Biopharma Transcript

Xencor Inc XNCR

Nasdaq · Phase 1 · oncology · antibody · EDGAR · Updated Nov 5, 2026

Xencor Inc (Nasdaq: XNCR) is an oncology drug developer. Its lead program, XmAb819 (ENPP3 x CD3), is in Phase 1 for Clear cell renal cell carcinoma (ccRCC).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Pipeline

ProgramIndicationModalityStage
XmAb942 (Xtend TL1A)Ulcerative colitis (UC)antibodyPhase 2
XmAb819 (ENPP3 x CD3)ccRCC and ENPP3+ tumorsantibodyPhase 1
XmAb541 (CLDN6 x CD3)High-grade serous ovarian cancer, germ cell tumorsantibodyPhase 1
XmAb808 (B7-H3 x CD28)CLDN6+ tumors (combination with XmAb541)antibodyPhase 1
XmAb412 (TL1A x IL-23p19)Autoimmune/inflammatory diseaseantibodyPhase 1
Plamotamab (CD20 x CD3)Rheumatoid arthritis (RA)antibodyPhase 1
XmAb657 (CD19 x CD3)Idiopathic inflammatory myopathies, systemic sclerosis, Sjögren's diseaseantibodyPhase 1

Recent results and decisions

  1. Oct 26, 2026
    positive XmAb819 Phase 1 dose expansion reported 45.5% confirmed objective response rate at 400 mcg/kg IV target dose in heavily pre-treated advanced ccRCC patients.400 mcg/kg chosen as proposed IV RP3D based on 45.5% cORR, 55% uORR and 82% 6-month PFS Kaplan-Meier estimate. Filing
  2. Oct 1, 2026
    positive XmAb819 achieved 45.5% confirmed objective response rate at 400 mcg/kg IV dose in advanced ccRCC patients.As of the October 1, 2026, data-cut, the efficacy-evaluable cohort at the 400 mcg/kg intravenous (IV) dose (n=11) reported five confirmed partial responses for a confirmed objective response rate of 45.5% per investigator assessment (RECIST v1.1). Filing
  3. Sep 1, 2026
    positive XmAb819 achieved 45% confirmed ORR and 82% disease control rate at 400 mcg/kg IV target dose in heavily pre-treated advanced ccRCC patients.400 mcg/kg chosen as proposed IV RP3D based on 45.5% cORR, 55% uORR and 82% 6-month PFS Kaplan-Meier estimate. Filing

6 more on record.

For subscribers

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