Celavie Biosciences

Celavet Animal Health

Celavet Product Development

Celavet’s product development is geared towards enabling injured horses to regain their fullest potential as competitors, performers, workers, and companions. In 2012, the global equine healthcare market was recorded at US$26.6 billion (Transparency Market Research).

Offering a fast path to market, Celavet’s stem cell therapies are in development with applications for tendon and ligament injuries. Our products for the treatment and prevention of orthopedic injuries will have value in the veterinary marketplace.

Disease Candidate Preclinical Clinical
Tendinitis (e.g., tendon injuries, bowed tendons, ect.) Equine    
Musculoskeletal injuries Equine    
Osteoarthritus Canine  
Ligaments tendons Canine  
Burns Canine  
Kidney Desease Feline  

Products in Celavet Pipeline

Celavet has 3 sets of cultured stem cell lines:

  • Equine cells (OK100) for the treatment of musculoskeletal injuries
  • Canine cells (OK200) for the treatment of musculoskeletal injuries, wounds and burns
  • Feline cells (OK300)

The Center for Veterinary Medicine (CVM) approved Celavet’s equine donor screening protocol and cell product characterization (2017).

Our equine OK100 stem cells were successfully tested in a double-blind, controlled study at Cornell University’s Large Animal Lab by Principal Investigator Dr. Alan Nixon, DVM, BVSc, MS.

Ultrasonographical and morphological results showed:

  • Complete reconstruction of the experimental lesion
  • Anatomically correct fiber alignment as shown by ultrasound
  • Progressive healing in ESC injected tendons
  • Persisting echolucent core lesion in the control group
  • Increasing deterioration of lesion in the control group
  • All horses injected with ESCs demonstrating ultrasonographic evidence of improvement in healing

The figure above shows examples of the ultrasonographic healing progression between Horse 6 (ESC, treated with equine undifferentiated stem cells OK100) and Horse 5 (Control-sham injection). (Watts A, Yeager A, Kopyov O, Nixon A. Fetal derived embryonic-like stem cells improve healing in a large animal flexor tendonitis model. Stem Cell Research & Therapy. 2011 Jan 27;2(1):4.)

As a part of evaluating safety of OK99 stem cells for human use, Celavie Biosciences contracted Seventh Wave Laboratories, LLC (Chesterfield, MO) to perform a study, “Does Intraparenchymal Injection of Canine Allogeneic Stem Cells into the Canine Brain Elicit Immune Response.” To study the immunogenicity of Celavie stem cells in the same species environment, our canine stem cells were transplanted into the brains of healthy beagles. The blood and brain tissue were examined for signs of immune reaction to the cells. No immune response to OK99 stem cells was detected.

To further explore canine treatments, the following pilot study under IND OK200 was conducted: “An Open Label Study to Test the Safety and Efficacy of Fetal-derived Allogeneic Canine Stem Cells for the Treatment of Chronic Osteoarthritis and Cruciate Ligament Injuries in Canines.”

IND 012-003 was issued in January 2011, in which:

  • Eight dogs with chronic osteoarthritis were injected intravenously
  • In 12 dogs, the cells were injected directly into the joints
  • No tumor formation or infection was detected

The study was put on hold to concentrate efforts on the human and equine project.

Case Study: Wounds and Burns

Pre Surgery – July 26, 2011

Pre Surgery – July 26, 2011

Post Surgical – September 13, 2011

Post Surgical – September 13, 2011

Bernie was an abused pit bull whose owner left him on the metal roof of a row home in Reading, PA for several scorching hot summer days during which temperatures reached 110°F. He developed severe third-degree burns to all four paws (no skin remaining), as well as burns to his back and legs. The local director of the Animal Rescue League came to Celavet because of our pilots with stem cells and asked us to help this animal.

After CVM approved compassionate use treatment, Dr. Kopyov of Celavet and Dr. Wagner of Wyomissing Animal Hospital, came up with a technique that involved injection of the cells in a circular pattern around the rim of each pad, and then applied scaffolding to hold the cells in place and give them a surface for attachment. The paws were then wrapped and bandaged. Dr. Wagner observed: “almost total restoration, no scar tissue in 5 weeks.”

Celavet is committed to a preclinical study and submitting an Investigational New Animal Drug (INAD) for chronic wounds and burns.

Contact Celavie Biosciences

Changing the Paradigm of Regenerative Medicine and Stem Cell Technology