A Dose-Escalation and Expansion Study of the Safety and Efficacy of XL092 in Combination With Immuno-Oncology Agents in Subjects With Unresectable Advanced or Metastatic Solid Tumors
Latest Information Update: 04 Apr 2024
At a glance
- Drugs Bempegaldesleukin (Primary) ; Ipilimumab (Primary) ; Nivolumab (Primary) ; Nivolumab/relatlimab (Primary) ; Relatlimab (Primary) ; Zanzalintinib (Primary)
- Indications Adenocarcinoma; Carcinoma; Colorectal cancer; Head and neck cancer; Liver cancer; Non-small cell lung cancer; Prostate cancer; Renal cell carcinoma; Solid tumours; Squamous cell cancer; Urogenital cancer
- Focus Adverse reactions; Therapeutic Use
- Acronyms STELLAR-002
- Sponsors Exelixis
- 07 Feb 2023 According to an Exelixis media release, Exelixis has established a recommended dose of 100 mg for zanzalintinib in combination with nivolumab, and we have begun enrolling expansion cohorts for patients with clear cell RCC, The novel triplet combination of zanzalintinib and the fixed-dose combination of nivolumab and relatlimab has the potential to be used in multiple expansion cohorts
- 18 Jan 2023 According to ClinicalTrials.gov record, one new treatment arm (Experimental: XL092 + Nivolumab + Relatlimab Dose-Escalation Cohorts) has been added into the study. Hence treatment arms has been changed from 6 to 7. and 4 new indication were added which includes Hepatocellular Carcinoma, Non-small Cell Lung Cancer, Colorectal Cancer, Head and Neck Squamous Cell Carcinoma.
- 18 Jan 2023 Planned number of patients changed from 826 to 1078.