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Recruiting Phase 1 NCT06220864

SNV1521 in Participants With Advanced Solid Tumors

Phase 1 – testing safety in a small group of people
Conditions: Advanced Solid Tumor

Sponsor: Synnovation Therapeutics, Inc.

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Overview
This study is testing a new medicine, SNV1521, for people with advanced cancers. The researchers want to find out if SNV1521 is safe, well-tolerated, and effective in treating solid tumors. They are investigating different doses in order to find the most effective and safe one. They are also investigating whether it can be combined with other cancer therapies.
Who can participate
Inclusion Criteria: * Advanced or metastatic solid tumor malignancy * Evaluable or Measurable disease (RECIST 1.1 Criteria). * ECOG Performance Status 0 or 1. * Life expectancy \> 3 months Exclusion Criteria: * History of other malignancy within the past 2 years * Prior diagnosis of Myelodysplastic syndrome or Acute Myeloid Leukemia * Significant cardiovascular disease within 6 months * Significant gastrointestinal disease * HIV infection with a CD4+ T-cell count \< 200 cells/μL and/or a detectable viral load * Liver dysfunction
Locations 6
Australia (1)
Scientia Clinical Research
Randwick , New South Wales
Canada (1)
Arthur J.E. Child Comprehensive Cancer Centre
Calgary , Alberta
France (1)
Institut Bergonie
Bordeaux
Italy (1)
Istituto Clinico Humanitas
Milan
Spain (1)
NEXT Oncology - Barcelona
Barcelona
United States (1)
Smilow Cancer Hospital at Yale New Haven
New Haven , Connecticut
Technical details
Status
Recruiting
Phase
Phase 1
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
23.02.2024
Completion date
01.12.2027
Registry ID
NCT06220864
Source
anzctr
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Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.