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Xencor/$XNCR

1D1W1M3M6MYTD1Y5YMAX

About Xencor

Xencor Inc is a clinical-stage biopharmaceutical company focused on discovering and developing engineered antibody therapeutics to treat patients with cancer and autoimmune diseases. The company uses its XmAb technology platform to create antibody product candidates. Its pipeline includes XmAb819, XmAb541, XmAb808, XmAb942, Plamotamab and XmAb657. The group earns its revenue from collaboration agreements and licensing agreements and operates as a single reportable segment focused on discovering and developing engineered antibody therapeutics to treat patients with cancer and autoimmune diseases who have unmet medical needs.
Ticker
$XNCR
Sector
Health
Primary listing
NASDAQ
Employees
260

Xencor Metrics

BasicAdvanced
$2.2B
-
-$2.18
0.84
-

What the Analysts think about Xencor

Analyst ratings (Buy, Hold, Sell) for Xencor stock.
Analyst projections of the future price of Xencor stock.

Bulls say / Bears say

At the proposed dose, XmAb819 produced a 45.5% confirmed response rate in advanced kidney cancer, with an estimated 82% of patients progression-free at six months. The responses came in heavily pre-treated patients, making the early signal encouraging. (BusinessWire)
Xencor has selected a dose for further development and plans a global randomised study of XmAb819 against tivozanib, with FDA discussions on a possible accelerated-approval route due in the first half of 2027. This gives the programme a defined path towards testing whether the early results can translate into approval. (BusinessWire)
Xencor has other potential catalysts beyond XmAb819: its ulcerative-colitis drug XmAb942 is in Phase 2b, with an interim analysis expected around year-end 2026, while partner Zenas filed for approval of obexelimab and triggered a $10 million milestone. This gives investors clinical and partner-led sources of potential progress. (Xencor)
The 45.5% response rate for XmAb819 is based on just 11 patients at the selected dose, with no randomised comparison and only six months of median follow-up. The small sample leaves substantial uncertainty about how well the result will hold up in a larger trial. (Seeking Alpha, BusinessWire)
XmAb819 also carries a significant safety burden: 72.1% of patients in its combined expansion cohorts had a related Grade 3 or worse adverse event, commonly liver-enzyme elevations or rash. These effects could complicate treatment and development even though few patients stopped treatment because of them. (BusinessWire)
XmAb541 has shown modest response rates so far: about 14% in ovarian cancer and 28% in germ-cell tumours. Attempts to increase exposure were limited by reversible hearing impairment, which may restrict the drug’s effectiveness and dose range. (Xencor, ApexOnco)
Data summarised monthly by Lightyear AI. Last updated on 26 Oct 2026.

Xencor Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

Xencor Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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