Trials / Recruiting
RecruitingNCT06980532
Glumetinib Combined With Fruquintinib in the Treatment of MET Amplification or Protein Overexpression in Third-Line Unresectable Metastatic Colorectal Cancer
Glumetinib Combined With Fruquintinib in the Treatment of MET Amplification or Protein Overexpression in Third-Line Unresectable Metastatic Colorectal Cancer: A Prospective, Exploratory, Open-Label Clinical Study
- Status
- Recruiting
- Phase
- Phase 1 / Phase 2
- Study type
- Interventional
- Enrollment
- 42 (estimated)
- Sponsor
- Liu Huang · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Glumetinib combined withFruquintinib in the treatment of MET amplification or protein overexpression in third-line unresectable metastatic colorectal cancer: evaluation of efficacy and safety
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Glumetinib Combined with Fruquintinib | Fruquintinib: 3mg, po.qd, d1-14,q3w; Guemitinib: Grade 1:200mg, po, qd, q3w; Grade 2:250mg, po, qd, q3w; Phase I: The dose of Glumetinib (200 mg → 250 mg) is dynamically adjusted using the "3+3 dose-escalation rule" to determine the optimal dose of Fruquintinib. Phase II: The RP2D (Recommended Phase II Dose) of Glumetinib identified in Phase I is continued in combination with Fruquintinib. |
Timeline
- Start date
- 2025-04-25
- Primary completion
- 2028-12-30
- Completion
- 2028-12-30
- First posted
- 2025-05-20
- Last updated
- 2025-05-20
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06980532. Inclusion in this directory is not an endorsement.