This study is testing the safety and tolerability of BGB-21447 monotherapy in participants with relapsed or refractory (R/R) non-Hodgkin lymphoma (NHL) and chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). The study aims to determine the maximum tolerated dose (MTD), maximum administered dose (MAD), recommended Phase 2 dose (RP2D), and pharmacokinetic profile of the drug. Additionally, preliminary antitumor activity will be characterized. The study is divided into 2 main parts: Part 1 “Monotherapy Dose Finding” and Part 2 “Monotherapy Dose Optimization.”
Accelerate enrollment with targeted advertising campaigns
Step 1: Add a recruitment campaign (optional)
Our expert team has 10+ years running successful recruitment campaigns for clinical research sites
Your plan includes posting your clinical trials on our recruitment portal and mobile apps. Boost your trials with targeted advertising campaigns to reach more participants, faster.
What you get with a targeted campaign
We handle everything: audience targeting, creative development, geo targeting to your site locations, and ongoing optimizations. Qualified participant inquiries flow directly into your dashboard. Inquiries typically begin within a few days and continue throughout the campaign.
Select your study's therapeutic area and indication below. This helps us calculate accurate campaign budget and delivery timelines based on recruitment complexity.
Maximum participant inquiries available for this indication.
Cost per Inquiry
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Total Campaign Investment
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Estimated Campaign Duration
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Timeline varies based on campaign performance and audience targeting.