RecruitingPhase 1NCT07214662
A Study to Evaluate the Safety, Pharmacokinetics, and Activity of GDC-0587 as a Monotherapy and in Combination With Giredestrant in Participants With Locally Advanced or Metastatic Estrogen Receptor-Positive and Human Epidermal Growth Factor Receptor 2-Negative (ER+/HER2-) Breast Cancer
Studying Epidermal disease
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Genentech, Inc.
- Principal Investigator
- Clinical TrialsGenentech, Inc.
- Intervention
- GDC-0587(drug)
- Enrollment
- 136 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2026 – 2030
Study locations (4)
- START - Midwest - EDOS, Grand Rapids, Michigan, United States
- START - San Antonio - EDOS, San Antonio, Texas, United States
- National Taiwan University Hospital, Taipei, Taipei City, Taiwan
- National Cheng Kung University Hospital, Tainan, Taiwan
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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