Condition: Glioma · Sponsor: Hangzhou Hanx Biopharmaceuticals, Ltd.
The study will include a dose-escalation and dose-expansion component to establish the recommended Phase 2 dose (RP2D) for HX301 in combination with Temozolomide and to evaluate the preliminary antitumor activity of HX301.HX301 is an investigational drug that has not yet been approved by the Food and Drug Administration (FDA) or any other regulatory authorities for commercial purposes.
This description comes directly from the study's public registry record.
Shuang Liu · +8618601689862 · shuang.liu@hanxbio.com
Always discuss trial participation with your own doctor first.
| Beijing Tiantan Hospital Capital Medical University | Beijing, Beijing Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06703255