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
Condition(s) studied
Investigational drug(s) / intervention(s)
GVV858: Experimental
Fulvestrant: Approved medication
Letrozole: Approved medication
Study summary
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.
Eligibility
Primary outcome measure(s)
- Phase I: Incidence and severity of dose-limiting toxicities (DLTs) — 28 days
Number of participants with DLTs. A DLT is defined as an adverse event or abnormal laboratory value of Common Terminology Criteria for Adverse Events (CTCAE) grade 3 or higher, unless clearly and inconvertibly assessed as due to disease progression, inter-current illness/injury, concomitant medications, or extraneous causes, that occurs within the first 28 days of treatment in the Phase 1 part. Other clinically significant toxicities may be considered to be DLTs, even if not CTCAE grade 3 or higher. - Phase I and phase II: Incidence and severity of adverse events (AEs) and serious adverse events (SAEs) — Up to approximately 2 years
Number of participants with AEs and SAEs, including changes in vital signs, electrocardiograms (ECGs) and laboratory values qualifying and reported as AEs. - Phase I and phase II: Frequency of dose interruptions, reductions and discontinuations — Up to approximately 2 years
Number of participants with dose adjustments (reductions, interruption, or permanent discontinuation) as a measure of tolerability. - Phase I and phase II: Dose intensity — Up to approximately 2 years
The dose intensity of each study drug is computed as the ratio of actual cumulative dose received and actual duration of exposure.
Trial sites (16)
| Facility | City | Region | Status |
|---|---|---|---|
| Emory University | Atlanta | Georgia | Recruiting |
| Tennessee Oncology PLLC | Nashville | Tennessee | Recruiting |
| START | San Antonio | Texas | Recruiting |
| Novartis Investigative Site | Toronto | Ontario | Recruiting |
| Novartis Investigative Site | Olomouc | Czechia | Recruiting |
| Novartis Investigative Site | Odense C | Denmark | Recruiting |
| Novartis Investigative Site | Pierre-Bénite | France | Recruiting |
| Novartis Investigative Site | Jena | Thuringia | Recruiting |
| Novartis Investigative Site | Essen | Germany | Recruiting |
| Novartis Investigative Site | Milan | MI | Recruiting |
| Novartis Investigative Site | Milan | MI | Recruiting |
| Novartis Investigative Site | Kyoto | Japan | Recruiting |
| Novartis Investigative Site | Singapore | Singapore | Recruiting |
| Novartis Investigative Site | Barcelona | Spain | Recruiting |
| Novartis Investigative Site | Madrid | Spain | Recruiting |
| Novartis Investigative Site | Taipei | Taiwan | Recruiting |
More Novartis Pharmaceuticals trials in Japan
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07288359 on ClinicalTrials.gov ↗ ← All trials in Japan