1. Academic Validation
  2. Preclinical Characterization and Phase 1 Trial Results of INBRX-109, a Third-Generation, Recombinant, Humanized, Death Receptor 5 Agonist Antibody, in Chondrosarcoma

Preclinical Characterization and Phase 1 Trial Results of INBRX-109, a Third-Generation, Recombinant, Humanized, Death Receptor 5 Agonist Antibody, in Chondrosarcoma

  • Clin Cancer Res. 2023 Jun 2;CCR-23-0974. doi: 10.1158/1078-0432.CCR-23-0974.
Vivek Subbiah 1 Sant P Chawla 2 Anthony P Conley 3 Breelyn A Wilky 4 Anthony Tolcher 5 Nehal J Lakhani 6 David Berz 7 Vasily Andrianov 8 William Crago 8 Monica Holcomb 8 Abrahim Hussain 8 Carson Veldstra 8 James Kalabus 9 Brianne O'Neill 8 Lane Senne 10 Emily Rowell 8 Analeah B Heidt 8 Katelyn M Willis 11 Brendan P Eckelman 12
Affiliations

Affiliations

  • 1 Sarah Cannon, Nashville, TN, United States.
  • 2 Sarcoma Oncology Center, Santa Monica, California, United States.
  • 3 The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.
  • 4 University of Colorado School of Medicine, Aurora, CO, United States.
  • 5 South Texas Accelerated Research Therapeutics, San Antonio, TX, United States.
  • 6 START Midwest, Grand Rapids, Michigan, United States.
  • 7 Valkyrie Clinical Trials, United States.
  • 8 Inhibrx, Inc, United States.
  • 9 Inhibrx, Inc, San Diego, United States.
  • 10 Inhibrx, Inc, La Jolla, United States.
  • 11 Inhibrx, Inc, La Jolla, CA, United States.
  • 12 Inhibrix, San Diego, CA, United States.
Abstract

Purpose: Patients with unresectable/metastatic chondrosarcoma have poor prognoses; conventional chondrosarcoma is associated with a median progression-free survival (PFS) of <4 months after first-line chemotherapy. No standard targeted therapies are available. We present the preclinical characterization of INBRX-109, a third-generation Death Receptor 5 (DR5) agonist, and clinical findings from a phase 1 trial of INBRX-109 in unresectable/metastatic chondrosarcoma (NCT03715933).

Patients and methods: INBRX-109 was first characterized preclinically as a DR5 agonist, with binding specificity and hepatotoxicity evaluated in vitro and antitumor activity evaluated both in vitro and in vivo. INBRX-109 (3 mg/kg every 3 weeks) was then evaluated in a phase 1 study of solid tumors that included a cohort with any subtype of chondrosarcoma and a cohort with IDH1/IDH2-mutant conventional chondrosarcoma. The primary endpoint was safety. Efficacy was an exploratory endpoint, with measures including objective response, disease control rate, and PFS.

Results: In preclinical studies, INBRX-109 led to antitumor activity in vitro and in patient-derived xenograft models, with minimal hepatotoxicity. In the phase 1 study, INBRX-109 was well tolerated and demonstrated antitumor activity in unresectable/metastatic chondrosarcoma. INBRX-109 led to a disease control rate of 87.1% (27/31; durable clinical benefit, 40.7% [11/27]), including 2 partial responses, and median PFS of 7.6 months. Most treatment-related adverse events, including liver-related events, were low grade (grade ≥3 events in chondrosarcoma cohorts, 5.7%).

Conclusions: INBRX-109 demonstrated encouraging antitumor activity with a favorable safety profile in patients with unresectable/metastatic chondrosarcoma. A randomized, placebo-controlled, phase 2 trial (ChonDRAgon, NCT04950075) will further evaluate INBRX-109 in conventional chondrosarcoma.

Figures
Products