Specialty Pharma Journal Specialty, Precision & Technology
Researchers at Yale University have used gene editing to successfully correct the most common mutation in the gene that causes cystic fibrosis (CF). A multidisciplinary team of Yale researchers developed a novel approach to edit the genetic defect. In order to correct the mutation, the team used synthetic molecules similar …
Breaking News
- FDA Approves Gavreto for the Treatment of Adults with Metastatic RET Fusion-Positive Non-Small Cell Lung Cancer
- Incyte Announces Pivotal GEOMETRY mono-1 Study Results of Capmatinib in Patients with METex14 Metastatic Non-Small Cell Lung Cancer Published in NEJM
- Natera Announces SMART Study Data for Aneuploidy and 22q Unblinded
- Aimmune Agrees to be Acquired by Nestlé Health Science for $2 Billion
- Twist Bioscience Announces Potent SARS-CoV-2 Neutralizing Data from COVID-19 Therapeutic Antibody Program
- Final Analysis of the Observational GioTag Study: Sequential Afatinib and Osimertinib in Patients with EGFR Mutation-Positive NSCLC
- Santhera Exercises Option to Obtain Worldwide Rights to Vamorolone in Duchenne Muscular Dystrophy and All Other Indications
- FDA Approves Onureg, a New Oral Therapy, as Continued Treatment for Adults in First Remission with Acute Myeloid Leukemia
- FDA Accepts Vertex’s sNDA for Trikafta, Symdeko and Kalydeco for Additional CFTR Mutations
- Gilead Sciences and Jounce Therapeutics Announce Exclusive License Agreement for Novel Immunotherapy Program