| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 146.36M | 110.49M | 168.34M | 164.58M | 275.11M | 122.69M |
| Gross Profit | 89.96M | 110.49M | -85.26M | 155.78M | 267.62M | -47.11M |
| EBITDA | -72.79M | -186.17M | -125.87M | -72.16M | 51.26M | -71.00M |
| Net Income | -138.75M | -232.62M | -126.09M | -55.18M | 82.63M | -63.54M |
Balance Sheet | ||||||
| Total Assets | 868.81M | 951.95M | 952.69M | 846.27M | 838.21M | 703.24M |
| Cash, Cash Equivalents and Short-Term Investments | 386.78M | 497.77M | 593.73M | 623.06M | 334.11M | 603.00M |
| Total Debt | 69.27M | 231.95M | 83.43M | 59.63M | 33.97M | 11.63M |
| Total Liabilities | 243.50M | 277.92M | 283.56M | 118.77M | 104.71M | 130.80M |
| Stockholders Equity | 625.32M | 677.61M | 668.80M | 727.50M | 733.50M | 572.44M |
Cash Flow | ||||||
| Free Cash Flow | -143.67M | -208.28M | 63.86M | -18.92M | -32.83M | -18.77M |
| Operating Cash Flow | -138.98M | -202.19M | 85.11M | 24.48M | -16.85M | -5.00M |
| Investing Cash Flow | 126.06M | -7.87M | -111.06M | -119.72M | -46.25M | 100.19M |
| Financing Cash Flow | 12.08M | 197.15M | 26.18M | 5.70M | 43.04M | 18.04M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
59 Neutral | $1.30B | 34.05 | 15.02% | ― | 1128.17% | ― | |
55 Neutral | $1.32B | -10.20 | -28.57% | ― | -42.64% | -39.78% | |
54 Neutral | $1.02B | -7.88 | -19.61% | ― | 38.16% | 48.43% | |
54 Neutral | $1.18B | -3.52 | -46.24% | ― | -76.27% | 22.77% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
48 Neutral | $368.61M | ― | -52.18% | ― | 187.52% | 26.32% | |
46 Neutral | $732.89M | ― | -55.41% | ― | -22.52% | -37.00% |
Study Overview: Xencor Inc. is conducting a Phase 1 clinical study titled ‘A Phase 1, First-in-Human, Dose Escalation and Expansion Study to Evaluate the Safety and Tolerability of XmAb541 in Advanced Solid Tumors.’ The study aims to assess the safety and tolerability of XmAb541, an investigational drug, and to determine an optimal dose for future research. This study is significant as it explores potential treatment options for various advanced solid tumors, including ovarian and endometrial cancers.
Study Overview: Xencor Inc. is conducting a Phase 1 clinical study titled ‘A Phase 1 Multiple Dose Study to Evaluate the Safety and Tolerability of XmAb819 in Subjects With Relapsed or Refractory Clear Cell Renal Cell Carcinoma.’ The study aims to assess the safety and tolerability of XmAb®819, a treatment for patients with relapsed or refractory clear cell renal cell carcinoma, and to determine the minimum safe and biologically active dose.
Study Overview: Xencor Inc. is conducting a Phase 1b/2 study titled A Phase 1b/2, Open-label, Randomized Study of Vudalimab in Combination With Chemotherapy or Pembrolizumab in Combination With Chemotherapy as First-line Treatment in Patients With Advanced Non-small Cell Lung Cancer. The study aims to determine the optimal dose of vudalimab combined with chemotherapy and to assess its efficacy and safety compared to pembrolizumab plus chemotherapy in treating nonsquamous non-small cell lung cancer (NSCLC).
Study Overview: Xencor Inc. is conducting a clinical study titled A Phase 1, Randomized, Double-Blind, Placebo-Controlled Study in Healthy Participants Followed by a Randomized, Double-Blind, Placebo-Controlled Phase 2 Study in Participants With Moderate-To-Severe Active Ulcerative Colitis. The study aims to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of XmAb942 in healthy volunteers and its efficacy in participants with ulcerative colitis. This study is significant as it explores potential new treatments for ulcerative colitis, a chronic inflammatory bowel disease.
On October 24, 2025, Xencor, Inc. held a conference call to discuss initial results from its ongoing Phase 1 dose-escalation study of XmAb819, a bispecific T-cell engager for advanced clear cell renal cell carcinoma. The company also shared early data from the Phase 1 study of XmAb541 for ovarian cancer and germ cell tumors. These developments highlight Xencor’s continued progress in its oncology pipeline, potentially enhancing its competitive position in the market by advancing novel therapeutic candidates.
The most recent analyst rating on (XNCR) stock is a Buy with a $27.00 price target. To see the full list of analyst forecasts on Xencor stock, see the XNCR Stock Forecast page.
Study Overview: Xencor Inc. recently completed a Phase 1 clinical study titled ‘A Phase 1, First-in-Human, Dose-Finding and Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Activity of XmAb®808 in Combination With Pembrolizumab in Selected Advanced Solid Tumors.’ The study aimed to assess the safety and effectiveness of XmAb808, a novel therapeutic antibody, when used with pembrolizumab in treating advanced solid tumors. This research is significant as it explores new treatment avenues for challenging cancer types.
Study Overview: Xencor Inc. is conducting a Phase 1 clinical trial titled ‘A Phase 1, First-in-Human, Dose Escalation and Expansion Study to Evaluate the Safety and Tolerability of XmAb541 in Advanced Solid Tumors.’ The study aims to assess the safety and tolerability of XmAb541, an investigational drug, and determine the optimal dose for further research. This study is significant as it explores potential new treatments for advanced solid tumors.
Xencor, Inc. is a clinical-stage biopharmaceutical company specializing in engineered antibody therapeutics for cancer and autoimmune diseases, leveraging its protein engineering capabilities to develop XmAb drug candidates.
In a recent update, Xencor Inc. has completed a Phase 1 clinical study titled ‘A Phase 1, First-in-Human, Dose Escalation and Expansion Study to Evaluate the Safety and Tolerability of XmAb541 in Advanced Solid Tumors.’ The study aimed to assess the safety and tolerability of XmAb541, a monoclonal bispecific antibody, and to determine optimal dosing for future research. This investigational drug is intended to improve outcomes in patients with advanced solid tumors.
On July 31, 2025, Xencor announced the appointment of Raymond J. Deshaies, Ph.D., to its board of directors. Dr. Deshaies, a renowned biochemist and cell biologist with extensive experience in biotechnology and drug development, previously served as senior vice president of global research at Amgen Inc. His appointment is expected to bolster Xencor’s efforts in advancing its pipeline of XmAb drug candidates through clinical development, leveraging his deep understanding of biological mechanisms and track record of translating scientific insights into transformative medicines.
The most recent analyst rating on (XNCR) stock is a Buy with a $38.00 price target. To see the full list of analyst forecasts on Xencor stock, see the XNCR Stock Forecast page.
Study Overview: Xencor Inc. is conducting a Phase 1 study titled ‘A Phase 1 Multiple Dose Study to Evaluate the Safety and Tolerability of XmAb819 in Subjects With Relapsed or Refractory Clear Cell Renal Cell Carcinoma.’ The study aims to assess the safety and tolerability of XmAb819, a monoclonal bispecific antibody, in patients with advanced renal cell carcinoma, and to determine the minimum safe and biologically active dose.