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Study identifier: NCT05886920 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Phase 1/2 Study of D3S-002 as Monotherapy or Combination Therapy in Adult Subjects With Advanced Solid Tumors With MAPK Pathway Mutations

Condition: Advanced Solid Tumors With MAPK Pathway Mutations  ·  Sponsor: D3 Bio (Wuxi) Co., Ltd

PhasePhase 1/Phase 2
Planned participants67
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

Talk to the study team

Medical Director  ·  +86 21 61635900  ·  D3bio_CT@d3bio.com

Always discuss trial participation with your own doctor first.

Locations (14)

D3 Bio Investigative SiteDetroit, Michigan, United StatesRecruiting
D3 Bio Investigative SiteNew York, New York, United StatesCompleted
D3 Bio Investigative SiteNashville, Tennessee, United StatesRecruiting
D3 Bio Investigative SiteBlacktown, New South Wales, AustraliaCompleted
D3 Bio Investigative SiteMacquarie Park, New South Wales, AustraliaRecruiting
D3 Bio Investigative SiteBedford Park, South Australia, AustraliaCompleted
D3 Bio Investigative SiteNedlands, Western Australia, AustraliaCompleted
D3 Bio Investigative SiteBeijing, Beijing Municipality, ChinaRecruiting
D3 Bio Investigative SiteGuangzhou, Guangdong, ChinaRecruiting
D3 Bio Investigative SiteHarbin, Heilong Jiang, ChinaCompleted
D3 Bio Investigative SiteWuhan, Hubei, ChinaRecruiting
D3 Bio Investigative SiteShanghai, Shanghai Municipality, ChinaActive Not Recruiting

+ 2 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05886920