A Study of ERAS-4001 in Patients With Advanced or Metastatic Solid Tumors.
Part of paid clinical trials in Nashville, Tennessee.
- Sponsor
- Erasca, Inc.
- Study ID
- NCT07021898
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Metastatic Solid Tumors
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 99 Years
- Healthy Volunteers
- Not accepted
Interventions
- ERAS-4001 — DRUGERAS-4001 Administered orally
- ERAS-4001 in combination — DRUGERAS-4001 Administered orally and in combination with either Keytruda (pembrolizumab) via IV administration or Vectibix (panitumumab) via IV administration.
Study Details
The main purpose of the study is to assess whether the study drug, ERAS-4001, is safe and tolerable when administered to patients with advanced or metastatic solid tumors with certain KRAS mutations. ERAS-4001 will be given alone or in combination with other treatments.
Key Dates
- Start date
- Aug 6, 2025
- Status verified
- Dec 2025
- Primary completion
- Aug 31, 2028
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 200 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: ERAS-4001 Monotherapy Dose Optimization.Escalating doses of ERAS-4001 administered orally.
- Experimental: ERAS-4001 Combination Dose OptimizationERAS-4001 administered orally with another investigational agent.
Primary Outcome Measure
Dose Limiting Toxicities (DLT) [ Time Frame: Study Day 1 up to Day 21 ]
Central Contacts
- Erasca Clinical Team+1-858-465-6511
- Les Brail, Study Director, PhD
Locations (5)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Sarah Cannon Research Institute (SCRI) Oncology Partners | Nashville | Tennessee | 32703 | - |
| The University of Texas MD Anderson Cancer Center | Houston | Texas | 77030 | - |
| NEXT Oncology | Irving | Texas | 75039 | - |
| NEXT Oncology | San Antonio | Texas | 78229 | - |
| Fred Hutchinson Cancer Center | Seattle | Washington | 98109 | - |
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