Clin2
NCT03720626Worth exploringAvailable

Access program for crizanlizumab for sickle cell disease

Sickle Cell Disease

Treatments studied

Part of Blood & lymphatic, Genetic & congenital clinical trials.

This program provides crizanlizumab, a medicine that may help reduce pain crises in sickle cell disease, to patients who have no other treatment options and cannot join a clinical trial. It is a special access program for individual patients.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Ages
12 years to 70 years
Study type
Expanded Access

Who can take part

  • You have a serious or life-threatening condition, such as sickle cell disease.
  • There is no other satisfactory treatment available for your condition.
  • You are not eligible for or cannot participate in a clinical trial.
  • Your doctor has requested this medicine for you and believes it may help.
  • The medicine is allowed in your country and will not interfere with ongoing studies.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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