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A Study of ERAS-0015 in Patients With Advanced or Metastatic Solid Tumors

← catalyst calendar

NCT06983743 · readout in 620 d

Sponsored by Erasca, Inc. (industry) · ERAS — their whole pipeline →. With Merck Sharp & Dohme LLC.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
600estimated
Sites
8
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-06-05actualWhen the study began enrolling
Primary completion2028-05-01estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-12-01estimatedThe whole study's end, after follow-up
First posted2025-05-21actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-31actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Metastatic Solid Tumors

Interventions

  • Drug: ERAS-0015
  • Drug: ERAS-0015 in combination — also filed as pembrolizumab, KEYTRUDA ®, panitumumab, Vectibix, gemcitabine, Gemzar, nab-paclitaxel, Abraxane

Primary outcomes

what the primary-completion date above is the date OF
Dose Limiting Toxicities (DLT)
measured Study Day 1 up to Day 21
Maximum tolerated dose (MTD)
measured Study Day 1 up to Day 21
Recommended dose for expansion (RDE)
measured Study Day 1 up to Day 21
Adverse Events
measured Study Day 1 up to Day 21
Plasma concentration (Cmax)
measured Study Day 1 up to 65
Time to achieve Cmax (Tmax)
measured Study Day 1 up to 65
Area under the curve
measured Study Day 1 up to 65
Half-life
measured Study Day 1 up to 65

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