Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

3 clinical studies listed.

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Advanced CCNE1-amplified Solid Tumors

Tundra lists 3 Advanced CCNE1-amplified Solid Tumors clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT07288359

Study of GVV858 as a Single Agent or in Combination With Endocrine Therapy in Patients With HR+/HER2- Breast Cancer and Other Advanced Solid Tumors

Phase I: Characterize safety and tolerability of GVV858 as a single agent and in combination with fulvestrant or letrozole. Identify dose range for optimization/recommended dose for further clinical evaluation. Phase II: Further characterize the safety and tolerability of GVV858 in combination with fulvestrant in patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced breast cancer.

Gender: All

Ages: 18 Years - Any

Updated: 2026-05-27

2 states

Advanced HR+/HER2- Breast Cancer
Advanced CCNE1-amplified Solid Tumors
Metastatic Castration-resistant Prostate Cancer
NOT YET RECRUITING

NCT07570966

Study of ERW316 as a Single Agent or in Combination With Endocrine Therapy in Patients With HR+/HER2- Breast Cancer and Other Advanced Solid Tumors

Phase I: Characterize safety and tolerability of ERW316 as a single agent and in combination with fulvestrant or letrozole. Identify dose range for optimization/recommended dose for further clinical evaluation. Phase II: Further characterize the safety and tolerability of ERW316 in combination with fulvestrant in patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced breast cancer.

Gender: All

Ages: 18 Years - Any

Updated: 2026-05-06

Advanced HR+/HER2- Breast Cancer
Advanced CCNE1-amplified Solid Tumors
Metastatic Castration-resistant Prostate Cancer (mCRPC)
RECRUITING

NCT06726148

Study of ECI830 Single Agent or in Combination in Patients With Advanced HR+/HER2- Breast Cancer and Other Advanced Solid Tumors

Phase I: Characterize safety and tolerability of ECI830 as a single agent and in combination with ribociclib and fulvestrant. Identify dose range for optimization/recommended dose for future studies. Phase II: Assess the anti-tumor activity of ECI830 in combination with ribociclib and fulvestrant in patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced breast cancer.

Gender: All

Ages: 18 Years - 100 Years

Updated: 2026-04-27

17 states

Advanced HR+/HER2- Breast Cancer
Advanced CCNE1-amplified Solid Tumors