Biopharma Transcript

Adagene Inc. ADAG

Nasdaq · Phase 2 · oncology · antibody · EDGAR · Updated Oct 24, 2026

Adagene Inc. (Nasdaq: ADAG) is an oncology drug developer. Its lead program, ADG126 (muzastotug), is in Phase 2 for MSS metastatic colorectal cancer (with anti-PD-1). Its next catalyst on record is ADG138: Initiate first-in-human Phase 1 study in China (Q4 2026).

Upcoming catalysts

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

Next further out: ADG138 — Initiate first-in-human Phase 1 study in China (Q4 2026). 1 catalyst on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
ADG126 (muzastotug)MSS metastatic CRC, combination with anti-PD-1antibodyPhase 2
ADG116solid tumors (anti-CTLA-4)antibodyPhase 1
ADG138HER2-expressing advanced solid tumorsantibodyPre-clinical
XB404 (Exelixis-partnered SAFEbody ADC)ROR1/2 tumorsantibodyPre-clinical

Recent results and decisions

  1. Sep 22, 2026
    n/a China NMPA cleared the IND for ADG138, a HER2xCD3 double-masked T-cell engager (ex-US regulator).China’s National Medical Products Administration (NMPA) has approved the company’s investigational new drug (IND) application for ADG138 Filing
  2. Apr 17, 2026
    positive AACR interim: triplet ORR 66.7% (4/6) vs 32.5% (13/40) for atezolizumab+bevacizumab control (HCC mRECIST); small n.Triple combination of muzastotug + atezolizumab + bevacizumab resulted in much higher overall response rates (ORR) compared to the atezolizumab + bevacizumab control arm (66.7% vs. 32.5%, respectively by Investigator per HCC-specific Modified RECIST v1.1) Filing
  3. Apr 1, 2026
    positive Recap of ASCO 2025 data: 29% (6/21) confirmed ORR at 20 mg/kg; mOS 19.4 months at 10 mg/kg; 4% discontinuation, no DLTs, no Grade 4/5 TRAEs across 67 patients.As presented at ASCO 2025, muzastotug showed 29% (6/21) confirmed overall response rate (ORR) in the combined 20 mg/kg dose cohorts. Filing

For subscribers

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