Pharmabiz
 

Pluristem develops PLX-RAD cells for use in haematology

Haifa, IsraelThursday, May 9, 2013, 17:00 Hrs  [IST]

Pluristem Therapeutics Inc., a leading developer of placenta-based cell therapies, has identified its first clinical indication in the haematology field for its Placental eXpanded (PLX) RAD cells for the enhancement of the engraftment of Hematopoietic Stem Cells (HSC) in patients experiencing a delay or failure of their bone marrow transplant (BMT). This follows Pluristem’s completion of additional pre-clinical studies showing promising results for PLX-RAD for this indication.

According to the National Marrow Donor Programme, an estimated 25,000 allogeneic bone marrow transplants are performed annually worldwide. Approximately 15 per cent of these patients will either have a delay or failure to engraft the HSCs, resulting in a condition that is life threatening, expensive and often requires the continued support of the patient with blood products. PLX-RAD may be beneficial to these patients.

PLX-RAD is currently being evaluated by the US National Institute of Allergy and Infectious Diseases (NIAID), a division of the US National Institutes of Health, in models of the acute radiation syndrome (ARS).

PLX-RAD, Pluristem’s second product candidate, joins PLX-PAD that is in clinical trials for the treatment of peripheral artery disease, muscle injury and Pulmonary Hypertension. Both product candidates are derived from placental raw material. The placenta is a very rich source for a variety of cells and Pluristem differentiates these products through the use of different cell populations combined with its proprietary 3D bioreactor manufacturing process that allows the company to change but precisely control the environment in which the cells grow. This results in a stable, consistent change to the therapeutic protein secretion profile of the cell that constitutes the difference between PLX-PAD and PLX-RAD. Pluristem intends to develop additional PLX products by capitalizing on these unique competitive advantages.

PLX-RAD cells have been shown to have an immunomodulatory effect via the secretion of cytokines and proteins that are known to stimulate Hematopoietic Stem Cells (HSC) to enhance the production of white blood cells, red blood cells and platelets. There was also evidence of a significant improvement in the recovery of these three blood lineages in bone marrow deficient animals compared to control animals.

Zami Aberman, chairman and CEO stated, “We are very excited to enter the field of haematology with our new PLX-RAD cell product candidate. PLX-RAD’s unique protein secretion profile enables its use in bone marrow deficiency syndromes. This unique characteristic will enable us to provide a product candidate that enables the recovery of the three blood lineages, potentially positioning PLX-RAD as first line treatment in a variety of bone marrow deficiencies.”

The essential element in BMT is the transplantation of Hematopoietic Stem Cells (HSC), the precursor of the formed elements of the blood (red cells, white cells and platelets). BMT is commonly used in the treatment of hematological malignancies to reconstitute the patient’s bone marrow after their diseased marrow is eradicated with chemo or radiotherapy. Approximately 15 per cent of patients undergoing BMT will either have a significant delay or failure to engraft the HSCs contained in the BMT, a condition that is life threatening, expensive and often requires the continued support of the patient with blood products. After demonstrating a significant enhancement of HSC engraftment in animals and in three patients with BMT failure where PLX cells were administered under a compassionate use programme, the company established a Haematology Clinical Advisory Board comprised of thought leaders in haematology throughout the world.

Pluristem Therapeutics Inc. is a leading developer of placenta-based cell therapies. The Company’s patented PLX (PLacental eXpanded) cells are a drug delivery platform that releases a cocktail of therapeutic proteins in response to a host of local and systemic inflammatory and ischemic diseases.

 
[Close]