XNCR Xencor Inc

BULLISH Impact: 7/10 8-K
Horizon months Filed May 5, 2026 Processed 1mo ago SEC 0001326732-26-000036
8-K context-dependent: Items 7.01
Latest settled — T+20d
XNCR ▼ -12.76% at T+20d
LONG call ✗ call lost -12.76% · α vs SPY -17.72% · entry $12.85 → $11.21
Next anchor: T+60d in 6w
Last close $12.33 (close Jun 12) · -4.05% from $12.85 entry
Entry anchored
May 5, 06:26 AM ET
via Databento tick
T+1d
+1.25%
call +1.25% · α -0.14%
$13.01
settled 6w ago
T+5d
-0.47%
call -0.47% · α -2.45%
$12.79
settled 5w ago
T+20d
-12.76%
call -12.76% · α -17.72%
$11.21
settled 12d ago
T+60d
call — · α —
in 6w

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Executive Summary

Xencor reported final Phase 1 data for XmAb942, an anti-TL1A antibody for IBD, showing a terminal half-life of 74.1 days, favorable safety, and low immunogenicity (0% neutralizing antibodies at target dose). The company also presented preclinical data for XmAb412, a TL1A x IL23p19 bispecific, with predicted human half-life of 60-70 days. Enrollment in the Phase 2b XENITH-UC study remains on track with a blinded interim analysis expected around year-end 2026 and primary endpoint results in 2H27.

Actionable Insight

XmAb942 Phase 1 data supports best-in-class profile with 74-day half-life enabling Q12W SC dosing and low immunogenicity. The XENITH-UC Phase 2b blinded interim around YE26 is the next major catalyst. XmAb412 FIH start in 3Q26 adds pipeline optionality. Monitor for partnership interest given precedent valuations shown ($1.5B-$10B+).

Key Facts

  • XmAb942 Phase 1 estimated terminal half-life of 74.1 days from pooled single-dose cohorts
  • 0% neutralizing antibodies (NAb+) at XENITH-UC target dose regimen; 25% ADA+ at target dose
  • 86% of patients predicted to achieve >99% TL1A inhibition at induction (Week 12) per QSP model
  • 90% of patients predicted to achieve >90% TL1A inhibition at maintenance (Week 52) with Q12W SC dosing
  • No serious or severe TEAEs; TEAE rates similar between XmAb942 (75%) and placebo (69%)
  • XmAb412 predicted human half-life of 60-70 days; NHP half-life >20 days
  • XmAb412 FIH study expected to begin 3Q26
  • XENITH-UC Phase 2b enrolling ~220 patients; blinded interim analysis ~YE26, primary endpoint 2H27
  • Cash position ~$611M as of Dec 31, 2025

Financial Impact

No financial data reported; clinical-stage biotech with ~$611M cash position

Risk Factors

  • Phase 2b XENITH-UC results may not replicate Phase 1 PK/PD predictions
  • Competitive landscape includes multiple first-gen anti-TL1A programs (afimkibart, tulisokibart, duvakitug) in Phase 3
  • ADA incidence of 57% across all doses could impact long-term efficacy if neutralizing antibodies emerge
  • No revenue-generating products; dependent on pipeline success and partnerships

Market Snapshot

Exchange
Nasdaq
Sector
Pharmaceutical Preparations
Analyst Consensus
85% bullish (20 analysts)

Documents Analyzed

This report is based on 6 SEC documents filed with EDGAR.

DocumentAccession Number
8-K Filing (Primary)0001326732-26-000036
Document: xncr-20260504xexx992.htm0001326732-26-000036
Document: xncr-20260504.htm0001326732-26-000036
Document: 0001326732-26-000036-index-headers.html0001326732-26-000036
Document: 0001326732-26-000036-index.html0001326732-26-000036
Document: 0001326732-26-000036.txt0001326732-26-000036
6 reports for XNCR
Performance horizon
67% Hit rate 2 of 3 directional calls best @ T+1▲ +13.11%Feb 25, 2026
Filters
Rows
Reports for XNCR — sortable, filterable
Type Now
May 6, 2026
5w ago
8-K
BEARISH ★ 7/10
$12.31 $11.42▲ +7.23%▲ +10.37%$12.33 (−0.16%)
May 5, 2026
5w ago
8-K
BULLISH ★ 7/10
$12.85 $11.21▼ −12.76%▼ −17.72%$12.33 (−4.05%)
Apr 27, 2026
6w ago
8-K
NEUTRAL ★ 3/10
$12.15 $11.63▼ −4.28%▼ −9.75%$12.33 (+1.48%)
Mar 5, 2026
14w ago
Insider Cluster
NEUTRAL ★ 3/10
$11.16 $12.81▲ +14.78%▲ +18.57%$12.33 (+10.48%)
Mar 4, 2026
14w ago
8-K
BEARISH ★ 8/10
$11.16 $12.81▼ −14.78%▼ −18.57%$12.33 (−10.48%)
Feb 25, 2026
15w ago
8-K
BULLISH ★ 7/10
$11.98 $12.40▲ +3.51%▲ +8.74%$12.33 (+2.92%)
Showing 6 of 6

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