplex TCR-T therapies and the upcoming presentation of two-year relapse data from its ALLOHA Phase 1 trial. The company reported a substantial increase in revenue to $3.1 million, driven by its collaboration with Amgen, while research and development expenses rose to $32.6 million due to expanded manufacturing capabilities. Despite a net loss of $37 million, TScan maintains a strong cash position of $218 million, expected to fund operations into early 2027. Looking ahead, TScan aims to initiate a registrational trial for its lead candidate TSC-101 and file an IND for a new therapy, reflecting a strategic focus on advancing its pipeline and enhancing manufacturing efficiency.