Long-term Follow-up of HLH Patients Who Received Treatment With NI-0501, an Anti-interferon Gamma Monoclonal Antibody
| Status: | Recruiting | 
|---|---|
| Conditions: | Hematology | 
| Therapuetic Areas: | Hematology | 
| Healthy: | No | 
| Age Range: | Any | 
| Updated: | 2/28/2019 | 
| Start Date: | June 2013 | 
| Contact: | Cristina de Min, MD | 
| Email: | cdemin@novimmune.com | 
| Phone: | +41 61 201 1322 | 
A Multicenter Study for the Long-term Follow-up of HLH Patients Who Received Treatment With NI-0501, an Anti-interferon Gamma Monoclonal Antibody
International, multicenter, long-term, follow-up study that will enroll HLH patients who have
received NI-0501 in a previous clinical trial, in the context of the clinical development
program for NI-0501
			received NI-0501 in a previous clinical trial, in the context of the clinical development
program for NI-0501
The aim of this study is to monitor the long-term safety profile of patients who have
previously received at least one dose of NI-0501, including survival at several time points
after the administration of NI-0501.
Moreover to study the elimination profile of NI-0501 and to assess the immunogenicity of
NI-0501.
Furthermore in the event that patients, upon request of the treating physician, will be
maintained on NI-0501 treatment beyond the foreseen 8 weeks, NI-0501 safety, tolerability,
efficacy and PK profile will be closely monitored in these patients until treatment
discontinuation.
previously received at least one dose of NI-0501, including survival at several time points
after the administration of NI-0501.
Moreover to study the elimination profile of NI-0501 and to assess the immunogenicity of
NI-0501.
Furthermore in the event that patients, upon request of the treating physician, will be
maintained on NI-0501 treatment beyond the foreseen 8 weeks, NI-0501 safety, tolerability,
efficacy and PK profile will be closely monitored in these patients until treatment
discontinuation.
Inclusion Criteria:
- Having received at least one dose of NI-0501.
- Having signed the Informed Consent by the patient or the patient's legal
representative(s), as applicable, with the assent of patients who are legally capable
of providing it.
Exclusion Criteria:
We found this trial at
    9
    sites
	
								Cincinnati, Ohio 45229			
	
			
					Principal Investigator: Michael Jordan, MD
			
						
										Phone: 513-636-7287
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								Chapel Hill, North Carolina 27599			
	
			(919) 962-2211 
							
					Principal Investigator: Kimberly Kasow, MD
			
						
										Phone: 919-962-8733
					
		University of North Carolina at Chapel Hill Carolina’s vibrant people and programs attest to the...  
  
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									1405 Clifton Road NE
Atlanta, Georgia 30322
	
			Atlanta, Georgia 30322
404-785-6000
							
					Principal Investigator: Shanmuganathan Chandrakasan, MD
			
						
										Phone: 404-727-8877
					
		Children's Healthcare of Atlanta Whether treating a toddler in an emergency or supporting a teen...  
  
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									13123 E 16th Ave
Aurora, Colorado 80045
	
			Aurora, Colorado 80045
(720) 777-1234
							
					Principal Investigator: Timothy Garrington, MD
			
						
										Phone: 720-777-6740
					
		Children's Hospital Colorado At Children's Hospital Colorado, we see more, treat more and heal more...  
  
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								Boston, Massachusetts 02115			
	
			
					Principal Investigator: Barbara A Degar, MD
			
						
										Phone: 617-632-5186
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								Houston, Texas 77030			
	
			
					Principal Investigator: Carl Allen, MD, PhD
			
						
										Phone: 832-824-4312
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								Münster,  48149			
	
			
					Principal Investigator: Claudia Rössig, Prof. Dr. Med.
			
						
										Phone: 0049 2518347742
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								Salt Lake City, Utah 84143			
	
			
					Principal Investigator: Mark N Fluchel, MD
			
						
										Phone: 801-662-4710
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								Wilmington, Delaware 19803			
	
			
					Principal Investigator: Jonathan Powell, MD
			
						
										Phone: 302-651-5500
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