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InteKrin Therapeutics is a Los Altos, CA-based company in the Healthcare, Pharmaceuticals, and Biotech sector.
Quva is a national provider specializing in health-system pharmacy services, focusing on sterile injectable compounding and advanced data software platforms. The company operates FDA-registered 503B outsourcing facilities that manufacture ready-to-administer compounded sterile pharmaceuticals, serving thousands of hospitals across the United States. Quva adheres to stringent cGMP standards and utilizes automation and integrated technologies to ensure a reliable supply of high-quality medications. Quvas operations are divided into two main divisions. Quva Pharma delivers essential sterile compounded medications, addressing supply chain reliability and medication shortages. Quva BrightStream offers a data analytics platform that aggregates and analyzes healthcare data, providing actionable insights to optimize pharmacy operations. The company emphasizes patient safety, transparent customer service, and a commitment to innovation and quality, making it a trusted partner for health systems and hospital pharmacies.
Epizyme is a clinical stage biopharmaceutical company that discovers, develops and plans to commercialize innovative personalized therapeutics for patients with genetically defined cancers. We systematically identify the genetic alterations that create cancer causing genes, called oncogenes, select patients in whom the identified genetic alteration is found, and then design small molecule therapeutic product candidates to inhibit the oncogene. The clinical development plan for each of our therapeutic product candidates is directed towards patients with a particular genetically defined cancer. Our approach is part of a broader trend towards personalized therapeutics based on first identifying the underlying cause of a disease affecting specific patient populations, applying rational drug design tools to create a therapeutic to inhibit a molecular target in the identified disease pathway, and using a companion diagnostic to select the right patients for treatment. We have built a proprietary product platform that we use to create small molecule inhibitors of a 96-member class of enzymes known as histone methyltransferases, or HMTs. Genetic alterations can result in changes to the activity of HMTs, making them oncogenic. When Epizyme was founded, we recognized that the HMT class of enzymes might contain many potential oncogenes and presented the opportunity to discover, develop and commercialize multiple personalized therapeutics. We have prioritized 20 of the 96 HMTs as attractive targets for personalized therapeutics based on their oncogenic potential. Our two most advanced therapeutic product programs target the HMTs DOT1L (for the treatment of acute leukemias with genetic alterations of MLL) and EZH2 (for a genetically defined subtype of non-Hodgkin lymphoma and solid tumors including INI1-deficient tumors). We believe that our ongoing Phase 1 adult trial for EPZ-5676, targeting DOT1L, is the first clinical trial of an HMT inhibitor. In May 2014, we initiated a Phase 1b clinical trial for EPZ-5676 in pediatric patients with MLL-r leukemia, which is considered to be the last largely untreatable pediatric acute leukemia. We are also conducting a Phase 1/2 clinical trial of EPZ-6438, which is being developed for the treatment of non-Hodgkin lymphoma and solid tumors including INI1-deficient tumors such as synovial sarcoma and malignant rhabdoid tumors, or MRT. We were founded in 2007 and are led by a management team with extensive experience in the pharmaceutical industry. We have entered into therapeutic collaborations with Celgene, Eisai and GSK that have provided us with approximately $184 million in non-equity funding. As of June 30, 2014, we had $232.1 million in cash, cash equivalents and accounts receivables.
Cardiff Oncology, Inc. is a clinical-stage biotechnology company with the singular mission of developing new treatment options for cancer patients in indications with the greatest medical need.
Criada em 1977, são mais de quatro décadas de uma história construída com qualidade, acessibilidade e inovação, sempre com o foco no bem-estar da população brasileira. Sobre a Cimed: Somos uma das maiores farmacêuticas do país. Com mais de 40 anos de história, uma das poucas empresas do setor que permanece totalmente brasileira e independente até hoje. São mais de 600 produtos no catálogo e uma distribuição nacional para mais de 60 mil pontos de vendas. Além disso, a Cimed é líder em todos os setores em que atua. Temos nosso complexo fabril em Pouso Alegre (MG), o centro de distribuição central e a gráfica em São Sebastião da Bela Vista (MG), além de contar com 25 centros de distribuição espalhados pelo país. Com sede administrativa em São Paulo, são cerca de 5 mil colaboradores em todo Brasil. Somos, também, apoiadores do esporte nacional, patrocinando a Confederação Brasileira de Futebol. Projeto +: Mais de 280 mil m², esse é o tamanho do terreno da nova fábrica de sólidos orais da Cimed em Pouso Alegre, no Sul de Minas Gerais, a ser finalizada até 2022. A nova unidade terá aproximadamente 44 mil m² de área construída, fazendo com que a capacidade produtiva da área de sólidos passe de 28 milhões para 40 milhões comprimidos por mês, podendo chegar a 60 milhões. Pesquisa e Desenvolvimento: A Cimed é uma das poucas empresas do setor a ter o seu próprio centro de bioequivalência e a única a realizar todas as etapas de estudo necessárias para o registro de medicamentos genéricos e similares (clínica, analítica e estatística). Tudo isso é feito no Instituto Claudia Marques de Pesquisa e Desenvolvimento (ICM P&D), criado em 2004. Nossos números - Mais de 5 mil colaboradores - Mais de 60 mil pontos de venda - Presentes em mais de 90% das farmácias brasileiras - Cerca de 600 produtos no portfólio