EPS Reference Time Actual Consensus Previous
2026-05-13 FY2026Q1 PM -0.66 -0.66
2026-02-25 FY2025Q4 PM -0.09 -0.6 -0.62
2025-11-05 FY2025Q3 PM -0.08 -0.69 -0.71
2025-08-06 FY2025Q2 PM -0.41 -0.65 -1.07
2025-05-07 FY2025Q1 PM -0.66 -0.80 -1.11



Peers Price Chg Day Year Date
AbbVie 208.84 -6.14 -2.86% 3.57% Apr/02
Alnylam Pharmaceuticals 318.85 -9.88 -3.01% 21.62% Apr/02
Amgen 347.94 -5.34 -1.51% 12.29% Apr/02
Arrowhead Research 61.03 -1.89 -3.00% 406.05% Apr/02
AstraZeneca 15,316.00 294.00 1.96% 34.45% Apr/02
Biogen 177.34 -6.44 -3.50% 35.67% Apr/02
Bristol-Myers Squibb 59.60 -2.13 -3.45% 3.08% Apr/02
Cytokinetics 66.73 0.12 0.18% 64.68% Apr/02
GlaxoSmithKline 2,144.00 37.00 1.76% 46.30% Apr/02
J&J 243.04 -1.08 -0.44% 52.07% Apr/02

Indexes Price Day Year Date
USND 21879 38.23 0.18% 32.20% Apr/02
US2000 2530 17.67 0.70% 32.42% Apr/02

Xencor traded at $12.81 this Thursday April 2nd, increasing $0.28 or 2.23 percent since the previous trading session. Looking back, over the last four weeks, Xencor gained 6.57 percent. Over the last 12 months, its price rose by 43.61 percent. Looking ahead, we forecast Xencor to be priced at 12.42 by the end of this quarter and at 11.34 in one year, according to Trading Economics global macro models projections and analysts expectations.

Xencor, Inc. is a clinical-stage biopharmaceutical company that is focused on discovering and developing engineered monoclonal antibody and cytokine therapeutics to treat patients with cancer and autoimmune diseases. The Company uses its engineering capabilities to enable its understanding of protein structure and interactions to design XmAb technologies and develop candidates with properties. Its antibody design is focused on the segment of antibodies that interact with target antigens. It is focused on the Fc domain, which is the part of an antibody that interacts with various segments of the immune system and controls antibody structure. The Fc domain is constant and interchangeable among antibodies, and its engineered Fc domains are the XmAb technology, which can be readily substituted for natural Fc domains. Its drug candidates include Plamotamab, XmAb717, Vibecotamab, Tidutamab, XmAb841, XmAb104, XmAb306, XmAb104, XmAb564 and XmAb698.