Biopharma Transcript

Coherus Oncology, Inc. CHRS

Nasdaq · Phase 2 · oncology · antibody · EDGAR · Updated Nov 4, 2026

Coherus Oncology, Inc. (Nasdaq: CHRS) is an oncology drug developer. Its lead program, LOQTORZI (toripalimab-tpzi), is in Phase 2 for Nasopharyngeal carcinoma (1L with cisplatin/gemcitabine; monotherapy after platinum).

Upcoming catalysts

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

Pipeline

ProgramIndicationModalityStage
LOQTORZI (toripalimab-tpzi), anti-PD-1Nasopharyngeal carcinoma (FDA approved Oct 2023; US launch Jan 2024)antibodyApproved
casdozokitug (CHS-388), anti-IL-271L hepatocellular carcinoma, with toripalimab and bevacizumabantibodyPhase 2
tagmokitug (CHS-114), anti-CCR8HNSCC, upper GI adenocarcinoma, ESCC, colorectal cancer (Phase 1b/2a)antibodyPhase 1

Recent results and decisions

  1. Oct 28, 2026
    positive Tagmokitug plus toripalimab and chemotherapy achieved 75% confirmed ORR overall and 100% in PD-L1-positive first-line ESCC patients in Phase 1b TREGCHECK 102 Cohort C.In evaluable front-line esophageal squamous cell carcinoma (ESCC) patients, tagmokitug in combination with toripalimab and chemotherapy demonstrated a confirmed overall response rate (cORR) of 75% irrespective of PD-L1 status, and a cORR of 100% in PD-L1 positive patients as of October 14, 2026. Filing
  2. Oct 14, 2026
    positive Tagmokitug combination achieved 75% confirmed ORR (100% in PD-L1 positive patients) in first-line ESCC, updated to 89% cORR post-data-cutoff.In evaluable front-line esophageal squamous cell carcinoma (ESCC) patients, tagmokitug in combination with toripalimab and chemotherapy demonstrated a confirmed overall response rate (cORR) of 75% irrespective of PD-L1 status, and a cORR of 100% in PD-L1 positive patients as of October 14, 2026. Filing
  3. May 11, 2026
    completed enrollment Enrollment completed in the randomized Phase 2 trial of casdozokitug/toripalimab/bevacizumab in 1L uHCC.Enrollment is complete in the randomized Phase 2 trial of casdozokitug/toripalimab/bevacizumab in 1L uHCC and the first data readout is expected in mid-2026. Filing

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