The First Adeno-Associated Viral Gene Therapy for Huntington’s Disease Receives the FDA’s Fast Track Designation
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The First Adeno-Associated Viral Gene Therapy for Huntington’s Disease Receives the FDA’s Fast Track Designation

  A recent article in globenewswire.com news reported that the FDA has approved Fast Track Designation for AMT 130, an experimental gene therapy for the treatment of Huntington’s disease. The…

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Gene Therapy Could Change Rare Disease Treatment Forever, But Will Anyone be Able to Afford It?
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Gene Therapy Could Change Rare Disease Treatment Forever, But Will Anyone be Able to Afford It?

According to a story from BNN Bloomberg, gene therapies are without a doubt an upcoming advancement in care and treatment for many diseases that have a genetic origin. This includes…

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Pulmonary Hypertension Drugs are Effective for Some Sarcoidosis Patients, Study Says
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Pulmonary Hypertension Drugs are Effective for Some Sarcoidosis Patients, Study Says

According to a story from Pulmonary Hypertension News, many patients with the rare disease sarcoidosis frequently experience lung complications. Included in these complications is pulmonary hypertension, a condition of elevated…

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Phase 3 Myelodysplastic Syndromes Trial Reaches Enrollment Milestone
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Phase 3 Myelodysplastic Syndromes Trial Reaches Enrollment Milestone

According to a story from sectorpublishingintelligence.co.uk, the biopharmaceutical company Onconova Therapeutics, Inc. recently announced that they have successfully surpassed the 75 percent milestone for enrollment in the company's Phase 3…

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Experimental Combination Treatment for Acute Myeloid Leukemia Shows Potential in Early Trial

According to a story from BioPortfolio, the biopharmaceutical company AVEO Pharmaceuticals and the lung cancer diagnostic company Biodesix recently released the results from the Phase Ib clinical trial testing a…

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Experimental Therapy for T-Cell Prolymphocytic Leukemia Earns Orphan Drug Designation
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Experimental Therapy for T-Cell Prolymphocytic Leukemia Earns Orphan Drug Designation

According to a story from Market Screener, the biopharmaceutical company Imbrium Therapeutics LP recently announced that the US Food and Drug Administration (FDA) has given Orphan Drug designation for the…

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Funding Goal Achieved for Pulmonary Arterial Hypertension Clinical Trial
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Funding Goal Achieved for Pulmonary Arterial Hypertension Clinical Trial

According to a story from Euroinvestor, the drug development company Resverlogix Corp. recently announced that it has received the necessary $2.9 million in funding for a Phase 2 clinical trial…

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Study Reveals Combination Therapy for Aggressive, Cancerous Neuroendocrine Tumors
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Study Reveals Combination Therapy for Aggressive, Cancerous Neuroendocrine Tumors

According to a story from EurekAlert!, a recent research study has found that a two part immunotherapy combination treatment has the potential to be a useful treatment for high-grade neuroendocrine…

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