Skip to main content
OpenTrials
Enrolling by Invitation

NCT Number: NCT01881503

Expanded Access Study of HBOC-201 (Hemopure) for the Treatment of Life-Threatening Anemia

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.

Enrolling by Invitation

Interested in participating?

Request Info

Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Englewood Hospital and Medical Center

Englewood, New Jersey, 07631, United States

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients > = 18 years of age
  • 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
  • Patients or their Legally Authorized Representatives who are able and willing to provide informed consent

Exclusion criteria

  • Patients with known hypersensitivity or allergy to beef products
  • 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)
  • Patients > 80 years of age (on a case by case and quality of life determination)
  • Patients who are eligible for blood transfusions

Treatment and study plan

HBOC-201

Biological

HBOC-201 is purified, cross-linked, acellular bovine hemoglobin (Hb) in a modified lactated Ringer's solution.

Other names: Hemopure

Primary outcomes

  1. survival

    Time frame: 1 week

    subjects will receive HBOC-201 to treat life-threatening anemia

Sponsors and collaborators

Lead sponsor

Englewood Hospital and Medical Center

Other

Collaborators

  • HbO2 Therapeutics LLC

Registry information

Official study title

Expanded Access Protocol for the Treatment Use of HBOC-201

Important dates

Study start
2013
Primary completion
2026
Study completion
2026
First posted
Jun 19, 2013
Registry last updated
Apr 13, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.