Study Name: A Phase 2b/3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Combined Dose-Finding and Cardiovascular Outcome Study to Investigate the Efficacy and Safety of CSL300 (Clazakizumab) in Subjects with End Stage Kidney Disease Undergoing Dialysis.
Sponsor Name: CSL Behring LLC
Study Phase: Phase III
Status: Enrollment on-going.
Investigational Product: CSL-300 (monoclonal antibody against IL-6)
Primary Objective: To evaluate the efficacy of CSL300 on reducing the risk of CV events (composite endpoint of CV death and MI).
Primary Endpoint: Time to first occurrence of CV death or MI.
Principal Investigator: Dr. Jodumutt G. Bhat
Study Name: A Phase I/III Randomized, Double-Blind, Active Controlled Study to Evaluate the Efficacy and Safety of AZD3152 for Pre-Exposure Prophylaxis of COVID-19 in Participants with Conditions Causing Immune Impairment
Sponsor Name: AstraZeneca
Study Phase: Phase III
Status: Ongoing. Enrollment is closed.
Investigational Product: AZD3152 (a monoclonal Ab) 300 mg single IM dose (300 mg Placebo + 300 mg AZD3152)
AZD7442 (EVUSHELD) (a monoclonal Ab) 600 mg single IM dose (300 mg AZD1061 + 300 mg AZD8895)
Primary Objective: To evaluate the safety and efficacy of AZD3152 in adults and adolescents 12 years of age and older with immune impairment.
Principal Investigator: Dr. Jodumutt G. Bhat
Study Name: A Randomized Parallel-group, Placebo-controlled, Double-blind, Event-driven, Multi-center Phase 2 Clinical Outcome Trial of Prevention of Arteriovenous Graft Thrombosis and Safety of MK-2060 in Patients with End Stage Renal Disease Receiving Hemodialysis.
Sponsor Name: Merck, Sharp and Dohme Corp.
Study Phase: Phase II
Status: Ongoing. Enrollment is closed.
Investigational Product: MK-2060 (monoclonal antibody against Factor XI)
Primary Objective: The purpose of this study is to evaluate the efficacy and safety of two different doses of MK-2060 (a monoclonal antibody against Factor XI) in end stage renal disease (ESRD) participants receiving hemodialysis via an arteriovenous graft (AVG).
Primary Endpoint: Time to First AVG Thrombosis Event: From date of randomization until the date of first occurrence of an AVG thrombosis event, assessed up to approximately 17 months.
Principal Investigator: Dr. Jodumutt G. Bhat
Study Name: Effects of Ziltivekimab Versus Placebo on Cardiovascular Outcomes in Participants With Established Atherosclerotic Cardiovascular Disease, Chronic Kidney Disease and Systemic Inflammation.
Sponsor: Novo Nordisk
Study Phase: Phase III
Status: Ongoing. Enrollment is closed.
Investigational Product: Ziltivekimab (human monoclonal Ab to IL-6) 15 mg/mL (1 mL) s.c. once monthly
Primary Objective: To demonstrate the superiority of Ziltivekimab in reducing the risk of MACE compared to placebo in patients with ASCVD, CKD and systemic inflammation.
Primary Endpoint: Time from randomization to first occurrence of MACE.
Principal Investigator: Dr. Jodumutt G. Bhat