A Phase 1 interventional study of Bardoxolone methyl in Advanced Solid Tumors and Lymphoid Malignancies, sponsored by Biogen. Completed at 3 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-05-28.
Sponsored by Biogen · Phase 1, Interventional, and Treatment
This study assesses the tolerability, safety, efficacy and pharmacokinetics of Bardoxolone methyl (RTA 402) in advanced solid tumors and lymphoid malignancies.
Bardoxolone methyl (RTA 402) is a synthetic triterpenoid that has demonstrated significant in vivo single agent anti-cancer activity. This is an open-label phase I dose-escalation study of Bardoxolone methyl (RTA 402) administered orally for the first 21 days of a 28-day cycle.
9,359 studies on the registry are indexed under Neoplasms; 2,486 are open to participants now.
This study's enrollment of 47 is close to the median of 50 across 7,250 interventional studies indexed under Neoplasms.
Browse Neoplasms studies →Biogen is the lead sponsor of 494 studies on the registry; 22 are open to participants now.
Of its 98 completed or terminated interventional studies of FDA-regulated products, 49 (50%) have results posted.
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Exclusion Criteria:
Bardoxolone methyl to be taken orally for 21 consecutive days, once a day, in the morning prior to food intake. Patients to continue to receive treatment for the first 21 days of each 28-day cycle until they experience intolerable toxicity, show evidence of disease progression, or receive a maximum of 18 cycles (18 months).
Drug: Bardoxolone methyl
Also known as: RTA 402
To determine the dose-limiting toxicity, maximum tolerated dose, and recommended phase II dose of Bardoxolone methyl Capsules
Time frame: 28 day cycles, with a maximum of 18 cycles (18 months)
To characterize the pharmacokinetics of Bardoxolone methyl in this patient population.
Time frame: 28 day cycles, with a maximum of 18 cycles (18 months)
To document any preliminary antitumor activity.
Time frame: 28 day cycles, with a maximum of 18 cycles (18 months)
To determine the in vivo molecular and biological effects.
Time frame: 28 day cycles, with a maximum of 18 cycles (18 months)
To correlate the biological activity of RTA 402 with drug concentration in plasma and blood cellular elements.
Time frame: 28 day cycles, with a maximum of 18 cycles (18 months)
Plan to share: Yes — In accordance with Biogen's Clinical Trial Transparency and Data Sharing Policy on https://www.biogentrialtransparency.com/
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This study is completed, as verified in May 2025. You cannot join it, but the record below documents what was studied.
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