Bleeding Clinical Trial
Official title:
Thrombosomes for Expanded Access Use
NCT number | NCT04619108 |
Other study ID # | Thrombosomes Expanded Access |
Secondary ID | |
Status | No longer available |
Phase | |
First received | |
Last updated |
Verified date | March 2024 |
Source | Cellphire Therapeutics, Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Expanded Access |
Expanded use of Thrombosomes where a clinical trial with Thrombosomes is not an option, Cellphire may elect to provide the Sponsor/Investigator (S/I) expanded access to its investigational product, Thrombosomes.
Status | No longer available |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. Subject has presented with WHO Grade 2 or higher bleeding which requires treatment with platelet therapy and there is limited availability of platelets or no other approved clinical alternative. 2. Evidence from the facility blood bank/Medical Director that there are no approved platelet products available for transfusion, or the patient is refractory to platelet transfusion. Exclusion Criteria: 3. Clinical circumstances of a history of thrombosis, thromboembolism, or vascular occlusion/ischemia in the prior six months such as defined by a past history of current diagnosis of one or more of the following: - arterial or venous thromboembolic disease including acute coronary syndrome - peripheral vascular disease - arterial or venous thrombosis (except when a prior history of central line thrombosis has resolved) - myocardial infarction (MI) - stent placement - valve replacement and/or repair - sinusoidal obstruction syndrome (veno-occlusive disease) |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Cellphire Therapeutics, Inc. |
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