Sutacimig for Glanzmann Thrombasthenia
(SOLARA Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
Glanzmann thrombasthenia (GT) is a serious inherited bleeding disorder. In GT, platelets, the blood cells that normally stick together at the site of an injury to stop bleeding, are unable to properly do so. As a result, bleeding does not stop as it should. Bleeding in GT often starts without warning, can happen frequently, and can be severe. It most commonly affects the nose, mouth and gums, gastrointestinal tract, and skin, and many women and girls with GT experience heavy menstrual bleeding. Over time, bleeding can lead to iron deficiency and anemia. Some bleeding episodes require emergency care, hospitalization, transfusion, or surgery, and some can be life-threatening.
Sutacimig is an investigational medicine given as an injection under the skin (subcutaneous injection). It is designed to help platelets work at the site of bleeding despite the underlying defect in GT. It is intended to be given regularly to help prevent bleeding (prophylaxis), rather than only to treat bleeding after it starts.
The purpose of this study is to find out whether sutacimig, given as prophylaxis, reduces the number of treated bleeding episodes in people with GT compared with no prophylaxis, and to evaluate its safety and tolerability.
Who Is on the Research Team?
Medical Director
Principal Investigator
Hemab
Are You a Good Fit for This Trial?
This trial is for people diagnosed with Glanzmann thrombasthenia, a rare inherited bleeding disorder. Participants should be experiencing frequent or severe bleeding episodes and need regular treatment to prevent these bleeds.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- Sutacimig
Trial Overview
The study tests sutacimig, an experimental medicine given by injection under the skin, to see if it can help prevent bleeding in people with Glanzmann thrombasthenia compared to not receiving preventive treatment.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Participants will receive sutacimig 0.2 milligrams per kilogram (mg/kg) by subcutaneous injection once weekly for 48 weeks. Upon completion of the 48-week treatment period, participants will be offered the opportunity to transition to a separate open-label extension (OLE) study for continued assessment of the prophylactic treatment with sutacimig.
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Who Is Running the Clinical Trial?
Hemab ApS
Lead Sponsor
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