N E W S R E L E A S E For information contact: Joni Morford, Communicore 714/721-8081 jmorford@communicore.com ORQUEST PRESENTS FIRST ANIMAL DATA ON OSSIGEL¨ FRACTURE HEALING TREATMENT Study Shows Ossigel Accelerates Fracture Healing FOR IMMEDIATE RELEASE......September 9, 1996......Seattle, Wash......Scientists from Orquest, Inc. presented results from an animal study of Orquest's Ossigel¨ fracture treatment at the American Society of Bone and Mineral Research annual meeting today. The results showed that fractures treated with Ossigel healed more quickly than those left untreated. In the study, fractures were created in the fibula (leg bone) of rabbits. The mechanical strength of the healing fractures was measured at 23 and 30 days post- surgery. At 23 days, the mechanical strength of fractures treated with Ossigel was 73 percent greater than the strength of those left untreated. At 30 days, the mechanical strength of treated fractures was 77 percent greater than that of untreated fractures. "Ossigel was shown to accelerate fracture healing by promoting the formation of a strong, healthy fracture callus," said James Poser, Ph.D., Orquest's Vice President for Research and Development. "We are optimistic that Ossigel will be a useful minimally invasive treatment in fracture management." Ossigel is a proprietary bioengineered matrix that combines basic fibroblast growth factor (bFGF) and hyaluronic acid. A single dose of Ossigel is injected into the site of recent fractures to accelerate healing. Hyaluronic acid is a highly biocompatible, elastic, gel-like material found naturally in the body that provides an environment conducive to bone formation. Ossigel combines hyaluronic acid with bFGF, a growth factor that occurs naturally in bone that stimulates the proliferation of cells necessary for vascularization and bone growth. Injection of Ossigel into the site of a fresh fracture stimulates development of the fracture callus, an important event in the early stages of normal fracture healing. Approximately six million bone fractures occur annually in the United States, of which many could benefit from treatment with Ossigel. Fracture healing, even in uncomplicated cases, involves a period of convalescence ranging from two to eight months, during which mobility can be limited to the point where occupational and recreational activities may be impossible. Ossigel is intended to accelerate the healing of fractures, thus reducing the period of convalescence. Orquest plans to file a request to conduct human clinical trials of Ossigel to the U.S. Food and Drug Administration in early 1997. Orquest, Inc., a private company based in Mountain View, Calif., was founded in 1994 with the vision of developing and marketing bioengineered matrices that promote bone and cartilage regeneration in targeted applications. The company's innovative products promote the natural regeneration of bone and cartilage for the treatment of orthopedic conditions related to degeneration, disease, and trauma. Ossigel joins Healos¨--a synthetic bone graft alternative--in Orquest's line of bioengineered matrices for bone regeneration. End of document.