Expanded Access Study of HBOC-201 (Hemopure) for the Treatment of Life-Threatening Anemia
Status: | Enrolling by invitation |
---|---|
Conditions: | Anemia |
Therapuetic Areas: | Hematology |
Healthy: | No |
Age Range: | 18 - 80 |
Updated: | 8/8/2018 |
Start Date: | October 2013 |
End Date: | July 2020 |
Expanded Access Protocol for the Treatment Use of HBOC-201
The purpose of this expanded access study is to be able to provide treatment with HBOC-201 to
patients with life-threatening anemia for whom blood is not an option.
HBOC-201 is not FDA approved for use in the United States, but is approved as an oxygen
carrier in South Africa and Russia.
patients with life-threatening anemia for whom blood is not an option.
HBOC-201 is not FDA approved for use in the United States, but is approved as an oxygen
carrier in South Africa and Russia.
i. Initial Dose
For patients with a hemoglobin level less than 6 mg/dl, an initial dose of 32.5 g (one unit)
of HBOC 201 is recommended, to be followed by infusion of additional units as necessary to
achieve and maintain a total hemoglobin concentration above 6 g/dl, provided that the
patient's circulatory volume is properly controlled and will not impose an inappropriate
risk.
ii. Subsequent Doses
The need for additional dose administration should be assessed after each infusion as
clinically indicated.
Dosing will be stopped if any one of the following occurs:
- resolution of critical ischemia
- death
- recovery of native Hemoglobin levels to > 6 g/dL,
- evidence of reticulocytosis
For patients with a hemoglobin level less than 6 mg/dl, an initial dose of 32.5 g (one unit)
of HBOC 201 is recommended, to be followed by infusion of additional units as necessary to
achieve and maintain a total hemoglobin concentration above 6 g/dl, provided that the
patient's circulatory volume is properly controlled and will not impose an inappropriate
risk.
ii. Subsequent Doses
The need for additional dose administration should be assessed after each infusion as
clinically indicated.
Dosing will be stopped if any one of the following occurs:
- resolution of critical ischemia
- death
- recovery of native Hemoglobin levels to > 6 g/dL,
- evidence of reticulocytosis
Inclusion Criteria:
1. Patients > = 18 years of age
2. Patients with hemoglobin < = 8g/dL with with active bleeding, physiologic evidence of
critical ischemia, for example: elevated troponins, altered mental status, acute renal
failure, lactic acidosis or central nervous system supply dependency
3. Patients or their Legally Authorized Representatives who are able and willing to
provide informed consent
Exclusion Criteria:
1. Patients with known hypersensitivity or allergy to beef products
2. Patients with pre-existing uncontrolled hypertension, heart failure, renal failure,
circulatory hypervolemia or systemic mastocytosis (on a case by case and quality of
life determination)
3. Patients > 80 years of age (on a case by case and quality of life determination)
4. Patients who are eligible for blood transfusions
We found this trial at
1
site
350 Engle St
Englewood, New Jersey 07631
Englewood, New Jersey 07631
(201) 894-3000
Principal Investigator: Aryeh Shander, MD
Phone: 201-894-3418
Englewood Hospital and Medical Center Englewood Hospital was incorporated in 1888 as a non-profit, non-sectarian...
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