Protocol No. | UW24107 CPI-818-004 |
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Principal Investigator | Rajguru, Saurabh | ||
Phase | III | ||
Age Group | Adult | ||
ClinicalTrials.Gov | NCT06561048 (Click to jump to clinicaltrials.gov) | ||
Management Group(s) | Lymphoma | ||
Title
Description
Objective
Treatment This is a Phase 3, randomized, 2-arm, open-label, multicenter, stratified study of soquelitinib, an oral interleukin-2-inducible T cell kinase (ITK) inhibitor, versus physician's choice standard of care (SOC) treatment of either belinostat or pralatrexate in participants with relapsed/refractory (R/R) peripheral T-cell lymphoma not otherwise specified (PTCL-NOS), follicular helper T-cell lymphomas (FHTCLs), or systemic anaplastic large-cell lymphoma (sALCL). Approximately 150 participants will be randomized at a 1:1 ratio to the 2 treatment arms (soquelitinib or SOC) and will be stratified by region of the world, age, and time to relapse for the most recent prior therapy. Participants will receive study treatment for up to a maximum of 2 years, unacceptable toxicity, or disease progression, whichever is earlier. Participants randomized to receive SOC who have confirmation of progressive disease may have the opportunity to crossover to receive treatment with soquelitinib.
Key Eligibility
For full study eligibility, see this study's ClinicalTrials.gov record.
Applicable Disease Sites
Participating Institutions
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