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

Author:

Subbiah Vivek1ORCID,Chawla Sant P.2ORCID,Conley Anthony P.3ORCID,Wilky Breelyn A.4ORCID,Tolcher Anthony5ORCID,Lakhani Nehal J.6ORCID,Berz David7ORCID,Andrianov Vasily8ORCID,Crago William8ORCID,Holcomb Monica8ORCID,Hussain Abrahim8ORCID,Veldstra Carson8ORCID,Kalabus James8ORCID,O’Neill Brianne8ORCID,Senne Lane8ORCID,Rowell Emily8ORCID,Heidt Analeah B.8ORCID,Willis Katelyn M.8ORCID,Eckelman Brendan P.8ORCID

Affiliation:

1. 1Department of Investigational Cancer Therapeutics, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas; Sarah Cannon Research Institute, Nashville, Tennessee.

2. 2Sarcoma Oncology Research Center, Santa Monica, California.

3. 3Department of Sarcoma Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.

4. 4Department of Medicine, Division of Medical Oncology, University of Colorado School of Medicine, Aurora, Colorado.

5. 5NEXT Oncology, San Antonio, Texas.

6. 6START Midwest, Michigan.

7. 7Valkyrie Clinical Trials, Los Angeles, California.

8. 8Inhibrx, Inc, La Jolla, California.

Abstract

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 I 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 I study of solid tumors, which 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 I 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 two 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 II trial (ChonDRAgon, NCT04950075) will further evaluate INBRX-109 in conventional chondrosarcoma.

Funder

not applicable

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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