Open
  
      Actively Recruiting
  
  A Phase 1 Study of AB521 Monotherapy and Combination Therapies in Renal Cell Carcinoma and Other Solid Tumors
About
Brief Summary
              
The purpose of this study is to evaluate the safety and tolerability of:
- casdatifan when taken alone in participants with advanced solid tumor malignancies and clear cell renal cell carcinoma (ccRCC) during the dose escalation stage; and
 - casdatifan monotherapy and casdatifan in combination with cabozantinib or zimberelimab in participants with ccRCC in the dose expansion stage
 
      Primary Purpose
    
          
      Study Type
    
          
      Phase
    
      Eligibility
      Gender
    
      
      Healthy Volunteers
    
      
      Minimum Age
    
      
      Maximum Age
    
      Key Inclusion Criteria:
- Must have at least one measurable lesion per RECIST guidance
 - Eastern Cooperative Oncology Group (ECOG) performance status score of ≤ 1
 - Disease-specific criteria for dose escalation:
- Participants may have any pathologically confirmed solid tumor type where no other treatment options are available
 - Creatinine clearance ≥ 40 mL/min Disease-specific criteria for dose-expansion:
 
 - Histologically confirmed ccRCC
 - Creatinine clearance ≥ 40 mL/min
 
Key Exclusion Criteria:
- Use of any live vaccines against infectious diseases (eg, influenza, varicella) within 4 weeks (28 days) of initiation of investigational product
 - Has any other clinically significant cardiac, respiratory, or other medical or psychiatric condition that might interfere with a participant's participation in the clinical study or make the administration of investigational product hazardous
 - History of trauma or major surgery within 28 days prior to the first dose of investigational product
 - For all expansion cohorts: prior treatment with an hypoxia inducible factor (HIF)-2α inhibitor. For the casdatifan + cabozantinib combination cohort, any prior treatment with cabozantinib
 - Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
 
Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Join this Trial
      Contact our clinical trial navigators for opportunities that may be suitable for you
    
  
      Study Stats
    
          
      Protocol No.
    
      23-001765
      
  
      Category
    
      Adolescent & Young Adults (AYA)
          Kidney Cancer
      
          Principal Investigator
        
        
          
      Contact
    
      
        Location
      
      - UCLA Santa Monica
 - UCLA Westwood