2010年10月,FDA首例核准的胚胎幹細胞臨床試驗,治療脊髓損傷的病患在美國亞特蘭大的Shepherd中心開始進行.芝加哥的西北大學也於後續開始進行病人的蒐集,成為第二個臨床試驗的參與機構.而加州的史丹佛大學於1月24日宣布,將成為第三個醫療機構參與此項胚胎幹細胞的臨床試驗.
這項臨床試驗是由傑龍公司(Geron)所發起與執行,利用胚胎幹細胞誘導成寡狀樹突的前驅神經細胞(Oligodendrocyte precursors),再打入脊髓損傷的病患,首要目標是進行病患安全試驗的評估.
史丹佛大學的第一期臨床試驗對象為10名病患,其條件為兩個星期內首次的脊髓受損患者或是近期的創傷經醫師評估後被推薦的病患.
手術的流程為:由Geron公司製造並提供前驅神經細胞(GRNOPC1),送至史丹佛大學實驗室進行解凍與處理準備,最後在合作醫院-聖克拉拉醫療中心(Santa Clara Valley Medical Center:SCVMC)進行移植試驗.
SCVMC醫療中心為西岸最大的神經損傷治療與復健中心,每年有150名病患因車禍,摔落,運動等意外造成嚴重的脊髓損傷.參與此項臨床試驗的史丹佛大學教授-Gary Steinberg也是醫療中心的神經科醫師,將為病患進行這次的移植手術.
Steinberg表示,過去對於中風,腦瘤和阿茲海默症等的脊髓損傷,神經的修復與再生是不抱有任何希望,但是現在幹細胞研究已走向臨床試驗,跳脫過去限有的動物實驗結果,直接進行人體移植作觀察,對未來醫療是個很大的進展.
第一期的人體試驗安全評估結果如果順利,下一步目標是就是要達到神經修復的療效,希望未來脊髓損傷的患者能再站起來,迎向新的人生.
Stanford joins first embryonic-stem-cell therapy clinical trial
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The first clinical trial of cells derived from human embryonic stem cells began in October 2010 in a paralyzed patient at the Shepherd Center in Atlanta. Today, Stanford University School of Medicine and Santa Clara Valley Medical Center became the third site to participate in the trial, which will enroll up to 10 patients with spinal cord injuries at up to seven institutions nationwide. |
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(Media-Newswire.com) - The first clinical trial of cells derived from human embryonic stem cells began in October 2010 in a paralyzed patient at the Shepherd Center in Atlanta. Today, Stanford University School of Medicine and Santa Clara Valley Medical Center became the third site to participate in the trial, which will enroll up to 10 patients with spinal cord injuries at up to seven institutions nationwide. The FDA-approved, phase-1 trial is meant to test only the safety of the cells, which can develop into neural support cells called oligodendrocytes found in the brain and central nervous system. If the investigational treatment is shown to be safe for use in humans, larger clinical trials will be designed to test whether the cells are better able than conventional treatments to improve a patient’s condition. Because the cells must be administered within two weeks of the initial spinal cord injury, the trial is open only to those with very recent trauma and only upon physician referral. The trial is run by Menlo Park-based Geron Corp., which developed and manufactures the cells for testing. The cells for this portion of the trial will be thawed and prepared at Stanford, and the surgery to implant the cells will take place at Valley Medical Center, which is one of the largest referral centers for acute spinal cord injury and rehabilitation on the West Coast. Physicians certified to conduct the procedure include Stanford neurosurgeons Gary Steinberg, MD, PhD, and Marco Lee, MD, PhD. Steinberg is the principal investigator of the Stanford/SCVMC portion of the trial. He has been researching the use of stem cells in models of neurological injury or illness for more than a decade, and he heads a team of Stanford researchers that received a $20 million grant from the California Institute for Regenerative Medicine to study how neural stem cells could be used to treat people with ischemic stroke — a condition that occurs when a portion of the brain is deprived of blood flow. “Until recently, we have not had any hope of restoring neurological function in people with spinal cord injury or stroke, or those with brain tumors or Alzheimer’s disease,” said Steinberg, the Bernard and Ronni Lacroute-William Randolph Hearst Professor in Neurosurgery and Neurosciences. “But now we’re moving stem cell therapy into the clinic, which I feel is a tremendously important step. People are not mice or rats, and we can learn so much from clinical trials that we can never learn by studying animals.” Steinberg and Stanford have a strong background in stem cell biology, while Santa Clara Valley Medical Center has the patients and an extensive rehabilitation facility for spinal cord injuries. “Valley Medical Center treats more than 150 people a year with severe spinal cord trauma, many of which are caused by motor vehicle accidents, falls and sports injuries. Patients with this kind of injury are very familiar to our staff, and we have the training and experience to help them through their recovery,” said Stephen McKenna, MD, chief of SCVMC’s Rehabilitation Trauma Center. “By collaborating with Stanford, we can evaluate and enroll patients in the trial without altering their normal referral pathway.” During the procedure, the neurosurgeon will apply about 2 million of the special cells ( called GRNOPC1 ) directly into the injured area of the enrolled patient’s spinal cord. Following the surgery at Santa Clara Valley Medical Center, the patient will enter an intensive inpatient rehabilitation program under the supervision of specialists in spinal cord injury medicine. Researchers will then monitor the patient to confirm that the cells are safe for use in humans. The oligodendrocyte precursors ( GRNOPC1 ) are produced from stem cells that were originally derived from a single embryo created through in vitro fertilization. Such excess embryos are usually discarded when no longer needed, but can be donated for research by the parents under informed consent. The U.S. Food and Drug Administration approved the human clinical trial in 2009 after extensive tests in laboratory animals. The first patient was treated in October at the Shepherd Center in Atlanta; Northwestern University in Chicago is also open for patient enrollment. Other participating sites have not yet been identified.
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