Condition: Advanced Solid Tumors With MAPK Pathway Mutations · Sponsor: D3 Bio (Wuxi) Co., Ltd
This first-in-human (FIH) study aims to assess the safety, tolerability, pharmacokinetics, and recommended phase 2 dose (RP2D) of D3S-002 given orally daily for 21-day cycles in adult subjects with advanced solid tumors with mitogen-activated protein kinase (MAPK) pathway mutations.
This description comes directly from the study's public registry record.
Medical Director · +86 21 61635900 · D3bio_CT@d3bio.com
Always discuss trial participation with your own doctor first.
| D3 Bio Investigative Site | Detroit, Michigan, United States | Recruiting |
| D3 Bio Investigative Site | New York, New York, United States | Completed |
| D3 Bio Investigative Site | Nashville, Tennessee, United States | Recruiting |
| D3 Bio Investigative Site | Blacktown, New South Wales, Australia | Completed |
| D3 Bio Investigative Site | Macquarie Park, New South Wales, Australia | Recruiting |
| D3 Bio Investigative Site | Bedford Park, South Australia, Australia | Completed |
| D3 Bio Investigative Site | Nedlands, Western Australia, Australia | Completed |
| D3 Bio Investigative Site | Beijing, Beijing Municipality, China | Recruiting |
| D3 Bio Investigative Site | Guangzhou, Guangdong, China | Recruiting |
| D3 Bio Investigative Site | Harbin, Heilong Jiang, China | Completed |
| D3 Bio Investigative Site | Wuhan, Hubei, China | Recruiting |
| D3 Bio Investigative Site | Shanghai, Shanghai Municipality, China | Active Not Recruiting |
+ 2 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT05886920