Belleville, New Jersey Clinical Trials

A listing of Belleville, New Jersey clinical trials actively recruiting patient volunteers.

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Found 124 clinical trials
Q1212  

sas

New york
 (9.9 away)
  • 0 views
  • 19 Feb, 2024
  • +1 other locations
Trial_Creation Email  

sdf

sadad
 (9.9 away)
  • 0 views
  • 19 Feb, 2024
  • +5 other locations
Trial T2 V6.11-Formal Test  

qa

investigational site AUSTRALIA1
 (9.8 away)
  • 0 views
  • 19 Feb, 2024
  • +3 other locations
iConnect R12.3 UAT Dry Run Script 03-1  

iConnect R12.3 UAT Dry Run Script 05-1<br>

TrialX Research Center
 (9.9 away)
  • 0 views
  • 08 May, 2025
  • 1 location
iConnect R12.3.1 UAT Dry Run for Site Question  

iConnect R12.3.1 UAT Dry Run for Site Question

TrialX Research Center
 (9.9 away)
  • 0 views
  • 17 Apr, 2024
  • +1 other locations
6.14 Program Trial 1 - [18 to 35 yo]

6.14 Program Trial 1 - [18 to 35 yo]

TrialX Research Center
 (9.9 away) Contact site
  • 0 views
  • 04 Aug, 2024
  • 1 location
6.14 Program Trial 2 - [36 to 65 yo]

 6.14 Program Trial 1 - [36 to 65 yo]

TrialX Research Center
 (9.9 away) Contact site
  • 0 views
  • 23 Apr, 2024
  • 1 location
6.14 Program Trial 3 - [over 65 yo]

6.14 Program Trial 3 - [over 65 yo]

TrialX Research Center
 (9.9 away) Contact site
  • 0 views
  • 24 Apr, 2024
  • 1 location
Fitusiran Prophylaxis in Male Pediatric Subjects Aged 1 to Less Than 12 Years With Hemophilia A or B

Primary Objective: To confirm appropriate dose levels of fitusiran when administered to male pediatric participants (ages 1 to <12 years of age) with severe hemophilia A or B Secondary Objective: To characterize the safety and tolerability To characterize the pharmacokinetics (PK)

haemophilia a
factor ix
antihemophilic factor
bethesda assay
hemophilia
Investigational Site Number 8400008
 (8.8 away) Contact site
  • 0 views
  • 19 Feb, 2024
  • +10 other locations
Multi-center Open-label Phase 1b Study in Patients With Relapsed/Refractory Multiple Myeloma (RRMM)

Primary Objectives: To evaluate the safety and tolerability of isatuximab administered subcutaneously (SC) versus intravenously (IV) To evaluate the pharmacokinetics (PK) of SC and IV isatuximab Secondary Objectives: To estimate absolute bioavailability of SC and IV isatuximab To measure receptor occupancy (RO) after isatuximab SC versus IV administration To assess …

hepatitis
tuberculosis
hepatitis a
hydrochloride salt
arginine
Investigational Site Number 8400006
 (8.8 away) Contact site
  • 0 views
  • 24 Nov, 2025
  • +13 other locations