Erasca, Inc. (ERAS)
Erasca, Inc. is a biopharmaceutical company in the clinical development stage, primarily focused on identifying, advancing, and commercializing therapeutic solutions for malignancies propelled by the RAS/MAPK pathway. The firm's pipeline features several key experimental drugs: ERAS-007, an orally administered ERK1/2 inhibitor designed to address non-small cell lung cancer, colorectal cancer, and acute myeloid leukemia; and ERAS-601, an oral SHP2 inhibitor targeting patients with advanced or metastatic solid tumors. Additionally, Erasca is progressing ERAS-801, an EGFR inhibitor capable of penetrating the central nervous system, intended for recurrent glioblastoma multiforme. The company was founded in 2018 and maintains its headquarters in San Diego, California.
Sector: Pharmaceutical Preparations
Industry: Biotechnology
Erasca, Inc.
Trials need funding. See this company's dilution risk and cash position.
- Phase 3Active, not recruiting
A Study to Assess Naporafenib (ERAS-254) Administered With Trametinib in Patients With NRAS-mutant Melanoma (SEACRAFT-2)
Naporafenib, Dacarbazine
Advanced or Metastatic NRAS-mutant Melanoma
NCT06346067Enrollment78StartApr 2024Primary CompletionApr 2028est.CompletionDec 2028est. - Phase 1/2Completed
A Study of ERAS-007 as Monotherapy or in Combination With ERAS-601 in Patients With Advanced or Metastatic Solid Tumors
ERAS-007, ERAS-601
Advanced or Metastatic Solid Tumors
NCT04866134Enrollment85StartMay 2021Primary CompletionJul 2026CompletionJul 2026 - Phase 1/2Completed
A Study of ERAS-007 in Patients With Advanced Gastrointestinal Malignancies
ERAS-007, Encorafenib
Metastatic Colorectal Cancer, Metastatic Pancreatic Ductal Adenocarcinoma
NCT05039177Enrollment101StartSep 2021Primary CompletionAug 2025CompletionJan 2026 - Phase 1/2Withdrawn
A Study of Anti-Cancer Therapies Targeting the MAPK Pathway in Patients With Hematologic Malignancies
ERAS-007, ERAS-601
Acute Myeloid Leukemia
NCT05279859Enrollment0StartMar 2022est.Primary CompletionMar 2025est.CompletionJun 2025est. - Phase 1Completed
A Dose Escalation/Expansion Study of ERAS-601 in Patients With Advanced or Metastatic Solid Tumors
ERAS-601, Cetuximab
Advanced or Metastatic Solid Tumors
NCT04670679Enrollment90StartDec 2020Primary CompletionFeb 2026CompletionJun 2026 - Phase 1Completed
A Study of Anti-Cancer Therapies Targeting the MAPK Pathway in Patients With Advanced NSCLC
ERAS-007, ERAS-601
Advanced Non-squamous Non-small-cell Lung Cancer
NCT04959981Enrollment24StartSep 2021Primary CompletionApr 2023CompletionApr 2023 - Phase 1Active, not recruiting
A Study to Assess Naporafenib (ERAS-254) Administered With Trametinib in Patients With RAS Q61X Mutations
Naporafenib, Trametinib
Advanced or Metastatic Solid Tumors
NCT05907304Enrollment86StartAug 2023Primary CompletionJul 2025CompletionDec 2026est. - Phase 1Recruiting
A Study of ERAS-0015 in Patients With Advanced or Metastatic Solid Tumors
ERAS-0015, ERAS-0015 in combination
Metastatic Solid Tumors
NCT06983743Enrollment600StartJun 2025Primary CompletionMay 2028est.CompletionDec 2028est. - Phase 1Recruiting
A Study of ERAS-4001 in Patients With Advanced or Metastatic Solid Tumors.
ERAS-4001, ERAS-4001 in combination
Metastatic Solid Tumors
NCT07021898Enrollment200StartAug 2025Primary CompletionAug 2028est.CompletionDec 2028est.
| Drug / Therapy | Link | ||
|---|---|---|---|
| Phase 3 | Active, not recruiting | Naporafenib, Dacarbazine | NCT06346067 |
| Phase 1/2 | Completed | ERAS-007, ERAS-601 | NCT04866134 |
| Phase 1/2 | Completed | ERAS-007, Encorafenib | NCT05039177 |
| Phase 1/2 | Withdrawn | ERAS-007, ERAS-601 | NCT05279859 |
| Phase 1 | Completed | ERAS-601, Cetuximab | NCT04670679 |
| Phase 1 | Completed | ERAS-007, ERAS-601 | NCT04959981 |
| Phase 1 | Active, not recruiting | Naporafenib, Trametinib | NCT05907304 |
| Phase 1 | Recruiting | ERAS-0015, ERAS-0015 in combination | NCT06983743 |
| Phase 1 | Recruiting | ERAS-4001, ERAS-4001 in combination | NCT07021898 |