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Elektrofi is a biotechnology company focused on improving administration for a wide range of medicines including monoclonal antibodies, therapeutic proteins, and other large molecule drugs. Its breakthrough formulation platform enables stabilized, highly concentrated formulations for subcutaneous administration. The company is using this technology to transform therapies that are administered intravenously, and to enhance injectable products by reducing the volume and frequency of dosing. Elektrofi partners with pharmaceutical companies to jointly develop patient-friendly delivery solutions. Headquartered in Boston, the company`s founding team of MIT engineers and scientists are shaping the future of biologics delivery.
Appleton Area Health Services is a Appleton, MN-based company in the Healthcare, Pharmaceuticals, and Biotech sector.
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
Ansun BioPharma is a clinical stage biopharmaceutical company focused on the development of unique host-directed anti-viral therapies for respiratory viruses. Ansun BioPharma has two products in late stage clinical development. Fludase is a first-in-class broad-spectrum investigational therapeutic agent to treat all forms of influenza, including pandemic variants and drug-resistant variants that cannot be treated by any currently approved flu therapies, including H1N1, H5N1 and H7N9. Paradase is an investigational nebulized drug which is designed to target the receptor for parainfluenza viruses and is being evaluated in a Phase 2 trial for the treatment of lower tract parainfluenza infection in immunocompromised patients.
MEI Pharma (Nasdaq: MEIP) is a San Diego-based pharmaceutical company focused on leveraging its extensive development and oncology expertise to identify and advance new therapies for cancer. Our approach to building our pipeline is to license promising cancer agents and create value in programs through development and commercialization, or strategic partnerships, as appropriate. Our portfolio contains four clinical-stage drug candidates, including one candidate in an ongoing global registration trial and another candidate that is anticipated to advance into a registration trial this year. Our drug candidate pipeline includes: Pracinostat, an oral HDAC inhibitor that is in a Phase 3 pivotal study in combination with azacitidine for the treatment of acute myeloid leukemia. Pracinostat is also being evaluated in a clinical study in patients with myelodysplastic syndrome. Pracinostat is licensed to Helsinn Healthcare SA, a Swiss pharmaceutical corporation. ME-401, a selective oral inhibitor of phosphatidylinositol 3-kinase (“PI3K”) delta. ME-401 is anticipated to progress into a single-agent registration study in 2018 for the treatment of adults with relapsed or refractory follicular lymphoma. Voruciclib, an orally administered and selective cyclin-dependent kinase (“CDK”) inhibitor differentiated by its potent in vitro inhibition of CDK9 in addition to CDK6, 4 and 1. Initiation of a Phase I dose-escalation study in patients with relapsed and/or refractory B-cell malignancies after failure of prior standard therapies is scheduled to being in the second calendar quarter of 2018. ME-344, a novel and tumor selective, isoflavone-derived mitochondrial inhibitor drug candidate, has demonstrated evidence of single-agent activity against refractory solid tumors in a Phase I study. In preclinical studies, tumor cells treated with ME-344 resulted in a rapid loss of ATP and cancer cell death. It is currently being evaluated in an investigator-initiated study in combination with the VEGF inhibitor bevacizumab (marketed as Avastin®) in patients with HER2 negative breast cancer.